When an unconjugated primary antibody is made in the same species as your tissue specimen, subsequent detection using a secondary antibody usually generates high background staining and interference due to the inability of the secondary antibody to distinguish between the primary antibody (immunoglobulin) and endogenous immunoglobulins. This high background obscures target antigen specific staining and often leads to false positive staining.
Vector Laboratories offers solutions for two often encountered species on species scenarios:
Are specifically designed for detecting and visualizing (unconjugated) mouse primary antibodies in mouse tissue specimens. These kits contain a proprietary reagent that blocks endogenous mouse Ig in specimens therefore preventing non-specific binding of subsequent anti-mouse IgG detection reagents.
Our Mouse on Mouse kits significantly reduce endogenous mouse Ig staining when applying mouse antibodies on mouse specimens (e.g. tissue sections and cell preparations).
Additionally, these kits:
- Contain proprietary M.O.M. Mouse IgG Blocking Reagent
- Employ either avidin-biotin or polymer technology
- Are compatible with fluorescent or enzyme-based detection
- Are available with or without enzyme or fluorochrome
Is intended to detect human (or humanized) antibodies on frozen or paraffin embedded human tissue sections. This kit employs a straightforward two-step primary antibody preparation followed by standard IHC assay detection procedures to eliminate confounding interference from endogenous human IgG.
The VECTOR Human on Human Immunodetection Kit (HOH-3000) significantly reduces endogenous human Ig staining when applying human (or humanized) primary antibodies on human tissue sections.
Additionally, this kit:
- Is a comprehensive HRP (peroxidase) kit with volume matched reagents and ImmPACT DAB EqV substrate
- Does not require tedious antibody dilution calculations
- Enables staining results in about 90 mins following initial preparation
- Provides essentially background-free staining on frozen and paraffin-embedded human tissue sections