ELK3241-96T, Rat APC(Activated Protein C) ELISA Kit, 96T

ELK3241-96T, Rat APC(Activated Protein C) ELISA Kit, 96T

ELK3242-96T, Human CHGB(Chromogranin B) ELISA Kit, 96T

ELK3242-96T, Human CHGB(Chromogranin B) ELISA Kit, 96T

ELK3242-48T, Human CHGB(Chromogranin B) ELISA Kit, 48T

2.142,00 RON

Human CHGB(Chromogranin B) ELISA Kit

SKU
ELK3242-48T

Alternative Names: SCG1; CgB; SgI; Secretoneurin 1; Secretogranin 1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.255 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

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

Assay length: 3.5h

Research Area: Neuro science;

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

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Description

Alternative Names: SCG1; CgB; SgI; Secretoneurin 1; Secretogranin 1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.255 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

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

Assay length: 3.5h

Research Area: Neuro science;

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