ELK1042-48T, BSA(Bovine Serum Albumin) ELISA Kit, 48T

ELK1042-48T, BSA(Bovine Serum Albumin) ELISA Kit, 48T

ELK1043-48T, Human IFNa(Interferon Alpha) ELISA Kit, 48T

ELK1043-48T, Human IFNa(Interferon Alpha) ELISA Kit, 48T

ELK1042-96T, BSA(Bovine Serum Albumin) ELISA Kit, 96T

2.475,20 RON

BSA(Bovine Serum Albumin) ELISA Kit

SKU
ELK1042-96T

Alternative Names: Bovine Albumin; Fraction V

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 161.2 ng/mL

Standard: 30000 ng/mL

Detection range: 468.75-30000 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Immune molecule;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with BSA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to BSA. 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 BSA in the samples is then determined by comparing the OD of the samples to the standard curve.

Mai multe informatii
Price 2.080,00 RON (preturile sunt fara TVA)
Description

Alternative Names: Bovine Albumin; Fraction V

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 161.2 ng/mL

Standard: 30000 ng/mL

Detection range: 468.75-30000 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Immune molecule;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with BSA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to BSA. 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 BSA in the samples is then determined by comparing the OD of the samples to the standard curve.