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QPCTL deletion results in a rewiring of the tumor microenvironment [scRNA-seq]. QPCTL deletion results in a rewiring of the tumor microenvironment [scRNA-seq]

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NIAID Data Ecosystem2026-03-12 收录
下载链接:
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA746810
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资源简介:
single cell RNA sequencing performed on the FACS sorted tumor microenvironment of (QPCTL-proficient and -deficient) B16F10 tumors Overall design: C57/Bl6JR mice that were QPCTL-WT or QPCTL-KO were innoculated with either QPCTL-proficient or deficient B16F10 tumor cells, respectively (n=3 each). After 14 days tumors were harvested, single cell suspensions were made and live cells were isolated by FACS, after which cells were processed for scRNA-seq (10X Chromium 3' kit), and sequenced on Illumina NextSeq

本研究针对经荧光激活细胞分选(Fluorescence-Activated Cell Sorting, FACS)分离的QPCTL功能正常型与功能缺陷型(QPCTL-proficient and -deficient)B16F10肿瘤的肿瘤微环境,开展单细胞RNA测序(single cell RNA sequencing, scRNA-seq)。实验设计:将QPCTL野生型(QPCTL-WT)与QPCTL基因敲除型(QPCTL-KO)的C57/Bl6JR小鼠分别接种对应基因型的QPCTL功能正常型及功能缺陷型B16F10肿瘤细胞,每组各3个生物学重复。接种14天后获取肿瘤组织,制备单细胞悬液并通过FACS分离活细胞,随后采用10X Chromium 3'试剂盒处理细胞以进行scRNA-seq,并在Illumina NextSeq测序平台完成测序。
创建时间:
2021-07-15
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