Fluorescein Goat Anti-Rabbit IgG Antibody can be used for immunofluorescence and other applications. Optimal F/P ratios have been established for each conjugate to ensure maximum fluorescence with minimal background staining.
|Unit Size||1.5 mg|
|Applications||Immunofluorescence, In situ hybridization, Blotting Applications, Flow Cytometry/Cell Separation|
|Concentration||1.5 mg active conjugate/ml|
|Recommended Storage||2-8 °C|
|Solution||10 mM HEPES, 0.15 M NaCl, pH 7.5, 0.08% sodium azide.|
|Maximum Emission||510-520 nm|
|Maximum Excitation||490-500 nm|
|Recommended Usage||The recommended concentration range for use is 5-20 µg/ml. If this fluorescein-labeled antibody is to be used in tissues which may contain cross-reacting endogenous immunoglobulins, dilution of this antibody may be made in buffers containing 2% normal serum from the same species as the tissue.|
|Color of Fluorescence||Green|
The goat anti-rabbit Ig antibodies are prepared by hyperimmunizing animals in a manner that produces high affinity antibodies. These are then purified by an affinity chromatography procedure designed to remove any low affinity antibodies which may be present. Cross-reactivities that are likely to interfere with specific labeling are removed by solid-phase adsorption techniques. The final product is then subjected to rigorous quality control assays including immunodiffusion, solid-phase enzyme immunoassays, gel electrophoresis and solid-phase binding assays. In preparing the labeled antibodies, great care is taken to ensure the maximum degree of labeling with no alteration in the specificity and affinity of the antibody. The labeled antibody then undergoes a further series of quality control assays, including immunohistochemical analysis.
Fluorescein Goat Anti-Rabbit IgG (H+L) Antibody can be used for flow cytometry or for tissue staining.
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