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HLA-DP/DQ/DR Antibody / Pan-HLA

Reacts with a common epitope of human major histocompatibility (MHC) class II antigens, HLA-DP, -DQ and -DR. Human MHC class II antigens are transmembrane glycoproteins composed of an alpha chain (36kDa) and a beta chain (27kDa) . They are expressed primarily on antigen presenting cells such as B lymphocytes, monocytes, macrophages, and thymic epithelial cells and are also present on activated T lymphocytes. Human MHC class II genes are located in the HLA-D region that encodes at least six alpha and ten beta chain genes. Three loci, DR, DQ and DP, encode the major expressed products of the human class II region. The human MHC class II molecules bind intracellularly processed peptides and present them to T-helper cells. They, therefore, have a critical role in the initiation of the immune response.

Product Specifications

CAS Number

9000-83-3

Specifications

Immunohistochemistry (FFPE) : 1-2 µg/mL for 30 min at RT

UniProt

P04440, P01908, P01909, P01920, P01903

Host

Rabbit

Reactivity

Human

Immunogen

Priess cells (a human B cell line) were used as the immunogen for the HLA-DP/DQ/DR antibody.

Clonality

Recombinant Monoclonal

Isotype

IgG κ

Clone

HLA-Pan/8622R

Type

Recombinant

Applications

IHC-P

Purity

Protein A/G affinity

Format

Purified

Buffer

0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide

Reconstitution

Aliquot the HLA-DP/DQ/DR antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Limitations

This HLA-DP/DQ/DR antibody is available for research use only.

Storage Conditions

Aliquot the HLA-DP/DQ/DR antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Formulation

0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05% sodium azide

Applications Notes

Optimal dilution of the HLA-DP/DQ/DR antibody should be determined by the researcher.

Location

Cell Surface

Image Legend

IHC staining of FFPE human tonsil tissue with HLA-DP/DQ/DR antibody (clone HLA-Pan/8622R) . Inset: PBS used in place of primary Ab (secondary Ab negative control) . HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.

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