SKU: 85670802049

Alexa Fluor® 488 Mouse Anti-Human CD28 Antibody (15E8)

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Description

Alexa Fluor® 488 Mouse Anti-Human CD28 Antibody (15E8)Product Specification Host Mouse Antigen CD28 Synonyms TP44 Immunogen N A Location Membrane Accession P10747 Clone Number 15E8 Antibody Type Recombinant mAb Isotype IgG1,k Application FCM Reactivity Hu Purification Protein G Concentration 0. 2mg ml Conjugation Alexa Fluor 488 Physical Appearance Liquid Storage Buffer PBS, 0. 1% BSA, 0. 01% Proclin 300 Stability & Storage 12 months from date of receipt reconstitution, 2 to 8 C as supplied. Dilution

Product Specification


Host Mouse
Antigen CD28
Synonyms TP44
Immunogen N/A
Location Membrane
Accession P10747
Clone Number 15E8
Antibody Type Recombinant mAb
Isotype IgG1,k
Application FCM
Reactivity Hu
Purification Protein G
Concentration 0.2mg/ml
Conjugation Alexa Fluor® 488
Physical Appearance Liquid
Storage Buffer

PBS, 0.1% BSA, 0.01% Proclin 300

Stability & Storage 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.

Dilution


application dilution species
FCM 5μl per million cells in 100μl volume

Background

CD28 (Cluster of Differentiation 28) is one of the proteins expressed on T cells that provide co-stimulatory signals required for T cell activation and survival. T cell stimulation through CD28 in addition to the T-cell receptor (TCR) can provide a potent signal for the production of various interleukins (IL-6 in particular). CD28 is the receptor for CD80 (B7.1) and CD86 (B7.2) proteins. When activated by Toll-like receptor ligands, the CD80 expression is upregulated in antigen-presenting cells (APCs). The CD86 expression on antigen-presenting cells is constitutive (expression is independent of environmental factors). It is generally reported, that CD28 is expressed on 50% of CD8+ T cells and more than 80% CD4+ T cells in human, but during the course of activation some T cells lose this molecule. In general, CD28 is a primary costimulatory molecule for T cell activation.

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SKU: 85670802049

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Reviewed in the United States on February 28, 2026
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Reviewed in the United States on August 20, 2025
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