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Evolution of antigen-specific follicular helper T cell transcriptional progams across effector function and through to memory. Evolution of antigen-specific follicular helper T cell transcriptional progams across effector function and through to memory

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NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA788946
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We utilized single cell-indexed custom RNA-sequencing to interogate the transcriptomes of TFH cells at Day 7, Day 14, and Day 28 following NP-PCC immunization Overall design: T cells were isolated from draining lymph nodes of B10.Br mice following base of tail immunization with NP-PCC in MPL at Day 7, Day 14, and D28. Phenotypically defined T cell subsets sorted as: naïve CD4 T cells (CD4+, CD8- CD62L+, CD44-), Effector T helper cells (CD4+, CD8- CD44+ CD62L-, CXCR5-), T follicular cells (CD4+, CD8-, CD44+. CD62L-, CXCR5+). Cells were sorted into 384 well plates for library preparation. cDNA was amplied using a nested set of ~500 gene specific targeted primers.
创建时间:
2021-12-14
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