Rabbit Fab anti-Chicken IgG (H+L)-Biotin, MinX none

Artikelnummer: DNA-SEC-183922
Artikelname: Rabbit Fab anti-Chicken IgG (H+L)-Biotin, MinX none
Artikelnummer: DNA-SEC-183922
Hersteller Artikelnummer: SEC-183922
Alternativnummer: DNA-SEC-183922
Hersteller: dianova
Wirt: Rabbit
Kategorie: Antikörper
Applikation: ELISA,IHC,WB
Spezies Reaktivität: Gallus
Immunogen: Chicken IgG whole molecule
Konjugation: Biotin
Alternative Synonym: Rabbit Fab Anti-Chicken IgG Biotin Conjugated Antibody, Rabbit Fab Fragment Anti-Chicken IgG Antibody Biotin Conjugation, Rabbit Fab Anti-Chicken IgY Biotin Conjugated Antibody, Rabbit Fab Fragment Anti-Chicken IgY Antibody Biotin
Format: Fab
Spezifität: IgG (H+L)
Minimale Kreuzreaktivität (MinX): no cross-adsorbtion
Fab Anti-Chicken IgG Biotin Antibody generated in rabbit detects chicken IgY. This product possesses the F(ab) region possessing the epitope-recognition site, both heavy and light chains of the antibody molecule are present.
Klonalität: Polyclonal
Konzentration: 0.5 mg/mL
Isotyp: Ig
Puffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Reinheit: This product was prepared from monospecific antiserum by immunoaffinity chromatography using Chicken IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, papain digestion and chromatographic separation. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Biotin and anti-Rabbit Serum. No reaction was observed against anti-Papain or anti-Rabbit IgG F(c).
Formulierung: Lyophilized
Formel: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% NaN3
Target-Kategorie: Chicken
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 immunoblotting, ELISA, immunohistochemistry, immunomicroscopy as well as other antibody based assays using streptavidin or avidin conjugates requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.