Thank you to Dr. L Bozhilova for advice on the statistical analysis of droplet generation PCR data. Thank you to Dr. H Zhang for providing the oocytes used to generate data in Figure&#160;3C and Figure&#160;4B. This work was carried out by SPB at the Medical Research Council Mitochondrial Biology Unit (MC_UU_00015/9), University of Cambridge, and funded by&#160;a Wellcome Trust Principal Research Fellowship held by PFC (212219/Z/18/Z).

All experiments followed the ARRIVE guidelines and were approved by the University of Cambridge Animal Welfare Ethical Review Body (AWERB).
NOTE: All sample preparation steps prior to droplet generation must be performed in a clean pre-PCR work area, ideally in a UV-sterilized cabinet where possible. The protocol described here uses specific droplet generation PCR equipment (see Table of Materials), and while the general method should be applicable to other systems, it is recommended to consult the manufacturer&#39;s guidelines regarding primer/probe concentrations, PCR cycling conditions, etc., as they may differ from those described here. Cell lines/primary cells used in this study were as follows: Human HeLa cells (commercially obtained), human HEK 293T cells (commercially obtained), primary human dermal fibroblast cells (obtained from the Newcastle Biobank), human cybrids (WT &#38; &#916;H2.1 deletion15, obtained from C. Moraes, University of Miami), mouse embryonic fibroblasts (immortalized, from C57Bl/6 mice, obtained from J. Stewart, Newcastle University), mouse primordial germ cells (obtained from C57Bl/6 mouse embryos), and mouse MII oocytes (obtained from adult female C57Bl/6 mice). All cultured cells were maintained in High Glucose (4.5g/L) DMEM supplemented with 10% fetal bovine serum at 37 &#176;C with 5% CO2. Primary mouse cells used in this study were isolated from animals kept according to the Animal (Scientific Procedures) Act 1986 under Home Office Project License P6C97520A.
1. Design and synthesize primer &#38; probe sets targeting DNA sequences of interest
NOTE: Droplet generation PCR can also be performed using a dsDNA binding dye in place of the amplicon-specific probes.
<ol>
	<li>Design the primer and probe sequences according to the guidelines given by the system manufacturer. Validated primer and probe sequences suitable for measuring single-cell mtDNA copy number/deletion heteroplasmy in both human16,17 and mouse18 cells are provided in Table 1. When selecting alternative target sequences, consider the following points.
	<ol>
		<li>Multiplex two primer/probe sets in a single PCR assay but ensure that the two assays utilize one FAM-labeled probe and one HEX-labeled probe so that the target amplicons can be differentiated by the droplet reader. This protocol presents a duplex probe assay. With careful experimental design, multiplexing can be increased up to four targets, and alternative platforms can achieve higher-dimensional multiplexing.</li>
		<li>When multiplexing primer/probe sets targeting separate mtDNA sequences, ensure that the amplicons generated by the two primer sets do not overlap.</li>
		<li>When measuring heteroplasmy in samples carrying mtDNA deletions, ensure that one target amplicon falls within the expected deleted region and the other falls outside of the expected deleted region. 
		NOTE: Optimal PCR cycling conditions for alternative assays may differ from those quoted in Step 5.1; see the Discussion for further details on assay optimization.</li>
	</ol>
	</li>
</ol>
2. Isolation of DNA from single cells
NOTE: This method can also be used for small bulk samples of up to 100 cells.
<ol>
	<li>Collect single cells using an appropriate method, such as Fluorescence-Activated Cell Sorting (FACS)19 or laser capture microdissection20, in as small a volume as possible into a suitable receptacle (e.g., 96-well plate). Use of a cell viability dye prior to or during single-cell isolation will minimize the likelihood of isolating dead cells. Sort the single cells directly into lysis buffer if desired and store at -80 &#176;C (up to 6 months) prior to analysis.</li>
	<li>Lyse the cells in a small volume (&#60;10 &#181;L) of a suitable lysis buffer (the buffer used in this study is described in step 2.2.1.). 
	NOTE: All data obtained from cells in this study are from single-cell lysates or pools of 20 cells (sample sizes are stipulated in the figure legends). Efficient formation of an oil/droplet emulsion during the droplet generation step of the droplet generation PCR protocol can be significantly affected by the presence of detergents in the sample; therefore, it is recommended to validate the compatibility of all cell-lysis buffers with droplet generation at the intended input concentration before proceeding with experimental samples and using the smallest practical volume of lysis buffer. The following lysis protocol results in minimal impact on droplet generation efficiency.
	<ol>
		<li>Prepare the lysis buffer containing 50 mM Tris-HCl pH 8.3, 1% TWEEN-20, and 200 &#181;g/mL Proteinase K.</li>
		<li>Add 2.5 &#181;L of the lysis buffer to each sample, seal the plate with an adhesive plate seal, and then centrifuge the samples at 1,000 x g for 1 min at 4 &#176;C.</li>
		<li>Incubate the samples at 37 &#176;C for 30 min on the thermocycler with the heated lid set at 105 &#176;C to prevent the condensation of liquid on the plate cover.</li>
		<li>Add 7.5 &#181;L of nuclease free water to each sample to get a final sample volume of 10 &#181;L, re-seal the plate, and then centrifuge the samples at 1,000 x g for 1 min at 4 &#176;C.</li>
		<li>Incubate on the thermocycler at 80 &#176;C for 15 min (heated lid set to 105 &#176;C) to inactivate Proteinase K.</li>
		<li>Centrifuge the samples at 1,000 x g for 1 min at 4 &#176;C and then keep on ice.</li>
	</ol>
	</li>
	<li>Proceed to step 3 below. 
	NOTE: Cell lysates can be stored at -20 &#176;C prior to continuing with step 3; however, use freshly eluted DNA where possible to eliminate the risk of freeze-thaw cycles resulting in DNA degradation.</li>
</ol>
3. Preparation of samples
NOTE: Ensure that technical replicates of samples and non-template controls (NTCs) are included on each assay plate to ensure the accuracy of results. The dynamic range of the droplet generation PCR assay is up to 120,000 copies of the target amplicon per reaction. For single-cell or small bulk-cell sample lysates, dilution is unlikely to be necessary, and the lysate mixture can be input directly to the reaction for the measurement of mtDNA copy number (e.g., a lysate sample of 10 &#181;L can be split and run in triplicate with 3 &#181;L input directly into each assay). However, using undiluted lysate from cells with very high copy mtDNA numbers (e.g., oocytes) or containing larger numbers of cells (e.g., 50-100) may exceed this dynamic range. In such cases, an initial serial dilution is required to identify an appropriate dilution factor that avoids saturation of the assay for that specific cell type/cell number (see Representative Results for further details).
<ol>
	<li>Defrost all reagents on ice, vortex, and spin down briefly before use.</li>
	<li>Prepare the master mix (minus sample DNA) on ice as described in (Table 2). 
	NOTE: If only one target amplicon is being measured, add an additional 2.55 &#181;L of nuclease-free water per sample to achieve the final volume of 22 &#181;L. Prepare sufficient master mix for the number of samples and NTCs to be analyzed, plus enough to account for any &#39;blank&#39; wells required on the droplet generation PCR plate (see next step).</li>
	<li>Vortex the prepared master mix briefly to mix and aliquot the required volume (22 &#181;L minus input DNA volume) into each well of a droplet generation PCR 96-well plate. Arrange the samples in full columns on the 96-well plate; fill any empty wells in incomplete columns with master mix and use them as NTCs.</li>
	<li>Add the input DNA to each sample well and nuclease-free water/elution buffer to NTC wells to bring the total volume of each up to 22 &#181;L.</li>
	<li>Seal the plate with an adhesive plate seal and place on a shaker at 2,000 rpm for 1 min, and then centrifuge at 1,000 x g for one min at 4 &#176;C.</li>
	<li>Place the plate on ice and proceed to Step 4. 
	NOTE: Prepared plates can be stored on ice and protected from light for short periods of time (e.g., 1-2 h) before proceeding with droplet generation.</li>
</ol>
4. Generation of droplets
NOTE: Refer to Figure 1A for the schematic of the droplet generator instrument deck referenced in this section.
<ol>
	<li>Power on the droplet generator.</li>
	<li>Check that a bottle of droplet generating oil is loaded to position E of the instrument deck. If prompted, follow the on-screen instructions to replace the bottle.</li>
	<li>Click Configure Sample Plate on the touch screen. Select all columns on the sample plate that contain samples/blanks. 
