ELK7842-48T, ABA(Abscisic Acid) ELISA Kit, 48T

ELK7842-48T, ABA(Abscisic Acid) ELISA Kit, 48T

ELK7843-48T, Human Anti-C1q(Anti-Complement 1q Antibody) ELISA Kit, 48T

ELK7843-48T, Human Anti-C1q(Anti-Complement 1q Antibody) ELISA Kit, 48T

ELK7842-96T, ABA(Abscisic Acid) ELISA Kit, 96T

2.475,20 RON

ABA(Abscisic Acid) ELISA Kit

SKU
ELK7842-96T

Alternative Names: AB-A; abscisin II; Dormin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.54 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: tissue or cell culture supernates

Assay length: 2h

Research Area: Metabolic pathway;Hormone metabolism;

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

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Description

Alternative Names: AB-A; abscisin II; Dormin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.54 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: tissue or cell culture supernates

Assay length: 2h

Research Area: Metabolic pathway;Hormone metabolism;

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