Quanticon™ Rat FSH(Follicle Stimulating Hormone) ELISA Kit

Quanticon™ Rat FSH(Follicle Stimulating Hormone) ELISA Kit

Principle of the Procedure

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

Cat no: ABQK-ES96-FSHrt
ABQK-ES96-FSHrt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Rat FSH(Follicle Stimulating Hormone)

ELISA Kit

SKU

ABQK-ES96-FSHrt

Applications

ELISA

Reactivity

Rat

Alternative Name

FSH-B, FSH-beta

Standard

100 mIU/mL

Sensitivity

0.72 mIU/mL

Detection Range

1.57-100 mIU/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, and Cell culture supernatants and other biological fluids

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Rat FSH(Follicle Stimulating Hormone) ELISA Kit

Quanticon™ Rat FSH(Follicle Stimulating Hormone) ELISA Kit

Quanticon™ Rat FSH(Follicle Stimulating Hormone) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)
Principle of the ProcedureThe 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 FSH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat FSH. 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 FSH, 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 FSH in the samples is then determined by comparing the OD of the samples to the standard curve. Cat no: ABQK-ES96-FSHrt ABQK-ES96-FSHrt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ Rat FSH(Follicle Stimulating Hormone)ELISA Kit
SKUABQK-ES96-FSHrt
ApplicationsELISA
ReactivityRat
Alternative Name FSH-B, FSH-beta
Standard 100 mIU/mL
Sensitivity0.72 mIU/mL
Detection Range1.57-100 mIU/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, and Cell culture supernatants and other biological fluids
Sample Volume100 ÎĽL
Assay TypeSandwich
Assay Duration3.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ Rat FSH(Follicle Stimulating Hormone)ELISA Kit
SKUABQK-ES96-FSHrt
ApplicationsELISA
ReactivityRat
Alternative Name FSH-B, FSH-beta
Standard 100 mIU/mL
Sensitivity0.72 mIU/mL
Detection Range1.57-100 mIU/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, and Cell culture supernatants and other biological fluids
Sample Volume100 ÎĽL
Assay TypeSandwich
Assay Duration3.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations

Principle of the Procedure

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

Citations  Â