	NOTE: Entry of plate name and details of the experiment at this step is optional and not required to continue setting up the experiment.</li>
	<li>Click OK to confirm the plate configuration; orange lights will illuminate on the instrument deck to indicate positions where consumables need to be loaded.</li>
	<li>Load the droplet generator cartridges to position B on the instrument deck so that all lights turn green.</li>
	<li>Place an empty tip waste trough into position C on the instrument deck.</li>
	<li>Remove lids from filter tip boxes and load to position D on the instrument stage so that all lights turn green.</li>
	<li>Remove the adhesive plate seal from the sample plate and load to position F of the instrument deck so that the light turns green.</li>
	<li>Place an empty droplet collection 96-well plate into a cool block (pre-chilled at -20 &#176;C) and load to position G of the instrument deck so that the light turns green.</li>
	<li>Click Start Droplet Generation on the instrument touch screen.</li>
	<li>Click Start Run on the instrument touch screen. The instrument lid will close automatically. After initializing, the time remaining until droplet generation is complete will display on the instrument touch screen.</li>
	<li>Once the droplet generation is complete, check the sample collection plate visually to confirm that a droplet emulsion layer is present above the oil phase in each well (Figure 1B). 
	NOTE: If a droplet emulsion layer is not visible, do not proceed further with the experiment and check for any errors that may have occurred during previous steps of the protocol.</li>
	<li>Clear the used consumables from the instrument deck and empty the tip-waste trough.</li>
	<li>Power on the plate sealer, set the temperature to 180 &#176;C and seal time to 5 s, and allow the machine to reach the operating temperature.</li>
	<li>Put the sample collection plate into the plate sealer plate-holder and place a fresh foil seal on top of the plate with the red line facing upwards. Take care not to touch the underside of the foil seal. 
	NOTE: The plate holder should be stored at room temperature (RT) and only placed into the plate sealer drawer when a foil seal is being applied to prevent heat transfer to the sample collection plate.</li>
	<li>When the plate sealer has reached operating temperature, press Eject on the instrument touchscreen; the drawer will open automatically.</li>
	<li>Place the plate holder into the plate sealer drawer and press Seal. The drawer will close automatically and then open again once sealing is complete.</li>
	<li>Replace the sealed plate on the cold block, turn off the plate sealer, and proceed immediately to Step 5. 
	NOTE: At this stage, the droplets are unstable, so ensure that the PCR step is commenced within 1 h of droplet generation finishing.</li>
</ol>
5. PCR
<ol>
	<li>Place the sealed droplet collection plate onto a PCR cycler equipped with a 96-deep-well block and run the thermal cycling protocol described in Table 3. 
	NOTE: Set heated lid temperature to 105 &#176;C and sample volume to 40 &#181;L. Denaturation and annealing/extension steps must include a temperature ramp-rate of 2 &#176;C/s to ensure that the oil has time to equilibrate to the correct temperature.</li>
	<li>Proceed to Step 6. 
	NOTE: Once the thermal cycling protocol is complete, the droplets are more stable, and the plate can be stored for up to 4 days at 4 &#176;C before proceeding with the next step.</li>
</ol>
6. Droplet reading
<ol>
	<li>Power on the droplet reader and connected computer.</li>
	<li>Check the fluid levels in the droplet reader oil and droplet reader waste bottles and fill/empty these, respectively, if required.</li>
	<li>Load the plate containing the post-PCR samples into the droplet reader plate holder, place the cover on top of the holder and secure it in place with the black locking clips. Do not remove the foil lid from the sample plate.</li>
	<li>Press the Open/Close button on the lid of the droplet reader to open it.</li>
	<li>Load the droplet reader plate holder containing the sample plate into the reader chamber and locate it securely onto the magnetic base.</li>
	<li>Press the Open/Close button on the lid of the droplet reader to close it.</li>
	<li>Open the analysis software interface, select the Add Plate tab and prepare a new sample plate as follows:
	<ol>
		<li>Click Add Plate and then Configure Plate.&#160;</li>
		<li>In the Plate Information tab enter a Plate Name, select Supermix for Probes (no dUTP) from the Supermix drop-down menu and enter a file name under Save Data File As.</li>
		<li>In the Well Selection tab highlight the wells to be analyzed and click Include Selected Wells. 
		NOTE: Steps 6.7.4 &#8211; 6.7.7 are optional.</li>
		<li>In the Well Information tab, select the wells to be annotated. 
		NOTE: Refer to Figure 1D&#160;for an example of the Well Information tab interface.</li>
		<li>Select Direct Quantification (DQ) from the Experiment Type drop-down menu, populate the Sample Description, Sample Type &#38; Target Name boxes, and add Well Notes and/or Plate Notes as required.</li>
		<li>Click Apply. The information in the fields will be applied to the selected wells.</li>
		<li>Repeat steps 6.7.4&#8211;6.7.6 until all sample wells have been annotated.&#160;</li>
	</ol>
	</li>
	<li>Once the plate configuration is complete, click Start Run.</li>
	<li>When the run is complete, discard the empty sample plate and empty the droplet reader waste bottle if necessary.&#160;</li>
	<li>Proceed to Step 7.</li>
</ol>
7. Analysis of results
NOTE: The droplet reader measures the fluorescence intensity in the FAM and HEX channel for each droplet in a sample. In a successful assay, droplets fall into one of two categories for each probe: Negative (meaning the target was not present in the droplet) or Positive (meaning the target was present in the droplet). Prior to analyzing samples, ensure that each well contains &#62;10,000 droplets and has two clearly separate populations of low fluorescence (negative) and high fluorescence (positive) droplets in each channel (Figure 2A).
<ol>
	<li>Select the Data Analysis tab and open the file to be analyzed from the My Datafiles menu.</li>
	<li>Click the 1D Amplitude tab for single-color experiments or the 2D Amplitude tab for two-color experiments.</li>
	<li>Apply a fluorescence threshold to each channel to differentiate the positive and negative droplets. The analysis software will attempt to apply an automatic threshold on a sample-by-sample and channel-by-channel basis, but if this appears to have failed, or looks inaccurate, then manually apply the threshold as follows:
	<ol>
		<li>Select the wells that require thresholding.</li>
		<li>Manually apply the threshold in the clear space between the positive and negative populations on the amplitude plot using the Threshold Line Mode tool. When setting manual thresholds in 2D view, ensure that the crosshair is placed so that the four droplet populations (double negative, single positive FAM, single positive HEX, and double positive) are clearly separated. 
		NOTE: Thresholding can either be done well-by-well or applied to multiple wells at once.</li>
	</ol>
	</li>
	<li>Once all samples have had a threshold applied, export the results as a .csv file for further analysis by clicking on the Data Table tab, clicking Import/Export and selecting Export Visible Data to CSV. Enter a suitable file name and click Save.</li>
	<li>Calculate the mtDNA copy number in the initial sample as follows: 
	Copy Number = mtDNA target concentration&#160;&#215; 22&#160;&#215; 1/fraction of total lysate input 
	NOTE: If two mitochondrial probes are used, then the concentration of the two targets is averaged before making the calculation. For samples containing more than one cell, the copy number per cell is calculated by dividing by the number of cells in the sample. It is important to use the &#39;Concentration&#39; value (i.e., number of copies per microliter) multiplied by the initial sample volume of 22 &#181;L, rather than the &#39;Copies per 20 &#181;L&#39; value calculated in the .csv file, since the mtDNA copies left in the 2 &#181;L overage required by the droplet generator must be taken into account when calculating the absolute copy number of the initial sample.</li>
	<li>For cells carrying heteroplasmic mtDNA deletions, calculate the copy number using the results from the mtDNA target outside the deleted region (i.e., the target present in both deleted and WT mtDNA molecules). The deletion heteroplasmy is calculated using the concentrations of the target inside the deleted region and the target outside the deleted region as follows: 
	<img alt="Equation 1" src="/files/ftp_upload/63870/63870eq01.jpg" style="margin: auto;" /></li>
</ol>

