TAE buffer(50X)

TAE buffer(50X)

Tris-acetate-EDTA (TAE) Buffer is designed to be used in molecular biology for agarose gel electrophoresis to separate nucleic acids like DNA and RNA. It consists of Tris base , acetic acid , and EDTA ,functioning as both a running buffer and a gel preparation buffer. It maintains pH around 8.3 and protects DNA degradation during run. eliminates DNAse activity TAE is particularly suited for the separation of a broad range of DNA fragments, especially for preparative electrophoresis and cloning experiments.

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TAE buffer(50X)

TAE buffer(50X)

TAE buffer(50X)

Tris-acetate-EDTA (TAE) Buffer is designed to be used in molecular biology for agarose gel electrophoresis to separate nucleic acids like DNA and RNA. It consists of Tris base , acetic acid , and EDTA ,functioning as both a running buffer and a gel preparation buffer. It maintains pH around 8.3 and protects DNA degradation during run. eliminates DNAse activity TAE is particularly suited for the separation of a broad range of DNA fragments, especially for preparative electrophoresis and cloning experiments.

Cat no: TAE50 TAE50 Size: Rate Rate 500ml: $60 $60 100ml: $15 $15 Datasheet Get Quote MS/DS COA

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Principle of the Procedure

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig CCK. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig CCK. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Pig CCK in the samples is then determined by comparing the OD of the samples to the standard curve.

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