Anti-HLA-Pan (MHC II) Monoclonal Antibody(Clone: HLA-Pan/2967R)
Fig. 1: Formalin-fixed, paraffin-embedded human Tonsil stained with HLA-Pan Rabbit Recombinant Monoclonal Antibody (HLA-Pan/2967R).
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| Amount : | 100 µg |
| Isotype : | Rabbit IgG |
| Content : | 200 µg/ml of Ab Purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml. |
| Storage condition : | Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. |
| Gene : | HLA-DP; HLA-DQ; HLA-DR |
| Gene ID : | 3115; 3117; 3122 |
| Uniprot ID : | P04440; P01908; P01909; P01920; P01903 |
| Alternative Name : | HLA-DPB1; HLA-DQA1; HLA-DQB1; HLA-DRA; HLA-DRB1; HLA-DRB3; HLA-DRB4; HLA-DRB5 |
| Immunogen Information : | Non-T, non-B human acute lymphoblastic leukemia REH6 cell line |
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 chain (36kDa) and a 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 and ten 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. It has been shown that some autoimmune diseases are associated with certain class II alleles.
ELISA (For coating use Ab at 2-5µg/ml, order Ab without BSA); Flow Cytometry (1-2µg/million cells); ,Immunofluorescence (1-2µg/ml). Western Blot (1-2µg/ml);Immunohistochemistry (Formalin-fixed) (1-2µg/ml for 30 minutes at RT),(Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Citrate Buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes)
For Research Use Only. Not for use in diagnostic/therapeutics procedures.
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