Peroxidase-Conjugated Goat IgG Fraction to Human Kappa Chain

Analysis Note The total protein is measured using the Biuret procedure with bovine albumin as the standard. To ensure that the product titer falls within the required range, antibody titer is standardized by microtiter plate ELISA with human kappa Fab. The product is tested for purity and specificity at final concentration by immunoelectrophoresis. Preparation Method Antibody and highly purified HRP (Rz>3.0) are conjugated under defined conditions to obtain optimally labeled product. Conjugated protein is purified by salt fractionation. The product is dialyzed into 0.02M sodium phosphate, 0.14M sodium chloride, pH 7.3, adjusted to standard titer, filtered through a 0.22 µm filter, vialed and lyophilized. Applications Peroxidase-Conjugated Goat IgG Fraction To Human Kappa Chain (Bound) is suitable for use as a reagent in enzyme immunoassays (EIA), cell and immunostaining of acetone-fixed frozen and formalin-fixed, paraffin-embedded tissue sections, cell and tissue labeling (for electron microscopy), and blot immunostaining. Product Description Peroxidase-Conjugated Goat IgG Fraction To Human Kappa Chain (Bound) is the lyophilized powder of horseradish peroxidase (HRP)-conjugated goat IgG fraction to human kappa light chain (bound) and buffer salts. Typical Working Concentration Dilution Recommended: 1:500 - 1:4,000 for Tissue Staining; 1:1,000 - 1:8,000 for Immuno Blotting; 1:2,000 - 1:16,000 for ELISA/FIA