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P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=PCR+based+determination+of+mitochondrial+DNA+copy+number+in+multiple+species.">PCR based determination of mitochondrial DNA copy number in multiple species.</a> Methods in Molecular Biology. 1241, 23-38 (2015).</li><li>Kamitaki, N., Usher, C. L., McCarroll, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Using+droplet+digital+PCR+to+analyze+allele-specific+RNA+expression.">Using droplet digital PCR to analyze allele-specific RNA expression.</a> Methods in Molecular Biology. 1768, 401-422 (2018).</li><li>Maeda, R., Kami, D., Maeda, H., Shikuma, A., Gojo, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High+throughput+single+cell+analysis+of+mitochondrial+heteroplasmy+in+mitochondrial+diseases.">High throughput single cell analysis of mitochondrial heteroplasmy in mitochondrial diseases.</a> Scientific Reports. 10 (1), 10821 (2020).</li><li>Quan, P. L., Sauzade, M., Brouzes, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=dPCR:+A+Technology+Review.">dPCR: A Technology Review.</a> Sensors (Basel). 18 (4), (2018).</li><li>Lin, X., Huang, X., Urmann, K., Xie, X., Hoffmann, M. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Digital+loop-mediated+isothermal+amplification+on+a+commercial+membrane.">Digital loop-mediated isothermal amplification on a commercial membrane.</a> ACS Sensors. 4 (1), 242-249 (2019).</li><li>Li, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fully+integrated+microfluidic+devices+for+qualitative,+quantitative+and+digital+nucleic+acids+testing+at+point+of+care.">Fully integrated microfluidic devices for qualitative, quantitative and digital nucleic acids testing at point of care.</a> Biosensors and Bioelectronics. 177, 112952 (2021).</li></ol>

No conflicts of interest to disclose.

The protocol described here is applicable across a wide range of cell types and species in addition to those discussed above, although careful optimization of new assay designs will be key to ensure that accuracy and repeatability of the method are maintained when moving away from previously validated primer/probe combinations. When working with single cells it is vital to ensure that sample collection is performed as accurately as possible (e.g., using stringent single-cell parameters when sorting cells by FACS) to ensu...

