HLA-Aw32 & HLA-A25 (MHC I)(CATA-1), 1mg/mL, Clone: [CATA-1], Mouse, Monoclonal

Artikelnummer: BOT-BNUM1073-50
Artikelname: HLA-Aw32 & HLA-A25 (MHC I)(CATA-1), 1mg/mL, Clone: [CATA-1], Mouse, Monoclonal
Artikelnummer: BOT-BNUM1073-50
Hersteller Artikelnummer: BNUM1073-50
Alternativnummer: BOT-BNUM1073-50-50UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: IHC
Spezies Reaktivität: Human
Immunogen: Normal human peripheral blood lymphocytes of phenotype A1, Aw32, B7, B37, Cw-, Cw-, DR2, DRw10
Alternative Synonym: HLA-A, HLA class 1A, MHC class I HLA-A
This MAb reacts with cells bearing HLA-A25 or HLA-Aw32 antigens. In addition, a reaction was observed with a cell of phenotype A2, Aw31, B17, Bw49. HLA-A, with HLA-B and HLA-C, belongs to major histocompatibility complex (MHC) class I antigens and expresses constitutively on all nucleated cells. HLA system comprises closely linked genes controlling highly polymorphic proteins involved in the presentation of peptides to the T-cell receptor, inhibition of NK cell cytotoxicity, and rejection of tissue allotransplantation. Specific alleles at HLA loci are associated with diseases. This MAb is specifically applicable for typing peripheral T cells for the antigens HLA-A25 and HLA-Aw32.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Klonalität: Monoclonal
Konzentration: 1 mg/mL
Klon-Bezeichnung: [CATA-1]
Molekulargewicht: kDa
UniProt: P01889
Puffer: PBS, no BSA, no azide
Quelle: Animal
Anwendungsbeschreibung: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 0.5-1 ug/mL|Immunohistology formalin-fixed 0.5-1 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Optimal dilution for a specific application should be determined by user