ELK0213-96T, Zebrafish GH(Growth Hormone) ELISA Kit, 96T

ELK0213-96T, Zebrafish GH(Growth Hormone) ELISA Kit, 96T

ELK0214-96T, Rat GAPDH(Glyceraldehyde-3-Phosphate Dehydrogenase) ELISA Kit, 96T

ELK0214-96T, Rat GAPDH(Glyceraldehyde-3-Phosphate Dehydrogenase) ELISA Kit, 96T

ELK0214-48T, Rat GAPDH(Glyceraldehyde-3-Phosphate Dehydrogenase) ELISA Kit, 48T

2.142,00 RON

Rat GAPDH(Glyceraldehyde-3-Phosphate Dehydrogenase) ELISA Kit

SKU
ELK0214-48T

Alternative Names: G3PD; GAPD; Peptidyl-cysteine S-nitrosylase GAPDH

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.067 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Metabolic pathway;Cardiovascular biology;Hepatology;Nutrition metabolism;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat GAPDH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GAPDH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat GAPDH, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat GAPDH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: G3PD; GAPD; Peptidyl-cysteine S-nitrosylase GAPDH

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.067 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Metabolic pathway;Cardiovascular biology;Hepatology;Nutrition metabolism;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat GAPDH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GAPDH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat GAPDH, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat GAPDH in the samples is then determined by comparing the OD of the samples to the standard curve.