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AB316357

Anti-HLA-ABC Antibody [Bu8]

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Mouse Monoclonal HLA A antibody. Suitable for Flow Cyt, ICC/IF and reacts with Human samples. Immunogen corresponding to Native Cell within Human HLA-A.

View Alternative Names

HLAA, HLA-A, Human leukocyte antigen A

2 Images
Immunocytochemistry/ Immunofluorescence - Anti-HLA-ABC Antibody [Bu8] (AB316357)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-HLA-ABC Antibody [Bu8] (AB316357)

Immunofluorescence analysis of paraformaldehyde fixed Daudi (Human Burkitt's lymphoma cell line) cells. Primary incubation 1hr (1 : 50-1 : 100 dilution) followed by Alexa Fluor® 488 secondary antibody (1 : 1000 dilution), showing membrane staining. The nuclear stain is DAPI (blue). Isotype control : Anti-Fluorescein followed by Alexa Fluor® 488 secondary antibody.

Flow Cytometry - Anti-HLA-ABC Antibody [Bu8] (AB316357)
  • Flow Cyt

Supplier Data

Flow Cytometry - Anti-HLA-ABC Antibody [Bu8] (AB316357)

Blue line : Flow cytometric analysis of paraformaldehyde fixed Daudi (Human Burkitt's lymphoma cell line) cells. Primary incubation 1hr (1 : 50-1 : 100 dilution) followed by Alexa Fluor 488 ® conjugated goat Anti-mouse IgG (1 : 1000 dilution). Black line : Anti-Fluorescein Isotype control.

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

Bu8

Isotype

IgG1

Carrier free

No

Reacts with

Human

Applications

Flow Cyt, ICC/IF

applications

Immunogen

Native Cell within Human HLA-A.

P04439

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "FlowCyt" : {"fullname" : "Flow Cytometry", "shortname":"Flow Cyt"}, "ICCIF" : {"fullname" : "Immunocytochemistry/ Immunofluorescence", "shortname":"ICC/IF"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "FlowCyt-species-checked": "testedAndGuaranteed", "FlowCyt-species-dilution-info": "1/50 - 1/100", "FlowCyt-species-notes": "<p></p>", "ICCIF-species-checked": "testedAndGuaranteed", "ICCIF-species-dilution-info": "1/50 - 1/100", "ICCIF-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Storage buffer
Preservative: 0.1% Sodium azide Constituents: 99% PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1 month
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

HLA-A HLA-C and HLA-B are molecules from the human leukocyte antigen (HLA) class I family. These proteins help present peptide antigens to T cells and function in immune surveillance. Alternate names for these targets include MHC class I where MHC stands for Major Histocompatibility Complex. The molecular mass of the HLA class I molecule is approximately 45 kDa. These proteins have expression across almost all nucleated cells. A heavy chain and a light chain β2-microglobulin form these molecules and each plays a role in antigen presentation.
Biological function summary

These proteins play an important role in immune response modulation by presenting peptide fragments on the cell surface for recognition by CD8+ cytotoxic T cells. They operate as part of the HLA class I-peptide complex which informs the immune system about the health status of cells. Healthy cells present self-peptides while infected or cancerous cells display foreign or abnormal peptides. The signaling from HLA class I to T cells can either activate or inhibit immune responses depending on the context of the peptides presented. This ensures a targeted immune response which is important for maintaining health.

Pathways

HLA-A HLA-C and HLA-B are central to the antigen processing and presentation pathway as well as the immune checkpoint pathway. These proteins interact with various components involved in these pathways such as transporter associated with antigen processing (TAP) and Protein Disulfide Isomerase (PDI) which help in peptide translocation and loading onto MHC class I molecules. The interactions within these pathways help control the immune system's ability to distinguish between self and non-self-antigens ensuring precise immune regulation.

The expression or malfunction of HLA-A HLA-C and HLA-B links tightly to autoimmune diseases and transplant rejection. Altered HLA expression can dysregulate immune responses leading to diseases like rheumatoid arthritis. Additionally variations in these antigens impact how the immune system recognizes and attacks transplanted organs potentially causing rejection. These HLA molecules also work in connection with other proteins like cytokines impacting their role and the immune response in disease contexts.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

