ELK1924-96T, Human aMSH(Alpha-Melanocyte Stimulating Hormone) ELISA Kit, 96T

ELK1924-96T, Human aMSH(Alpha-Melanocyte Stimulating Hormone) ELISA Kit, 96T

ELK1925-96T, Human PON1(Paraoxonase 1) ELISA Kit, 96T

ELK1925-96T, Human PON1(Paraoxonase 1) ELISA Kit, 96T

ELK1925-48T, Human PON1(Paraoxonase 1) ELISA Kit, 48T

2.142,00 RON

Human PON1(Paraoxonase 1) ELISA Kit

SKU
ELK1925-48T

Alternative Names: ESA; PON; Esterase A; Serum paraoxonase/arylesterase 1; Aromatic esterase 1; A-esterase 1; Serum aryldialkylphosphatase 1

Species: Human

Assay Type: Sandwich

Sensitivity: 1.27 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;Endocrinology;

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 Human PON1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PON1. 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 Human PON1, 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 Human PON1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ESA; PON; Esterase A; Serum paraoxonase/arylesterase 1; Aromatic esterase 1; A-esterase 1; Serum aryldialkylphosphatase 1

Species: Human

Assay Type: Sandwich

Sensitivity: 1.27 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;Endocrinology;

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 Human PON1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PON1. 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 Human PON1, 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 Human PON1 in the samples is then determined by comparing the OD of the samples to the standard curve.