ELK1917-96T, Human NAGase(N-Acetyl Beta-D-Glucosaminidase) ELISA Kit, 96T

ELK1917-96T, Human NAGase(N-Acetyl Beta-D-Glucosaminidase) ELISA Kit, 96T

ELK1918-96T, Human ACVAB(Activin AB) ELISA Kit, 96T

ELK1918-96T, Human ACVAB(Activin AB) ELISA Kit, 96T

ELK1918-48T, Human ACVAB(Activin AB) ELISA Kit, 48T

2.142,00 RON

Human ACVAB(Activin AB) ELISA Kit

SKU
ELK1918-48T

Alternative Names: ACV-AB; Activin Beta A Beta B Homodimer

Species: Human

Assay Type: Sandwich

Sensitivity: 5.6 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

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

Assay length: 3.5h

Research Area: Endocrinology;Reproductive science;Hormone metabolism;

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

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Description

Alternative Names: ACV-AB; Activin Beta A Beta B Homodimer

Species: Human

Assay Type: Sandwich

Sensitivity: 5.6 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

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

Assay length: 3.5h

Research Area: Endocrinology;Reproductive science;Hormone metabolism;

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