Mammalian mitochondrial (mt)DNA is a small (approx. 16.5 Kb), circular DNA genome residing in the mitochondrial matrix that encodes 37 genes, comprising two rRNAs, 22 tRNAs, and 13 protein-coding genes1. Unlike the nuclear genome, which contains one (haploid) or two (diploid) copies of each gene per cell, mtDNA is present in multiple copies in the mitochondria of each cell, ranging from tens of copies (e.g., mature spermatocytes) to hundreds of thousands of copies (e.g., oocytes)2,3. A consequence of this multi-copy nature is that mutations in the mtDNA genome, which may exist as single-nucleotide polymorphisms (SNPs), deletions, or duplications, can be present at varying levels in any given cell, making up anywhere from 0% to 100% of the cell's total mtDNA population. The existence of wild-type and mutant mtDNA genomes in the same cell is termed heteroplasmy, and pathogenic heteroplasmic mtDNA mutations are a major cause of mitochondrial disease, with several common neurological syndromes linked to underlying heteroplasmic mtDNA mutations4.
Two key parameters that contribute to the likelihood of a heteroplasmic mtDNA mutation causing clinical disease are the heteroplasmy level and the mtDNA copy number. Many heteroplasmic mutations display a threshold effect, with biochemical and clinical phenotypes only becoming apparent above a certain heteroplasmy level, typically around 80%5, and subsequently worsening as heteroplasmy increases further4. However, it is also important to consider the number of copies of mtDNA present in the cell, as this will influence the number of wild-type (i.e., 'healthy') mtDNA genomes that are present at a given heteroplasmy level. Studies in mitochondrial disease patients have highlighted the importance of this interplay between heteroplasmy and copy number5,6, and Filograna et al. recently reported an increase in mtDNA copy number alleviating symptoms despite unchanged heteroplasmy in a mouse model of mitochondrial disease7.
Whilst much has been done in recent years to improve the understanding of the pathogenesis and transmission of diseases caused by mtDNA heteroplasmy, most of this work has been conducted at the level of tissues rather than cells, comparing mean tissue heteroplasmy levels and copy number measurements acquired from bulk tissue biopsies and blood samples. Some well-established techniques, such as laser capture microdissection, allow for such measurements at the cellular level8,9; however, the recent explosion of high-throughput single-cell analysis methods, or so-called "Single-cell Omics"10, has created a requirement for methods that can accurately measure these crucial mtDNA parameters at the single-cell level.
The droplet generation PCR method takes advantage of recent advances in microfluidic technology to improve upon existing methods of quantitating unknown DNA concentrations via PCR amplification of specific target amplicons in the sample DNA11. Unlike qPCR, where the sample DNA is amplified in a single reaction, with the relative rate of accumulation of PCR product acting as the readout, this method splits the initial sample into thousands of individual droplets, thus compartmentalizing the sample DNA molecules into spatially separate reactions12. The subsequent PCR reaction proceeds in each individual droplet, with the PCR product only accumulating in droplets that contain the target DNA. The result of this reaction is a digital output in the form of a pool of droplets that either contain a copy of the target DNA and amplified PCR product, or do not contain target DNA. Using fluorescent DNA probes or a double-stranded (ds)DNA binding dye, the droplets containing amplified product can be counted, and the ratio of 'positive' to 'negative' droplets can be used to calculate the absolute number of DNA copies that were present in the initial sample. This absolute measurement, as opposed to the relative measurement acquired from a qPCR reaction, is the key factor that allows this methodology to be used for accurate measurement of mtDNA copy number and heteroplasmy in single cells11, and several recent studies have already utilized droplet generation PCR technology for this purpose13,14. This article presents a method for measuring mtDNA copy number and deletion heteroplasmy in single cells from both human and mouse tissue.

<table><tbody><tr><td>50% Tween-20 solution</td><td>Novex</td><td>3005</td><td></td></tr><tr><td>Automated droplet-generating oil&amp;nbsp;</td><td>Bio Rad</td><td>1864110</td><td>Commercial oil formulation used to generate the oil/droplet emulsion (used in Protocol Step 4.1)</td></tr><tr><td>C1000 PCR machine with deep-well block</td><td>Bio Rad</td><td>1851197</td><td>PCR thermocycler equipped with a deep-well heating block, used for cell lysis (Protocol Step 2.1.2.) and PCR cycling (Protocol Step 5)</td></tr><tr><td>Collection plate cooling block</td><td>Bio Rad</td><td>12002819</td><td>Cooling block that keeps samples chilled during droplet generation (used in Protocol step 4.3)</td></tr><tr><td>ddPCR 96-well plates&amp;nbsp;</td><td>Bio Rad</td><td>12001925</td><td>96-well plates pipet tips designed for use in the QX200 AutoDG droplet generator, used for sample preparation (Protocol step 3.4) and droplet collection (Protocol step 4.3)</td></tr><tr><td>ddPCR droplet reader oil&amp;nbsp;</td><td>Bio Rad</td><td>1863004</td><td>Commercial oil formulation used by the droplet reader (used in Protocol step 6.1)</td></tr><tr><td>ddPCR Supermix for Probes (no dUTP)</td><td>Bio Rad</td><td>1863023</td><td>Commercial supermix for use in ddPCR experiments utilising probes (used in Protocol Step 3.3)</td></tr><tr><td>DG32 automated droplet generator cartridges&amp;nbsp;</td><td>Bio Rad</td><td>1864108</td><td>Microfluidic cartridges used in the QX200 AutoDG droplet generator to generate the oil/droplet emulsion (used in Protocol Step 4.3)</td></tr><tr><td>Fetal bovine serum</td><td>Gibco</td><td>10270-106</td><td>Qualified fetal bovine serum</td></tr><tr><td>Foil plate covers&amp;nbsp;</td><td>Bio Rad</td><td>1814040</td><td>Foil plate covers used to seal droplet collection plates after droplet generation (used in Protocol step 4.6)</td></tr><tr><td>HEK 293T cells</td><td>Takara</td><td>632180</td><td>Commercial subclone of the transformed human embryonic kidney cell line, HEK 293, expressing the SV40 Large-T antigen</td></tr><tr><td>HeLa cells</td><td>ECACC</td><td>93021013</td><td>Human cervix epitheloid carcinoma cells</td></tr><tr><td>High glucose DMEM</td><td>Gibco</td><td>13345364</td><td>4.5g/L D-Glucose, with L-glutamine and sodium pyruvate</td></tr><tr><td>Human cybrids</td><td>University of Miami</td><td></td><td></td></tr><tr><td>Mouse embryonic fibroblasts&amp;nbsp;</td><td>Newcastle University</td><td>Immortalized from C57Bl/6 mice</td><td></td></tr><tr><td>Nuclease-free water</td><td>Ambion</td><td>AM9937</td><td></td></tr><tr><td>PCR plate seals</td><td>Pierce</td><td>SP-0027</td><td>Clear adhesive plate seals, only used pre-droplet generation (foil seal must be used in step 4.6)</td></tr><tr><td>Pipet Tip Waste Bins</td><td>Bio Rad</td><td>1864125</td><td>Disposable collection bin used to collect discarded tips in the QX200 AutoDG droplet generator (used in Protocol step 4.3)</td></tr><tr><td>Pipet tips for AutoDG system&amp;nbsp;</td><td>Bio Rad</td><td>1864120</td><td>Filtered pipet tips designed for use in the QX200 AutoDG droplet generator (used in Protocol step 4.3)</td></tr><tr><td>Primary human dermal fibroblast cells</td><td>Newcastle Biobank</td><td></td><td></td></tr><tr><td>Primers/Probes</td><td>IDT</td><td>N/A</td><td>Exact primer/probe sequences will be assay dependent. Primers and probes used in this study are given in Table 1</td></tr><tr><td>Proteinase K 20 mg/mL solution</td><td>Ambion</td><td>AM2546</td><td></td></tr><tr><td>PX1 PCR plate sealer</td><td>Bio Rad</td><td>1814000</td><td>Applies foil seals to ddPCR sample plates after droplet generation (used in Protocol Step 4.6)</td></tr><tr><td>QX Manager software</td><td>Bio Rad</td><td>12012172</td><td>Droplet reader set up &amp;amp; analysis software (used in Protocol Steps 6 &amp;amp; 7)</td></tr><tr><td>QX200 AutoDG droplet generator</td><td>Bio Rad</td><td>1864101</td><td>Automated microfluidic droplet generator (used in Protocol Step 4)</td></tr><tr><td>QX200 droplet reader</td><td>Bio Rad</td><td>1864003</td><td>Droplet reader (used in Protocol Step 6)</td></tr><tr><td>Trizma pre-set crystals pH 8.3</td><td>Sigma</td><td>T8943-100G</td><td></td></tr></tbody></table>

