ELK4997-48T, Rat NMB(Neuromedin B) ELISA Kit, 48T

ELK4997-48T, Rat NMB(Neuromedin B) ELISA Kit, 48T

ELK4998-48T, Mouse GDH(Glutamate Dehydrogenase 1) ELISA Kit, 48T

ELK4998-48T, Mouse GDH(Glutamate Dehydrogenase 1) ELISA Kit, 48T

ELK4997-96T, Rat NMB(Neuromedin B) ELISA Kit, 96T

2.963,10 RON

Rat NMB(Neuromedin B) ELISA Kit

SKU
ELK4997-96T

Alternative Names: NM-B

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 43.6 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Endocrinology;Neuro science;Gastroenterology;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 Rat NMB protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NMB. 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 NMB in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: NM-B

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 43.6 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Endocrinology;Neuro science;Gastroenterology;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 Rat NMB protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NMB. 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 NMB in the samples is then determined by comparing the OD of the samples to the standard curve.