Bovine Protein farnesyltransferase subunit beta, FNTB ELISA KIT

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  • Model: ELI-30850b
  • 20 Units in Stock
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Bovine Protein farnesyltransferase subunit beta, FNTB ELISA KIT

Product Name:Bovine Protein farnesyltransferase subunit beta, FNTB ELISA KIT
Packing:96T

Catalog No.:ELI-30850b

Gene Name:Bovine Protein farnesyltransferase subunit beta, FNTB

Detect Range:15.625-1000pg/ml

Sensitivity:9.375pg/ml

Target Protein Name:Bovine Protein farnesyltransferase subunit beta, FNTB

Alternative Name:FNTB,Bovine Protein farnesyltransferase subunit beta, FNTB
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA type:Sandwich ELISA Kit
Product Description:Bovine Protein farnesyltransferase subunit beta, FNTB ELISA KIT allows for the in vitro quantitative determination of Bovine Protein farnesyltransferase subunit beta, FNTB concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA Test Principle:
The microtiter plate provided in Bovine Protein farnesyltransferase subunit beta, FNTB ELISA KIT has been pre-coated with an Bovine Protein farnesyltransferase subunit beta, FNTB antibody specific to Bovine Protein farnesyltransferase subunit beta, FNTB .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Protein farnesyltransferase subunit beta, FNTB and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Bovine Protein farnesyltransferase subunit beta, FNTB, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.The concentration of Bovine Protein farnesyltransferase subunit beta, FNTB in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!

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