measuring single-cell mitochondrial dna copy number and heteroplasmy using digital droplet polymerase chain reaction

The mammalian mitochondrial (mt)DNA is a small, circular, double-stranded, intra-mitochondrial DNA molecule, encoding 13 subunits of the electron transport chain. Unlike the diploid nuclear genome, most cells contain many more copies of mtDNA, ranging from less than 100 to over 200,000 copies depending on cell type. MtDNA copy number is increasingly used as a biomarker for a number of age-related degenerative conditions and diseases, and thus, accurate measurement of the mtDNA copy number is becoming a key tool in both research and diagnostic settings. Mutations in the mtDNA, often occurring as single nucleotide polymorphisms (SNPs) or deletions, can either exist in all copies of the mtDNA within the cell (termed homoplasmy) or as a mixture of mutated and WT mtDNA copies (termed heteroplasmy). Heteroplasmic mtDNA mutations are a major cause of clinical mitochondrial pathology, either in rare diseases or in a growing number of common late-onset diseases such as Parkinson's disease. Determining the level of heteroplasmy present in cells is a critical step in the diagnosis of rare mitochondrial diseases and in research aimed at understanding common late-onset disorders where mitochondria may play a role. MtDNA copy number and heteroplasmy have traditionally been measured by quantitative (q)PCR-based assays or deep sequencing. However, the recent introduction of ddPCR technology has provided an alternative method for measuring both parameters. It offers several advantages over existing methods, including the ability to measure absolute mtDNA copy number and sufficient sensitivity to make accurate measurements from single cells even at low copy numbers. Presented here is a detailed protocol describing the measurement of mtDNA copy number in single cells using ddPCR, referred to as droplet generation PCR henceforth, with the option for simultaneous measurement of heteroplasmy in cells with mtDNA deletions. The possibility of expanding this method to measure heteroplasmy in cells with mtDNA SNPs is also discussed.

Following droplet generation, a clear layer of opaque droplets is visible floating on top of the oil phase in each well (Figure 1B). Droplet formation can be adversely affected by the presence of detergents in the input lysate when performing experiments on single cells. Using the lysis protocol described in 2.1.2., droplet yields above the recommended level of 10,000 are routinely achieved, despite the presence of a small residual amount of TWEEN-20 in the final sample (<strong class="xfig"...

Watch this Scientific Journal Video about Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction at JoVE.com

Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction

Here we present a protocol for measuring absolute mitochondrial (mt)DNA copy number and mtDNA deletion heteroplasmy levels in single cells.

The mammalian mitochondrial (mt)DNA is a small, circular, double-stranded, intra-mitochondrial DNA molecule, encoding 13 subunits of the electron ...

measuring-single-cell-mitochondrial-dna-copy-number-heteroplasmy

Universidad de Cartagena UDEC

Research

JoVE Journal

Medicine

4.5K Views.  University of Cambridge, Cambridge Biomedical Campus. Here we present a protocol for measuring absolute mitochondrial (mt)DNA copy number and mtDNA deletion heteroplasmy levels in single cells. 

Video: Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction

Methodology for Accurate Detection of Mitochondrial DNA Methylation

Quantification of DNA methylation can be achieved using bisulfite sequencing, which takes advantage of the property of sodium bisulfite to convert unmethylated cytosine into uracil, in a single-stranded DNA context. Bisulfite sequencing can be targeted (using PCR) or performed on the whole genome and provides absolute quantification of cytosine methylation at the single base-resolution. Given the distinct nature of nuclear- and mitochondrial DNA, notably in the secondary structure, adaptions of bisulfite sequencing methods for investigating cytosine methylation in mtDNA should be made. Secondary and tertiary structure of mtDNA can indeed lead to bisulfite sequencing artifacts leading to false-positives due to incomplete denaturation poor access of bisulfite to single-stranded DNA. Here, we describe a protocol using an enzymatic digestion of DNA with BamHI coupled with bioinformatic analysis pipeline to allow accurate quantification of cytosine methylation levels in mtDNA. In addition, we provide guidelines for designing the bisulfite sequencing primers specific to mtDNA, in order to avoid targeting undesirable NUclear MiTochondrial segments (NUMTs) inserted into the nuclear genome.

