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Anti cd39

Manufactured by BD
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Sourced in United States

Anti-CD39 is a monoclonal antibody used for the detection and quantification of CD39, a cell surface molecule expressed on various cell types. It is a useful tool for research applications involving the study of CD39 and its role in immunological and physiological processes.

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Lab products found in correlation

Anti cd45ra, by BD (1 mentions) Foxp3 staining kit, by Thermo Fisher Scientific (1 mentions) Anti cd44, by BD (1 mentions) Anti cd127, by BD (1 mentions) Anti ccr7, by BD (1 mentions) Anti cxcr3, by BD (1 mentions) Anti cd62l, by BD (1 mentions) Lsrfortessa, by BD (1 mentions) Anti cd3, by BD (1 mentions) Anti cd4, by BD (1 mentions) Anti cd27 pe, by BD (1 mentions) Anti cd73, by BD (1 mentions) Facsaria 2, by BD (1 mentions)

Spelling variants of this product

FITC-conjugated anti-human CD39 (2 citations) APC conjugated anti-CD39 (2 citations)

2 protocols using anti cd39

1

Multiparametric T cell immunophenotyping

Cited 1 time
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Single cell suspensions of T cells were stained as described [17 (link)] at 4°C with fluorochrome-labeled anti-CD3, anti-CD4, anti-CD25, anti-CD27-PE, anti-CD39, anti-CD44, anti-CD45RA, anti-CD62L, anti-CD127, anti-CXCR3, anti-CCR7 (BD PharMingen, Franklin Lakes, NJ, or BioLegend, San Diego, CA). Intracellular Foxp3, cytotoxic T lymphocyte Ag-4 (CTLA-4), Helios, T-bet, IL-2, IL-17 and IFN-γ were stained using an eBioscience Foxp3 Staining kit, according to the manufacturer’s instructions. Data were acquired on a LSR II or LSR Fortessa (BD Bioscience) and analyzed with FlowJo software (Tree Star, Ashland, OR, USA).
Guo H., Zhang H., Lu L., Ezzelarab M.B, & Thomson A.W. (2015). Generation, cryopreservation, function and in vivo persistence of ex-vivo expanded cynomolgus monkey regulatory T cells. Cellular immunology, 295(1), 19-28.
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2

Immunophenotyping of CD45+, CD39+, and CD73+ cells

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SVCs were stained with anti-CD45PAN (BioLegend, San Diego, CA, USA), anti-CD39 (BD PharMingen, San Diego, CA, USA), and anti-CD73 (BD PharMingen) antibodies. Isotype-matched mAb were used as controls. Data were acquired by use of a FACSAria II (BD Biosciences, San Jose, CA, USA) and analyzed with FlowJo software. Statistical analyses were based on at least 100,000 events gated on the population of interest.
Pandolfi J., Ferraro A., Lerner M., Serrano J.R., Dueck A., Fainboim L, & Arruvito L. (2015). Purinergic signaling modulates human visceral adipose inflammatory responses: implications in metabolically unhealthy obesity. Journal of leukocyte biology, 97(5).
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