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 (PubMed : 10449296, PubMed : 12138174, PubMed : 12393434, PubMed : 1402688, PubMed : 15893615, PubMed : 17189421, PubMed : 19543285, PubMed : 21498667, PubMed : 24192765, PubMed : 24395804, PubMed : 2456340, PubMed : 2784196, PubMed : 28250417, PubMed : 7504010, PubMed : 7694806, PubMed : 9862734). 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 (PubMed : 25880248, PubMed : 7506728, PubMed : 7679507). 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 (PubMed : 12796775, PubMed : 18275829, PubMed : 19542454, PubMed : 28250417). 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 (PubMed : 17079320, PubMed : 17189421, PubMed : 20364150, PubMed : 26929325, PubMed : 27049119). Can bind different peptides containing allele-specific binding motifs, which are mainly defined by anchor residues at position 2 and 9 (PubMed : 7504010, PubMed : 9862734).. Allele A*01 : 01 : Presents a restricted peptide repertoire including viral epitopes derived from IAV NP/nucleoprotein (CTELKLSDY), IAV PB1/polymerase basic protein 1 (VSDGGPNLY), HAdV-11 capsid L3/hexon protein (LTDLGQNLLY), SARS-CoV-2 3a/ORF3a (FTSDYYQLY) as well as tumor peptide antigens including MAGE1 (EADPTGHSY), MAGEA3 (EVDPIGHLY) and WT1 (TSEKRPFMCAY), all having in common a canonical motif with a negatively charged Asp or Glu residue at position 3 and a Tyr anchor residue at the C-terminus (PubMed : 1402688, PubMed : 17189421, PubMed : 19177349, PubMed : 20364150, PubMed : 24395804, PubMed : 25880248, PubMed : 26758806, PubMed : 30530481, PubMed : 32887977, PubMed : 7504010). A number of HLA-A*01 : 01-restricted peptides carry a post-translational modification with oxidation and N-terminal acetylation being the most frequent (PubMed : 25880248). Fails to present highly immunogenic peptides from the EBV latent antigens (PubMed : 18779413).. Allele A*02 : 01 : A major allele in human populations, presents immunodominant viral epitopes derived from IAV M/matrix protein 1 (GILGFVFTL), HIV-1 env (TLTSCNTSV), HIV-1 gag-pol (ILKEPVHGV), HTLV-1 Tax (LLFGYPVYV), HBV C/core antigen (FLPSDFFPS), HCMV UL83/pp65 (NLVPMVATV) as well as tumor peptide antigens including MAGEA4 (GVYDGREHTV), WT1 (RMFPNAPYL) and CTAG1A/NY-ESO-1 (SLLMWITQC), all having in common hydrophobic amino acids at position 2 and at the C-terminal anchors.. Allele A*03 : 01 : Presents viral epitopes derived from IAV NP (ILRGSVAHK), HIV-1 nef (QVPLRPMTYK), HIV-1 gag-pol (AIFQSSMTK), SARS-CoV-2 N/nucleoprotein (KTFPPTEPK) as well as tumor peptide antigens including PMEL (LIYRRRLMK), NODAL (HAYIQSLLK), TRP-2 (RMYNMVPFF), all having in common hydrophobic amino acids at position 2 and Lys or Arg anchor residues at the C-terminus (PubMed : 19543285, PubMed : 21943705, PubMed : 2456340, PubMed : 32887977, PubMed : 7504010, PubMed : 7679507, PubMed : 9862734). May also display spliced peptides resulting from the ligation of two separate proteasomal cleavage products that are not contiguous in the parental protein (PubMed : 27049119).. Allele A*11 : 01 : Presents several immunodominant epitopes derived from HIV-1 gag-pol and HHV-4 EBNA4, containing the peptide motif with Val, Ile, Thr, Leu, Tyr or Phe at position 2 and Lys anchor residue at the C-terminus. Important in the control of HIV-1, EBV and HBV infections (PubMed : 10449296). Presents an immunodominant epitope derived from SARS-CoV-2 N/nucleoprotein (KTFPPTEPK) (PubMed : 32887977).. Allele A*23 : 01 : Interacts with natural killer (NK) cell receptor KIR3DL1 and may contribute to functional maturation of NK cells and self-nonself discrimination during innate immune response.. Allele A*24 : 02 : Presents viral epitopes derived from HIV-1 nef (RYPLTFGWCF), EBV lytic- and latent-cycle antigens BRLF1 (TYPVLEEMF), BMLF1 (DYNFVKQLF) and LMP2 (IYVLVMLVL), SARS-CoV nucleocapsid/N (QFKDNVILL), as well as tumor peptide antigens including PRAME (LYVDSLFFL), all sharing a common signature motif, namely an aromatic residue Tyr or Phe at position 2 and a nonhydrophobic anchor residue Phe, Leu or Iso at the C-terminus (PubMed : 12393434, PubMed : 20844028, PubMed : 24192765, PubMed : 9047241). Interacts with natural killer (NK) cell receptor KIR3DL1 and may contribute to functional maturation of NK cells and self-nonself discrimination during innate immune response (PubMed : 17182537, PubMed : 18502829).. Allele A*26 : 01 : Presents several epitopes derived from HIV-1 gag-pol (EVIPMFSAL, ETKLGKAGY) and env (LVSDGGPNLY), carrying as anchor residues preferentially Glu at position 1, Val or Thr at position 2 and Tyr at the C-terminus.. Allele A*29 : 02 : Presents peptides having a common motif, namely a Glu residue at position 2 and Tyr or Leu anchor residues at the C-terminus.. Allele A*32 : 01 : Interacts with natural killer (NK) cell receptor KIR3DL1 and may contribute to functional maturation of NK cells and self-nonself discrimination during innate immune response.. Allele A*68 : 01 : Presents viral epitopes derived from IAV NP (KTGGPIYKR) and HIV-1 tat (ITKGLGISYGR), having a common signature motif namely, Val or Thr at position 2 and positively charged residues Arg or Lys at the C-terminal anchor.. Allele A*74 : 01 : Presents immunodominant HIV-1 epitopes derived from gag-pol (GQMVHQAISPR, QIYPGIKVR) and rev (RQIHSISER), carrying an aliphatic residue at position 2 and Arg anchor residue at the C-terminus. May contribute to viral load control in chronic HIV-1 infection.
See full target information HLA-A

Additional targets

HLA-B,HLA-C

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