Donkey anti-Rat IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ Plus 647, Invitrogen™

Description

To minimize cross-reactivity, the donkey anti-rat IgG whole antibodies have been cross-adsorbed against serum proteins from bovine, goat, rabbit, mouse, chicken, guinea pig, hamster, horse, sheep, and human to increase specificity of the antibody resulting in less background staining and cross-reactivity. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. Further passages through additional columns result in highly cross-adsorbed preparations of secondary antibody. The benefits of these extra steps are apparent in multiplexing/multicolor-staining experiments where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins. Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment to eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining.. This antibody binds to heavy chains on rat IgG and light chains on all rat immunoglobulins, does not bind non-immunoglobulin rat serum proteins or IgG from bovine, goat, rabbit, mouse, chicken, guinea pig, hamster, horse, sheep, or human.

Anti-Rat secondary antibodies are affinity-purified antibodies with well-characterized specificity for rat immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.