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Anti-HLA-A*02 Recombinant Antibody (BB7.2) (HM833053)

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Overview
Catalog No.HM833053
Description
Anti-HLA-A*02 Recombinant Antibody (BB7.2) (HM833053) is a mouse monoclonal antibody detecting HLA-A*02 in IP, FCM.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
ApplicationsIP, FCM
Host speciesMouse
ClonalityMonoclonal
IsotypeIgG2b, kappa
Clone IDBB7.2
Target HLA class I histocompatibility antigen, A alpha chain, HLA-A, HLAA, Human leukocyte antigen A
Endotoxin level < 10 EU/mg as determined by LAL method.
Purity >95% as determined by SDS-PAGE.
Purification Protein A/G purified from cell culture supernatant.
Accession P04439
Form Liquid
Storage buffer 0.01M PBS pH 7.4.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

HLA class I histocompatibility antigen, A alpha chain (HLA-A2) is a ~40 kDa protein. Antigen-presenting major histocompatibility complex class I (MHCI) molecule. In complex with B2M/beta 2 microglobulin displays primarily viral and tumor-derived peptides on antigen-presenting cells for recognition by alpha-beta T cell receptor (TCR) on HLA-A-restricted CD8-positive T cells, guiding antigen-specific T cell immune response to eliminate infected or transformed cells. May also present self-peptides derived from the signal sequence of secreted or membrane proteins, although T cells specific for these peptides are usually inactivated to prevent autoreactivity. Both the peptide and the MHC molecule are recognized by TCR, the peptide is responsible for the fine specificity of antigen recognition and MHC residues account for the MHC restriction of T cells. Typically presents intracellular peptide antigens of 8 to 13 amino acids that arise from cytosolic proteolysis via IFNG-induced immunoproteasome or via endopeptidase IDE/insulin-degrading enzyme.

1. Fukada, K. et al. (1999) AIDS (London, England) 13, 1413-4. PMID: 10449296
2. Nagata, Y. et al. (2002) Proceedings of the National Academy of Sciences of the United States of America 99, 10629-34. PMID: 12138174
3. Kuzushima, K. et al. (2003) Blood 101, 1460-8. PMID: 12393434
4. Traversari, C. et al. (1992) The Journal of experimental medicine 176, 1453-7. PMID: 1402688
5. Satoh, M. et al. (2005) Vaccine 23, 3783-90. PMID: 15893615
6. Asemissen, AM. et al. (2006) Clinical cancer research : an official journal of the American Association for Cancer Research 12, 7476-82. PMID: 17189421
7. Hadrup, SR. et al. (2009) Nature methods 6, 520-6. PMID: 19543285
8. Matthews, PC. et al. (2011) Journal of immunology (Baltimore, Md. : 1950) 186, 5675-86. PMID: 21498667
9. Shimizu, A. et al. (2013) Scientific reports 3, 3097. PMID: 24192765
10. Quiñones-Parra, S. et al. (2014) Proceedings of the National Academy of Sciences of the United States of America 111, 1049-54. PMID: 24395804
Note For research use only.
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Formula
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