R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
Phospho-CD28 (Tyr191) (E5B9Z) Rabbit mAb #16399
Filter:
- WB
- IP
Supporting Data
REACTIVITY | H M |
SENSITIVITY | Endogenous |
MW (kDa) | 40 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
- M-Mouse
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:200 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
Phospho-CD28 (Tyr191) (E5B9Z) Rabbit mAb recognizes endogenous levels of CD28 protein only when phosphorylated at Tyr191. This antibody shows cross-reactivity with phosphorylated EGFR, ERBB2, and CSF1R, and detects a 70-80 kDa band of unknown origin in some treated cell lines.
Species Reactivity:
Human, Mouse
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Tyr191 of human CD28 protein.
Background
CD28 is a transmembrane glycoprotein expressed by T cells as well as some other hematopoietic cells (1, 2). T cell activation requires T cell receptor (TCR) recognition of antigen presented in the context of MHC molecules. CD28 acts as a T cell costimulatory receptor, and interaction of CD28 with its ligands CD80 or CD86 provides the second signal required for naïve T cell activation (3-5). Activation of naïve T cells in the absence of CD28 stimulation can result in a state of T cell anergy, or unresponsiveness (3). CD28 signals through cytoplasmic phospho-tyrosine motifs that bind several SH2 or SH3 domain-containing proteins involved in T cell activation (2). Recently, CD28 was demonstrated to be a preferred target of PD-1-mediated dephosphorylation. Consistently, CD28 expression was required for T cell proliferation following PD-1 blockade and CD28 stimulation was required for effective anti-PD-1 cancer immunotherapy in mice (6, 7). Several CD28 isoforms are produced by alternative splicing (8).
- Aruffo, A. and Seed, B. (1987) Proc Natl Acad Sci U S A 84, 8573-7.
- Esensten, J.H. et al. (2016) Immunity 44, 973-88.
- Harding, F.A. et al. (1992) Nature 356, 607-9.
- Azuma, M. et al. (1993) Nature 366, 76-9.
- Linsley, P.S. et al. (1990) Proc Natl Acad Sci U S A 87, 5031-5.
- Hui, E. et al. (2017) Science 355, 1428-1433.
- Kamphorst, A.O. et al. (2017) Science 355, 1423-1427.
- Magistrelli, G. et al. (1999) Biochem Biophys Res Commun 259, 34-7.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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