ELK0175-48T, Rat ACV-A(Activin A) ELISA Kit, 48T

ELK0175-48T, Rat ACV-A(Activin A) ELISA Kit, 48T

ELK0176-48T, Pig MUC2(Mucin 2) ELISA Kit, 48T

ELK0176-48T, Pig MUC2(Mucin 2) ELISA Kit, 48T

ELK0175-96T, Rat ACV-A(Activin A) ELISA Kit, 96T

2.963,10 RON

Rat ACV-A(Activin A) ELISA Kit

SKU
ELK0175-96T

Alternative Names: ACVA; Activin Beta A Beta A Homodimer

Species: Rat

Assay Type: Sandwich

Sensitivity: 4.66 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma 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 Rat ACV-A. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ACV-A. 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 Rat ACV-A, 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 Rat ACV-A in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ACVA; Activin Beta A Beta A Homodimer

Species: Rat

Assay Type: Sandwich

Sensitivity: 4.66 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma 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 Rat ACV-A. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ACV-A. 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 Rat ACV-A, 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 Rat ACV-A in the samples is then determined by comparing the OD of the samples to the standard curve.