ELK8753-96T, Plant IAA(Indole 3 Acetic Acid) ELISA Kit, 96T

ELK8753-96T, Plant IAA(Indole 3 Acetic Acid) ELISA Kit, 96T

ELK8754-96T, Plant GA(Gibberellic Acid) ELISA Kit, 96T

ELK8754-96T, Plant GA(Gibberellic Acid) ELISA Kit, 96T

ELK8754-48T, Plant GA(Gibberellic Acid) ELISA Kit, 48T

1.814,75 RON

Plant GA(Gibberellic Acid) ELISA Kit

SKU
ELK8754-48T

Alternative Names: GA3; Gibberellin A3; Gibberellins

Species: Plant

Assay Type: Competitive Inhibition

Sensitivity: 52.1 ng/mL

Standard: 10000 ng/mL

Detection range: 156.25-10000 ng/mL

Sample type: plant tissues

Assay length: 2h

Research Area: Nutrition metabolism;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 Plant GA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Plant GA. 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 Plant GA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: GA3; Gibberellin A3; Gibberellins

Species: Plant

Assay Type: Competitive Inhibition

Sensitivity: 52.1 ng/mL

Standard: 10000 ng/mL

Detection range: 156.25-10000 ng/mL

Sample type: plant tissues

Assay length: 2h

Research Area: Nutrition metabolism;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 Plant GA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Plant GA. 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 Plant GA in the samples is then determined by comparing the OD of the samples to the standard curve.