10X Genomics - 3' Single Cell Gene Expression analysis

The 3' single cell gene expression analysis workflow is a 3'-based workflow for analysing gene expression in individual cells. Individual cells are packed into nanoliter-sized water-in-oil droplets using the undefinedChromium Controller together with a gel bead containing a mixture of different barcodes. In this small reaction volume of about 1 nl, the cell is lysed and the mRNA molecules are barcoded via their polyA tail and transcribed into cDNA. Subsequently, the resulting emulsion is chemically broken and the cDNA is amplified in a sequence-independent manner. This amplified cDNA then serves as input for an Illumina-compatible library preparation. After sequencing, the sequences can then be bioinformatically assigned to the individual cells or transcripts on the basis of the attached barcodes.

A maximum of 8 samples can be processed in parallel on a single chip of the Chromium controller. For each sample, between 500 and 10,000 cells can be analysed. Approximately 50% of the cells used as input are actually analysed. Meaning that If 10,000 cells are to be analysed for a sample, 20,000 cells are needed as starting material.

Sample Requirements

As input material, a single cell suspension is required. This suspension has to meet two key criteria in order to deliver high-quality data.

On the one hand only truly single cells may be present in the suspension. If cell aggregates are present in the suspension, they have to be removed. On the other hand, the cells should have the highest possible vitality. The suspension should not contain more than about 20% of dead cells. An excessive amount of dead cells leads to a high background signal. If your samples does contain a higher proportion of dead cells it may be necessary to remove the dead cells.

After receiving the samples in our laboratory, a quality control is routinely performed determining both cell count and vitality of your sample.

Since for this type of analysis the input material is cell material, please clarify in advance with us whether your material may be processed in our laboratory!

  • Cell vitality: > 70%
  • Min. Concentration: 500 Cells/ul
  • Max. Concentration :1500 Cell/ul
  • Min. Volume: 70 ul (Allows reloading in case of clog)
  • recommended Buffer: PBS/0,5% BSA (no Mg++, EDTA)

Head of GTL

Prof. Dr. Karl Köhrer

Biologisch-Medizinisches Forschungszentrum (BMFZ) Heinrich-Heine-Universität Düsseldorf Universitätsstr. 1 40225 Düsseldorf
Phone +49 211 81-13165
Fax +49 211 81-11922
Responsible for the content: E-MailRedaktionsteam BMFZ