Here, we present a protocol to allow accurate quantification of mitochondrial DNA (mtDNA) methylation. In this protocol, we describe an enzymatic digestion of DNA with BamHI coupled with a bioinformatic analysis pipeline which can be used to avoid overestimation of mtDNA methylation levels caused by the secondary structure of mtDNA.

Quantification of DNA methylation can be achieved using bisulfite sequencing, which takes advantage of the property of sodium bisulfite to convert ...

Genetics

Single Droplet Digital Polymerase Chain Reaction for Comprehensive and Simultaneous Detection of Mutations in Hotspot Regions

Droplet digital polymerase chain reaction (ddPCR) is a highly sensitive quantitative polymerase chain reaction (PCR) method based on sample fractionation into thousands of nano-sized water-in-oil individual reactions. Recently, ddPCR has become one of the most accurate and sensitive tools for circulating tumor DNA (ctDNA) detection. One of the major limitations of the standard ddPCR technique is the restricted number of mutations that can be screened per reaction, as specific hydrolysis probes recognizing each possible allelic version are required. An alternative methodology, the drop-off ddPCR, increases throughput, since it requires only a single pair of probes to detect and quantify potentially all genetic alterations in the targeted region. Drop-off ddPCR displays comparable sensitivity to conventional ddPCR assays with the advantage of detecting a greater number of mutations in a single reaction. It is cost-effective, conserves precious sample material, and can also be used as a discovery tool when mutations are not known a priori.

Here, we present a protocol to accurately quantify multiple genetic alterations of a target region in a single reaction using drop-off ddPCR and a unique pair of hydrolysis probes.

Droplet digital polymerase chain reaction (ddPCR) is a highly sensitive quantitative polymerase chain reaction (PCR) method based on sample fractionation ...

Circulating MicroRNA Quantification Using DNA-binding Dye Chemistry and Droplet Digital PCR

Circulating (of cell-free) microRNAs (miRNAs) are released from cells into the blood stream. The amount of specific microRNAs in the circulation has been linked to a disease state and has the potential to be used as disease biomarker. A sensitive and accurate method for circulating microRNA quantification using a dye-based chemistry and droplet digital PCR technology has been recently developed. Specifically, using Locked Nucleic Acid (LNA)-based miRNA-specific primers with a green fluorescent DNA-binding dye in a compatible droplet digital PCR system it is possible to obtain the absolute quantification of specific miRNAs. Here, we describe how performing this technique to assess miRNA amount in biological fluids, such as plasma and serum, is both feasible and effective.

A sensitive and accurate method for cell-free microRNAs quantification using a dye-based chemistry and droplet digital PCR technology is described.

Circulating (of cell-free) microRNAs (miRNAs) are released from cells into the blood stream. The amount of specific microRNAs in the circulation has been ...

Bioengineering

High-Throughput Quantification of the Synthesis and Distribution of mtDNA

High-Throughput Image-Based Quantification of Mitochondrial DNA Synthesis and Distribution

The vast majority of cellular processes require a continuous supply of energy, the most common carrier of which is the ATP molecule. Eukaryotic cells produce most of their ATP in the mitochondria by oxidative phosphorylation. Mitochondria are unique organelles because they have their own genome that is replicated and passed on to the next generation of cells. In contrast to the nuclear genome, there are multiple copies of the mitochondrial genome in the cell. The detailed study of the mechanisms responsible for the replication, repair, and maintenance of the mitochondrial genome is essential for understanding the proper functioning of mitochondria and whole cells under both normal and disease conditions. Here, a method that allows the high-throughput quantification of the synthesis and distribution of mitochondrial DNA (mtDNA) in human cells cultured in vitro is presented. This approach is based on the immunofluorescence detection of actively synthesized DNA molecules labeled by 5-bromo-2'-deoxyuridine (BrdU) incorporation and the concurrent detection of all the mtDNA molecules with anti-DNA antibodies. Additionally, the mitochondria are visualized with specific dyes or antibodies. The culturing of cells in a multi-well format and the utilization of an automated fluorescence microscope make it easier to study the dynamics of mtDNA and the morphology of mitochondria under a variety of experimental conditions in a relatively short time.

Author Spotlight: High-Throughput Image-Based Quantification of Mitochondrial DNA Synthesis and Distribution  

A procedure for studying the dynamics of mitochondrial DNA (mtDNA) metabolism in cells using a multi-well plate format and automated immunofluorescence imaging to detect and quantify mtDNA synthesis and distribution is described. This can be further used to investigate the effects of various inhibitors, cellular stresses, and gene silencing on mtDNA metabolism.

The vast majority of cellular processes require a continuous supply of energy, the most common carrier of which is the ATP molecule. Eukaryotic cells ...

Biochemistry

Use of Bisection to Reduce Mitochondrial DNA in the Bovine Oocyte

Interspecies somatic cell nuclear transfer (iSCNT) may be used to rescue endangered species, but two distinct populations of mitochondrial DNA (mtDNA) exist within the reconstructed embryo: one within the recipient ooplasm and one within the donor somatic cell. This mitochondrial heteroplasmy can lead to developmental issues in the embryo and the fetus. Handmade cloning protocols include oocyte bisection, which can be used to decrease the mtDNA copy number, reducing the degree of mitochondrial heteroplasmy in a reconstructed embryo. Centrifugation of denuded, mature bovine oocytes produced a visible mitochondria-dense fraction at one pole of the oocyte. Oocytes&#39; zonae pellucidae were removed by exposure to a pronase solution. Bisection was performed using a microblade to remove the visible mitochondria fraction. qPCR was used to quantify the mtDNA present in DNA samples extracted from whole oocytes and bisected ooplasts, providing a comparison of mtDNA copy numbers before and after bisection. Copy numbers were calculated using cycle threshold values, a standard curve&#39;s regression line formula, and a ratio that included the respective sizes of mtDNA PCR products and genomic PCR products. One bovine oocyte had an average mtDNA copy number (&#177; standard deviation) of 137,904 &#177; 94,768 (n = 38). One mitochondria-depleted ooplast had an average mtDNA copy number of 8,442 &#177; 13,806 (n = 33). Average mtDNA copies present in a mitochondria-rich ooplast were 79,390 &#177; 58,526 mtDNA copies (n = 28). The differences between these calculated averages indicate that the centrifugation and subsequent bisection can significantly decrease the mtDNA copy numbers present in the mitochondria-depleted ooplast when compared to the original oocyte (P &#60; 0.0001, determined by one-way ANOVA). The reduction in mtDNA should decrease the degree of mitochondrial heteroplasmy in a reconstructed embryo, possibly fostering standard embryonic and fetal development. Supplementation with mitochondrial extract from the somatic donor cell may also be essential to achieve successful embryonic development.

