ELK6862-96T, Dog HP(Haptoglobin) ELISA Kit, 96T

ELK6862-96T, Dog HP(Haptoglobin) ELISA Kit, 96T

ELK6863-96T, Rat ADH(Antidiuretic Hormone) ELISA Kit, 96T

ELK6863-96T, Rat ADH(Antidiuretic Hormone) ELISA Kit, 96T

ELK6863-48T, Rat ADH(Antidiuretic Hormone) ELISA Kit, 48T

2.142,00 RON

Rat ADH(Antidiuretic Hormone) ELISA Kit

SKU
ELK6863-48T

Alternative Names: ARVP; AVP; VP; Arginine Vasopressin; Arg-Vasopressin; Antidiuretic Hormone; Diabetes Insipidus; Neurohypophyseal; Argipressin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 4.63 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;Endocrinology;Neuro science;Hormone metabolism;Urology;

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

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Description

Alternative Names: ARVP; AVP; VP; Arginine Vasopressin; Arg-Vasopressin; Antidiuretic Hormone; Diabetes Insipidus; Neurohypophyseal; Argipressin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 4.63 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;Endocrinology;Neuro science;Hormone metabolism;Urology;

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