Goat F(ab)2 anti-Human IgA-unconj., MinX none

Artikelnummer: DNA-SEC-183723
Artikelname: Goat F(ab)2 anti-Human IgA-unconj., MinX none
Artikelnummer: DNA-SEC-183723
Hersteller Artikelnummer: SEC-183723
Alternativnummer: DNA-SEC-183723
Hersteller: dianova
Wirt: Goat
Kategorie: Antikörper
Applikation: ELISA,IHC,WB
Spezies Reaktivität: Human
Immunogen: Human IgA alpha heavy chain
Konjugation: Unconjugated
Alternative Synonym: Goat F(ab)2 anti-Human IgA (alpha chain) Antibody, Goat F(ab)2 anti-Human IgA alpha Antibody
Format: F(ab')2
Spezifität: IgA
Minimale Kreuzreaktivität (MinX): no cross-adsorbtion
F(ab)2 Anti-Human IgA Antibody generated in goat detects immunoglobulin A (alpha chain) from human. Immunoglobulin A (IgA) is an antibody that plays a critical role in mucosal immunity. IgA has two subclasses (IgA1 and IgA2) and can exist in a dimeric fo
Klonalität: Polyclonal
Konzentration: 1.3 mg/mL
Isotyp: Ig
Puffer: 10 mM NaPO4,250 mM NaCl,pH 7,2,steril filtriert,Azid-/BSA-frei
Reinheit: This product is supplied in 0.01M Sodium Phosphate, 0.25M Sodium Chloride, pH: 7.6. This product was prepared from monospecific antiserum by immunoaffinity chromatography using antigens coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation.   Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum, Human IgA and Human Serum.  No reaction was observed against anti-Pepsin or anti-Goat IgG F(c).  Specificity was confirmed by ELISA at less than 1% cross reactivity against other human heavy or light chain isotypes.
Formulierung: Liquid (sterile filtered)
Formel: 10 mM NaPO4,250 mM NaCl,pH 7,2,sterile filtered,Azide/BSA free
Target-Kategorie: Human
Antibody Type: Secondary Antibody
Application Verdünnung: ELISA Dilution: 1:20,000 - 1:100,000, Immunohistochemistry Dilution: 1:1,000 - 1:5,000, Western Blot Dilution: 1:2,000 - 1:10,000
Anwendungsbeschreibung: Suitable for highly specific immunological methods requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.