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Immunohistochemistry Kits and Reagents
These products include a wide variety of immunohistochemistry kits and reagents for use in the immunohistochemical staining and analysis of tissue samples, including ELISAs, antibodies, tissue crosslinkers, fixatives, permeabilization reagents, molecular probes, dyes, and staining kits.
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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.
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
Features poly-HRP-conjugated goat anti-rabbit IgG secondary antibody. Alexa Fluor™ 488 Tyramide SuperBoost™ Kit combine brightness of AlexaFluor dyes with high signal amplification of a poly-HRP-mediated tyramide labeling reaction to produce s
Ultra-Sensitive ABC Peroxidase Rabbit IgG Staining Kit Thermo Scientific™
Thermo Scientific™ Pierce ABC Staining Kits include reagents for the avidin-biotin complex (ABC) technique, a highly sensitive method for immunohistochemical detection with biotinylated secondary antibodies.
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-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
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 to effectively suppress background fluorescence in live cell assays
CytoVista™ Antibody Dilution Buffer Invitrogen™
CytoVista Antibody Dilution Buffer is used to dilute the primary or secondary antibody when performing immunohistochemistry (IHC) or immuno-labeling with tissue or 3D cell cultures.
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.
Human Neural Stem Cell Immunocytochemistry Kit Invitrogen™
Human Neural Stem Cell Immunocytochemistry Kit
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-mouse IgG secondary antibody. Alexa Fluor™ 488 Tyramide SuperBoost™ Kit combine brightness of AlexaFluor dyes with high signal amplification of a poly-HRP-mediated tyramide labeling reaction to produce se
CytoVista™ Antibody Penetration Buffer Invitrogen™
CytoVista Antibody Penetration Buffer helps primary and secondary antibodies penetrate the cells of tissue or 3D cell culture when performing immunohistochemistry (IHC) or immuno-labeling.
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Life Technologies provides comprehensive sequencing kits and reagents developed specifically for each sequencing platform to enable the most efficient and effective sequencing results. Sanger sequencing kits and reagents support PCR amplification of region(s) of interest, cycle sequencing, and...
Preserving the integrity of your samples is critical to the success of every biobanking project. Biological samples must be prepared for a range of different research objectives and downstream analysis.
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Can I perform Click-iT EdU TUNEL detection on cells growing in 3D culture?
Phosphatase-Based Signal Amplification Techniques—Section 6.3