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SRX24368352: GSM8230007: Sort-purified (CD8/CD45.1) TCR OT1 CD8 T cells from B16-OVA-GP61 tumors (with TCR SMARTA CD4 T cells) replicate#2 [ATAC]; Mus musculus; ATAC-seq
1 ILLUMINA (Illumina HiSeq 2500) run: 138.6M spots, 13.9G bases, 5.3Gb downloads

External Id: GSM8230007_r1
Submitted by: Immunology, Memorial Sloan Kettering Cancer Center
Study: The role of CD4 T cells in tumor-specific CD8 T cell reprogramming [ATAC-Seq]
show Abstracthide Abstract
ATAC-seq analysis of tumor-specific CD8 T cells from tumors with and without tumor-specific CD4 T cells Overall design: T cells were sorted by flow cytometry and ATAC-seq was performed.
Sample: Sort-purified (CD8/CD45.1) TCR OT1 CD8 T cells from B16-OVA-GP61 tumors (with TCR SMARTA CD4 T cells) replicate#2 [ATAC]
SAMN41082924 • SRS21125188 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM8230007
Instrument: Illumina HiSeq 2500
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: CD8 T cells were FACS-sorted into FCS containing tubes and after sort 10% DMSO were added, mixed and stored at -80°C until all samples were collected. Profiling of Chromatin was performed by ATAC-seq. Cells were thawed and washed in cold PBS and lysed. After cell lysis, transposition happened at 42ºC for 45 min. After purification of the DNA with the MinElute PCR purification kit (Qiagen), material was amplified for 5 cycles. Additional PCR cycles were evaluated by real time PCR. Final product was cleaned by Ampure Beads at a 1.5x ratio. Libraries were sequenced on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 47x106 paired reads were generated per sample.
Runs: 1 run, 138.6M spots, 13.9G bases, 5.3Gb
Run# of Spots# of BasesSizePublished
SRR28804600138,622,50213.9G5.3Gb2024-05-19

ID:
32683171

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