Here, we present a protocol to significantly reduce the mitochondrial DNA copy numbers in a bovine oocyte (P &lt; 0.0001). This method utilizes centrifugation and bisection to substantially reduce oocyte mitochondria and may allow for an increased chance of development in the reconstructed interspecies somatic cell nuclear transfer embryos.

Interspecies somatic cell nuclear transfer (iSCNT) may be used to rescue endangered species, but two distinct populations of mitochondrial DNA (mtDNA) ...

Developmental Biology

Methylation Specific Multiplex Droplet PCR using Polymer Droplet Generator Device for Hematological Diagnostics

A multiplexed droplet PCR (mdPCR) workflow and detailed protocol for determining epigenetic-based white blood cell (WBC) differential count is described, along with a thermoplastic elastomer (TPE) microfluidic droplet generation device. Epigenetic markers are used for WBC&#160;subtyping which is of important prognostic value in different diseases. This is achieved through the quantification of DNA methylation patterns of specific CG-rich regions in the genome (CpG loci). In this paper, bisulfite-treated DNA from peripheral blood mononuclear cells (PBMCs) is encapsulated in droplets with mdPCR reagents including primers and hydrolysis fluorescent probes specific for CpG loci that correlate with WBC sub-populations. The multiplex approach allows for the interrogation of many CpG loci without the need for separate mdPCR reactions, enabling more accurate parametric determination of WBC sub-populations using epigenetic analysis of methylation sites. This precise quantification can be extended to different applications and highlights the benefits for clinical diagnosis and subsequent prognosis.

Epigenetic markers are used for white blood cell (WBC) subtyping through the quantification of DNA methylation patterns. This protocol presents a multiplex droplet polymerase chain reaction (mdPCR) method using a thermoplastic elastomer (TPE)-based microfluidic device for droplet generation allowing for precise and multiplex methylation-specific target quantification of WBC differential counts.

A multiplexed droplet PCR (mdPCR) workflow and detailed protocol for determining epigenetic-based white blood cell (WBC) differential count is described, ...

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays

Digital assays are powerful methods that enable detection of rare cells and counting of individual nucleic acid molecules. However, digital assays are still not routinely applied, due to the cost and specific equipment associated with commercially available methods. Here we present a simplified method for readout of digital droplet assays using a conventional real-time PCR instrument to measure bulk fluorescence of droplet-based digital assays.
We characterize the performance of the bulk readout assay using synthetic droplet mixtures and a droplet digital multiple displacement amplification (MDA) assay. Quantitative MDA particularly benefits from a digital reaction format, but our new method&#160;applies to any digital assay. For established digital assay protocols such as digital PCR, this method serves to speed up and simplify assay readout.
Our bulk readout methodology brings the advantages of partitioned assays without the need for specialized readout instrumentation. The principal limitations of the bulk readout methodology are reduced dynamic range compared with droplet-counting platforms and the need for a standard sample, although the requirements for this standard are less demanding than for a conventional real-time experiment. Quantitative whole genome amplification (WGA) is used to test for contaminants in WGA reactions and is the most sensitive way to detect the presence of DNA fragments with unknown sequences, giving the method great promise in diverse application areas including pharmaceutical quality control and astrobiology.

We describe an endpoint digital assay for quantifying nucleic acids with a simplified (analog) readout. We measure bulk fluorescence of droplet-based digital assays using a standard qPCR machine rather than specialized instrumentation and confirm our results by microscopy.

Digital assays are powerful methods that enable detection of rare cells and counting of individual nucleic acid molecules. However, digital assays are ...

Biology

Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing

Mutations in the mitochondrial genome (mtDNA) have been associated with maternally inherited genetic diseases. However, interest in mtDNA polymorphisms has increased in recent years due to the recently developed ability to produce models by mtDNA mutagenesis and a new appreciation of the association between mitochondrial genetic aberrations and common age-related diseases such as cancer, diabetes, and dementia. Pyrosequencing is a sequencing-by-synthesis technique that is widely employed across the mitochondrial field for routine genotyping experiments. Its relative affordability when compared to massive parallel sequencing methods and ease of implementation make it an invaluable technique in the field of mitochondrial genetics, allowing for the rapid quantification of heteroplasmy with increased flexibility. Despite the practicality of this method, its implementation as a means of mtDNA genotyping requires the observation of certain guidelines, specifically to avoid certain biases of biological or technical origin. This protocol outlines the necessary steps and precautions in designing and implementing pyrosequencing assays for use in the context of heteroplasmy measurement.

Pyrosequencing assays enable the robust and rapid genotyping of mitochondrial DNA single nucleotide polymorphisms in heteroplasmic cells or tissues.

Mutations in the mitochondrial genome (mtDNA) have been associated with maternally inherited genetic diseases. However, interest in mtDNA polymorphisms ...

Quantification of Circular RNAs Using Digital Droplet PCR

Digital droplet polymerase chain reaction (dd-PCR) is one of the most sensitive quantification methods; it fractionates the reaction into nearly 20,000 water-in-oil droplets, and the PCR occurs in the individual droplets. The dd-PCR has several advantages over conventional real-time qPCR, including increased accuracy in detecting low-abundance targets, omitting reference genes for quantification, eliminating technical replicates for samples, and showing high resilience to inhibitors in the samples. Recently, dd-PCR has become one of the most popular methods for accurately quantifying target DNA or RNA for gene expression analysis and diagnostics. Circular RNAs (circRNAs) are a large family of recently discovered covalently closed RNA molecules lacking 5' and 3' ends. They have been shown to regulate gene expression by acting as sponges for RNA-binding proteins and microRNAs. Furthermore, circRNAs are secreted into body fluids, and their resistance to exonucleases makes them serve as biomarkers for disease diagnosis. This article aims to show how to perform divergent primer design, RNA extraction, cDNA synthesis, and dd-PCR analysis to accurately quantify specific circular RNA (circRNA) levels in cells. In conclusion, we demonstrate the precise quantification of circRNAs using dd-PCR.

