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Cell Survival Assays and Antibodies
Intracellular ThiolEZ™ Cell Survival Assay
Anti-BrdU Antibodies
Oxphos™ Cell Survival Assay
CellCountEZ™ Cell Survival Assay Kit
RadChemDosi™ Cell Survival Assay
Bromodeoxyuridine (5-bromo-2'-deoxyuridine, BrdU) is a synthetic thymidine nucleoside analog. BrdU is commonly used to allow the detection of growing or proliferating cells in living tissues.
BrdU Mouse Monoclonal Antibody
200-301-H50
BrdU Rabbit Polyclonal Antibody
600-401-C29
IdU Monoclonal Antibody
200-301-H51
CellCount EZ™
Best of XTT & WST
(Tetrazolium Salts)
Ease of Use
✔
-
Sensitivity of Detection
Reagent Stability
Instrumentation Burden
Total End User Cost to Perform Assay
Reproducibility of Date
ThiolEZ™
Best of totalthiol detection
(HPLC, biochemical assays)
Oxphos™
RadChemDosi™
Competitor Product
$3,600
The Mouse TrueBlot® Western Blot Kit contains the critical supporting reagents, buffers, and substrates for Akt immunoprecipitation and Western blotting of samples using TrueBlot second step immunoblotting reagents in conjunction with your own primary IP antibody and primary (Mouse IgG) Western blotting antibody. TrueBlot technology enables unhindered detection of protein bands of interest which would otherwise be obscured by the presence of reduced and denatured heavy and light chain immunoglobulin in the blot (as detected by the conventional immunoblotting HRP anti-mouse IgG reagent). Mouse IgG TrueBlot® ULTRA is the unique horseradish peroxidase conjugated anti-mouse IgG immunoblotting second step reagent which enables detection of Akt immunoblotted target protein bands, without hindrance by interfering immunoglobulin heavy and light chains from your IP antibody. Use it in place of your usual HRP anti-mouse IgG immunoblotting second step reagent. It is easy to generate publication-quality Akt IP Western Blot data with Mouse IgG TrueBlot® ULTRA.
Mouse IgG TrueBlot ULTRA is ideal for use in protocols involving immunoblotting of immunoprecipitated proteins. TrueBlot preferentially detects the non-reduced form of mouse IgG over the reduced, SDS-denatured form of IgG. When the immunoprecipitate is fully reduced immediately prior to SDS-gel electrophoresis, reactivity of Mouse IgG TrueBlot ULTRA with the 55 kDa heavy chains and the 23 kDa light chains of the immunoprecipitating antibody is minimized thereby eliminating interference by the heavy and light chains of the immunoprecipitating antibody in Akt IP Western Blotting applications. Applications include studies examining post-translational modification (e.g., phosphorylation or acetylation) or protein-protein interactions.
FOR LIFE SCIENCE RESEARCH USE ONLY