ELK7367-96T, Mouse CLIC1(Chloride Intracellular Channel Protein 1) ELISA Kit, 96T

ELK7367-96T, Mouse CLIC1(Chloride Intracellular Channel Protein 1) ELISA Kit, 96T

ELK7368-96T, Rat NMU(Neuromedin U) ELISA Kit, 96T

ELK7368-96T, Rat NMU(Neuromedin U) ELISA Kit, 96T

ELK7368-48T, Rat NMU(Neuromedin U) ELISA Kit, 48T

2.142,00 RON

Rat NMU(Neuromedin U) ELISA Kit

SKU
ELK7368-48T

Alternative Names: NM-U

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 48.2 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: Endocrinology;Cardiovascular biology;Neuro science;Gastroenterology;Hormone metabolism;Bone 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 NMU protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NMU. 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 NMU 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-U

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 48.2 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: Endocrinology;Cardiovascular biology;Neuro science;Gastroenterology;Hormone metabolism;Bone 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 NMU protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NMU. 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 NMU in the samples is then determined by comparing the OD of the samples to the standard curve.