This protocol describes the detailed method of digital droplet PCR (dd-PCR) for precise quantification of circular RNA (circRNA) levels in cells using divergent primers.

Digital droplet polymerase chain reaction (dd-PCR) is one of the most sensitive quantification methods; it fractionates the reaction into nearly 20,000 ...

Duplex Digital PCR for Simultaneous Quantification of Dual Genetic Markers

To begin this procedure, first, prepare 100 micromole per liter stock concentrations for all primers in molecular-grade water and probes in TE pH 8 buffer, as described in the protocol text. Next, prepare a master mix by mixing appropriate amounts of digital PCR mix, forward and reverse primers, the fluorescent probe, and nuclease-free water. Pipette up and down at least 10 times to mix, while taking caution not to introduce air bubbles in the solution.
Since dPCR master mix is more viscous than conventional qPCR master mix, it&#39;s necessary to use the mixing by pipetting technique in order to create a homogeneous solution. This allows for accurate dPCR quantification downstream.
To make the assay mixture for droplet generation for running samples in duplicate, pipette 36 microliters of the master mix into a regular PCR plate. To each of the 36-microliter master mixes, mix in 12 microliters of DNA template, leaving the corresponding replicate wells empty on the plate. Include positive controls to ensure the assay is running properly. Include No Template Controls or NTCs to ensure there is no contamination within the plate, and to set the fluorescent baseline later for data analysis.
Prior to setting up the droplet generator, mix the assay mixtures by using a multichannel pipette to pipette the mixtures up and down approximately 15 times. Ensure that the pipette tip stays within the liquid to avoid making excess bubbles within the mixture.
Next, insert cartridge one, containing eight wells, into a white cartridge holder and click the cartridge holder shut. Cartridge one is now firmly in place, and cannot be dislodged from the holder while generating droplets.
Using a multichannel pipette, gently transfer 20 microliters of the assay mixture into the middle position of the cartridge marked &#39;Sample&#39; without introducing air bubbles. Pipette in 70 microliters of droplet generation oil to the left side of the cartridge marked &#39;Oil.&#39;
Cover the cartridge with a gasket, making sure the gasket is flat and held evenly by the four ticks toward the edge of the cartridge. Press the green-lit button on the droplet generator to open the door and place the cartridge. Press the button again to close the generator. Once the door closes, the green button is dimmed and the door cannot be reopened.
Droplet generation will begin immediately and continue for approximately 1 minute.
While the droplet generation is in progress, place cartridge two in a second white cartridge holder, and prepare it in the same manner as for cartridge one. When the droplet generation is complete, the dimly-lit button will turn green.
Open the droplet generator door. Remove the white cartridge holder containing cartridge one and set it aside. Place cartridge two into the droplet generator.
Remove the gasket from cartridge one and discard. Do not unclick the white cartridge holder, as the action may break the newly-generated droplets.
Using a multichannel pipette set to 40 microliters, insert the tips into the third column of the cartridge marked droplets at a 45-degree angle, and slowly pipette up all the droplets. Transfer them to the final PCR plate by putting the pipette tip against the well wall approximately halfway down and expelling the droplet slowly.
In the same way, when the droplet generation for cartridge two is complete, remove the gasket from cartridge two, and transfer the generated droplets to the final PCR plate. Place a pierceable foil cover on top of the plate and place it on a plate sealer. Set the sealer to 180 degrees Celsius. Press &#34;Play&#34; on the sealer and seal for 10 seconds.
To begin this procedure, place the sealed final PCR plate in the thermal cycler. Use a thermal cycler that is compatible with the final PCR plate, and with a temperature ramping speed of 2 degrees Celsius per second.
Run the following thermal program: 10 minutes at 95 degrees Celsius followed by 40 cycles of 30 seconds at 94 degrees Celsius and 60 seconds at 60 degrees Celsius followed by a 10-minute hold at 98 degrees Celsius. Upon completion of cycling, transfer the plate to a droplet reader for automatic measurement of fluorescence in each droplet in each well.
Ensure the droplets are at room temperature before proceeding with droplet reading. Start by opening the accompanying software to set up the droplet reading. In the default &#34;Setup&#34; menu containing a schematic of an empty 96-well plate, double-click on well A1 to open the menu containing three sections -- &#34;Sample,&#34; &#34;Assay 1,&#34; and &#34;Assay 2.&#34;
In the sample section, type the sample ID into the box labeled &#34;Name&#34; and check the box to the right marked &#34;Apply.&#34; Next, click the dropdown menu labeled &#34;Experiment.&#34; Choose &#34;RED&#34; for Rare Event Detection and click &#39;Enter.&#39;
Move to the section denoted as &#34;A1.&#34; In the &#34;Name&#34; section, fill out the assay and click &#39;Enter.&#39; In the box below labeled &#34;Type,&#34; click the dropdown menu, choose &#34;Channel 1 Unknown,&#34; and click &#39;Enter.&#39;
Move to the section denoted as &#34;A2.&#34; In the &#34;Name&#34; section, fill out the assay and click &#39;Enter.&#39; In the box below labeled &#34;Type,&#34; click the dropdown menu, choose &#34;Channel 2 Unknown,&#34; and click &#39;Enter.&#39;
All the information from the previous steps is now present in well A1.
Name all subsequent wells containing droplets. To save total setup time, click &#39;Shift&#39; or &#39;Control&#39; to choose multiple wells simultaneously. When the digital depiction of the plate mirrors the physical plate, press &#34;OK&#34; at the bottom right of the menu. In the new menu that appears at the top of the plate schematic, under the &#34;Template&#34; section, choose &#34;Save As&#34; and name and save the plate.
To the left of the screen, click &#34;Run&#34; and select the appropriate Dye Set in the pop-out &#34;Run Options&#34; window. Data collection will initiate and is displayed in real-time time in the software.