Color of Fluorescence Blue | |
Format Concentrate | |
Formulation 10 mM HEPES, 0.15 M NaCl, pH 7.5, 0.08% sodium azide | |
Maximum Emission 448-454 nm. | |
Maximum Excitation 345-355 nm | |
Unit Size 1.5 mg | |
Storage Instructions 2-8 °C | |
Usage Summary The recommended concentration range for use is 5-20 µg/ml | |
Applications Immunofluorescence, In situ hybridization, Flow Cytometry/Cell Separation | |
Target Species Rabbit | |
Concentration 1.5 mg active conjugate/ml | |
Conjugate AMCA | |
Reactive Species Goat | |
Source Species Rabbit | |
Host Species Goat |
-
This product has been discontinued.
Please consider the following as potential substitutes: DI-1088-1.5. Horse Anti-Rabbit IgG Antibody (H+L), DyLight™ 488. Or contact Technical Support @ [email protected] for assistance in finding alternative.
Goat Anti-Rabbit IgG Antibody (H+L)
AMCA 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.
Features:
• Recognizes both heavy and light chains (H+L)
• Optimally labeled with AMCA to provide the brightest label for fluorescence microscopy
• Supplied in solution
• Excitation: 350 nm
• Emission: 450 nm
• Color: Blue
$205.00
| SKU | Unit Size | Price |
|---|---|---|
Select a unit size:
How do I request a quote or bulk pricing?
Technical Information 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. |
Citations |


