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Reagents
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蛋白质印迹试剂
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Single-Cell Multiomics Reagents
- 附件
- BD® AbSeq Assay
- BD Rhapsody™ 附件试剂盒
- BD® Single-Cell Multiplexing Kit
- BD Rhapsody™ TCR/BCR Next Multiomic Assays
- BD Rhapsody™ Targeted mRNA Kits
- BD Rhapsody™ Whole Transcriptome Analysis (WTA) Amplification Kit
- BD Rhapsody™ TCR/BCR Profiling Assays
- BD® OMICS-Guard Sample Preservation Buffer
- BD Rhapsody™ ATAC-Seq Assays
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Functional Assays
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显微成像试剂
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Cell Preparation and Separation Reagents
- Dehydrated Culture Media
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- 附件
- BD® AbSeq Assay
- BD Rhapsody™ 附件试剂盒
- BD® Single-Cell Multiplexing Kit
- BD Rhapsody™ TCR/BCR Next Multiomic Assays
- BD Rhapsody™ Targeted mRNA Kits
- BD Rhapsody™ Whole Transcriptome Analysis (WTA) Amplification Kit
- BD Rhapsody™ TCR/BCR Profiling Assays
- BD® OMICS-Guard Sample Preservation Buffer
- BD Rhapsody™ ATAC-Seq Assays
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Redefine CITE-seq
The Intracellular CITE-seq Assay using BD® AbSeq Antibody-Oligos:
- Enables simultaneous RNA, surface protein and intracellular protein detection
- Supports high-plex proteomics profiling (~100 protein markers) at the single-cell level
- Allows a safe stopping point during the workflow without compromising assay sensitivity
- Works with the BD® Single-Cell Multiplexing Kit to enable sample multiplexing
- Drives deeper understanding of cellular functions such as signal transduction dynamics and transcriptional regulation
Get more information from the Intracellular CITE-seq Assay using BD® AbSeq Antibody-Oligos brochure.
List of Available Intracellular BD® AbSeq Ab-Oligo Specificities
Specificity | Clone |
Caspase-3 | C92-605 |
PARP (Cleaved) | F21-852 |
H2AX (pS139) | N1-431 |
T-bet | O4-46 |
Granzyme B | GB11 |
Helios | 22F6 |
BCL-6 | K112-91 |
GATA3 | L50-823 |
Ki-67 | B56 |
Stat6 (pY641) | 18/P-Stat6 |
p38 MAPK (pT180/pY182) | 36/p38 (pT180/pY182) |
Chromogranin A | S21-537 |
Sox2 | O30-678 |
Sox17 | P7-969 |
Applications
Intracellular BD® AbSeq Antibody-Oligos can be used to characterize a heterogeneous subset of T follicular helper (TFH) cells in human tonsil
A combination of intracellular CITE-seq, surface CITE-seq and scRNA-seq was used to deepen our understanding of the differentiation states and subsets of cells present at low abundance, such as TFH cells.
We characterized the heterogeneous subsets of TFH and circulating TFH (cTFH) cells using a combination of intracellular CITE-seq, surface CITE-seq and whole transcriptome single-cell RNA sequencing (scRNA-seq) analysis. Germinal center and cTFH cells were enriched by sorting memory CD4+, CXCR5+, PD-1+ from a tonsil (n = 1) and memory CD4+ CXCR5+ cells from a matched blood sample and a healthy blood donor (n = 2). We examined the expression of Bcl-6 and other transcription factors, using protein and RNA expression data, across pre-TFH (an early development stage in the germinal center), TFH and cTFH cells.
For Research Use Only. Not for use in diagnostic or therapeutic procedures
23-22990-00
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