ELK6815-48T, Rat AP13(Apelin 13) ELISA Kit, 48T

ELK6815-48T, Rat AP13(Apelin 13) ELISA Kit, 48T

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ELK6816-48T, Rat GLUT3(Glucose Transporter 3) ELISA Kit, 48T

ELK6815-96T, Rat AP13(Apelin 13) ELISA Kit, 96T

2.963,10 RON

Rat AP13(Apelin 13) ELISA Kit

SKU
ELK6815-96T

Alternative Names: APLN13

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 26.38 pg/mL

Standard: 6000 pg/mL

Detection range: 93.75-6000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Neuro science;Gastroenterology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat AP13 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat AP13. 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 Rat AP13 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: APLN13

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 26.38 pg/mL

Standard: 6000 pg/mL

Detection range: 93.75-6000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Neuro science;Gastroenterology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat AP13 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat AP13. 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 Rat AP13 in the samples is then determined by comparing the OD of the samples to the standard curve.