High-throughput single-cell transcriptome sequencing method and kit
A transcriptome sequencing and single-cell technology, applied in the field of single-cell sequencing, can solve the problems of inability to carry out large-scale research work, difficult detailed analysis of different cell subpopulations, constrained throughput, cost, etc., to reduce mutual contamination of microbeads , Convenient single-cell sequencing, and low-cost effects
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[0058] 1. Prepare reagents
[0059] (1) Cell resuspension
[0060] Prepare 5 mL of PBS-BSA with a final concentration of 0.01% BSA; wash the H1975 cell line with PBS-BSA, and resuspend the cells in PBS-BSA for later use.
[0061] (2) Cleavage and reverse transcription reaction reagent preparation
[0062] 1mL of lysis and reverse transcription reaction reagents include: 10% Triton-X 10μL, 0.1M DTT 125μL, RnaseOUT 75μL, 10Mm each dNTPs 50μL, 5×RT buffer400μL, Super Script II ReverseTranscriptase 75μL, Template Switch Oligo 20μL, Rnase-free H 2 O 265 μL.
[0063] Wherein, Template Switch Oligo is the sequence shown in SEQ ID NO.5,
[0064] SEQ ID NO.5: 5'-AAGCAGTGGTATCAACGCAGAGTGAATGGG-3'
[0065] In Template Switch Oligo, the penultimate 2nd and 3rd bases are modified with riboguanosine, and the last base is modified with LNA.
[0066] (3) Microbead resuspension
[0067] In this example, the microbeads have primer sequences with poly(T) random sequences, which can capture...
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