Vector Lab代理Horse Anti-Mouse IgG Antibody (H+L), Fluorescein

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Horse Anti-Mouse IgG Antibody (H+L), Fluorescein

FI-2000-1.5

SKU Unit Size Price Qty
FI-2000-1.5 1.5 mg

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Horse Anti-Mouse IgG Antibody (H+L), Fluorescein

Description
Specifications
Documents
Related Products
Citations
Technical Information

Description

Fluorescein Horse Anti-Mouse IgG Antibody can be used for tissue staining or other applications. Optimal F/P ratios have been established for each conjugate to ensure maximum fluorescence with minimal background staining.

Features:

  • Affinity-purified, ultrapure, high affinity antibody 
  • Thoroughly adsorbed against serum and immunoglobulins from potentially interfering species 
  • Recognizes both heavy and light chains (H+L) 
  • Optimally labeled with fluorescein to provide the brightest label for fluorescence microscopy 
  • Supplied in solution 
  • Excitation: 495 nm 
  • Emission: 515 nm 
  • Color: Green

Specifications

More Information
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 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.
Target Species Mouse
Conjugate Fluorescein
Color of Fluorescence Green
Host Species Horse
Format Concentrate

Documents

  • Safety Data Sheet
  • Download CoA
  • Datasheet

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Citations

Horse Anti-Mouse IgG Antibody (H+L), Fluorescein Powered by Bioz See more details on Bioz

Technical Information

The anti-mouse 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. 

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