A wide variety of immunoassays, reagents, and kits for use in the immunohistochemical staining and analysis of tissue samples. Includes ELISAs, antibodies, tissue crosslinkers, fixatives, permeabilization reagents, molecular probes, dyes, and staining kits.
SuperBoost™ tyramide signal amplification is the most sensitive method for detection of low abundant targets in multiplexable fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC ), and in situ hybridization (ISH).
Features poly-HRP-conjugated goat anti-rabbit IgG secondary antibody. Alexa Fluor™ 647 Tyramide SuperBoost™ Kit combine brightness of AlexaFluor dyes with high signal amplification of a poly-HRP-mediated tyramide labeling reaction to produce s
SuperBoost™ tyramide signal amplification is the most sensitive method for detection of low abundant targets in multiplexable fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC ), and in situ hybridization (ISH).
Designed for use during the heat induced epitope retrieval (HIER) step prior to immunohistochemistry on formalin-fixed paraffin-embedded tissue sections. Used in combination with heat has been shown to restore the antigenicity of proteins modified during the formalin fixation of tissue.
Designed for use during the heat induced epitope retrieval (HIER) step prior to immunohistochemistry on formalin-fixed paraffin embedded tissue sections. Use in combination with heat has been shown to restore the antigenicity of proteins modified during the formalin fixation of tissue.
Minimizes unwanted autofluorescence in FFPE and frozen tissues due to aldehyde fixation, red blood cells, and structural elements such as collagen and elastin
Features poly-HRP-conjugated goat anti-mouse IgG secondary antibody. Alexa Fluor™ 647 Tyramide SuperBoost™ Kit combine brightness of AlexaFluor dyes with high signal amplification of a poly-HRP-mediated tyramide labeling reaction to produce se
Contains the necessary reagents and buffers for identifying and examining proliferating cells by immunohistochemical or immunocytochemical analysis. Optimized for IHC with both frozen and paraffin-embedded BrdU-labeled mouse intestine and ICC of BrdU-pulsed HeLa cells grown on culture slides.