Bovine Purkinje cell protein 4- like protein 1, PCP4L1 ELISA KIT

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  • Model: ELI-22835b
  • 20 Units in Stock
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Bovine Purkinje cell protein 4- like protein 1, PCP4L1 ELISA KIT

Product Name:Bovine Purkinje cell protein 4- like protein 1, PCP4L1 ELISA KIT
Packing:96T

Catalog No.:ELI-22835b

Gene Name:Bovine Purkinje cell protein 4-like protein 1, PCP4L1

Detect Range:78-5000pg/ml

Sensitivity:46.9pg/ml

Target Protein Name:Bovine Purkinje cell protein 4-like protein 1, PCP4L1

Alternative Name:PCP4L1,Bovine Purkinje cell protein 4-like protein 1, PCP4L1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA type:Sandwich ELISA Kit
Product Description:Bovine Purkinje cell protein 4- like protein 1, PCP4L1 ELISA KIT allows for the in vitro quantitative determination of Bovine Purkinje cell protein 4-like protein 1, PCP4L1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA Test Principle:
The microtiter plate provided in Bovine Purkinje cell protein 4- like protein 1, PCP4L1 ELISA KIT has been pre-coated with an Bovine Purkinje cell protein 4-like protein 1, PCP4L1 antibody specific to Bovine Purkinje cell protein 4-like protein 1, PCP4L1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Purkinje cell protein 4-like protein 1, PCP4L1 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 Purkinje cell protein 4-like protein 1, PCP4L1, 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 Purkinje cell protein 4-like protein 1, PCP4L1 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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