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

Catalog Number: DNA-SEC-183921
Article Name: Rabbit Fab anti-Chicken IgG (H+L)-HRPO, MinX none
Biozol Catalog Number: DNA-SEC-183921
Supplier Catalog Number: SEC-183921
Alternative Catalog Number: DNA-SEC-183921
Manufacturer: dianova
Host: Rabbit
Category: Antikörper
Application: ELISA,IHC,WB
Species Reactivity: Gallus
Immunogen: Chicken IgG whole molecule
Conjugation: HRPO
Alternative Names: Rabbit Fab Anti-Chicken IgG Antibody Peroxidase Conjugation, Rabbit Fab Anti-Chicken IgG HRP Conjugated Antibody, Rabbit Fab Anti-Chicken IgY Antibody Peroxidase Conjugation, Rabbit Fab Anti-Chicken IgY HRP
Format: Fab
Target Specificity: IgG (H+L)
Cross-Adsorption (MinX): no cross-adsorbtion
Fab Anti-Chicken IgG Peroxidase 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.
Clonality: Polyclonal
Concentration: 1.0 mg/mL
Isotype: Ig
Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Purity: 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-Peroxidase and anti-Rabbit Serum. No reaction was observed against anti-Papain or anti-Rabbit IgG F(c).
Form: Lyophilized
Formula: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% Gentamicin
Target: Chicken
Antibody Type: Secondary Antibody
Application Dilute: ELISA Dilution: 1:10,000 - 1:40,000, Immunohistochemistry Dilution: 1:500 - 1:2,500, Western Blot Dilution: 1:1,000 - 1:4,000
Application Notes: Suitable for immunoblotting (western or dot blot), ELISA, immunoperoxidase electron microscopy and immunohistochemistry as well as other peroxidase-antibody based enzymatic assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.