Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

Principle of the Procedure

This kit uses the Sandwich-ELISA principle. The microtiter plate strips has been pre-coated with an affinity purified antibody to Human AGR2. Standards or samples containing Human AGR2 are added to the plate and reacted with capture antibody. A second anti-Human AGR2 antibody labeled biotin is then added and binds to Human AGR2 captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Human AGR2-biotin labeled antibody-SA-HRP. And then, TMB substrate solution is added to all wells and incubated. An enzyme-catalyzed reaction generates a blue color in the solution, thereafter, stop solution is added to stop the substrate reaction and the color turns yellow. The yellow solution is read at a wavelength of 450nm. The concentration of Human AGR2 in the samples is then calculated from the OD value by establishing a standard curve.

Cat no: ABQ-ES96-AGR2hu
ABQ-ES96-AGR2hu
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

SKU

ABQ-ES96-AGR2hu

Applications

ELISA

Reactivity

Human

Alternative Name

Anterior gradient protein 2 homolog, AG2

Standard

10ng/mL.

Sensitivity

0.1 ng/mL.

Detection Range

0.16-10ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)

Principle of the Procedure

This kit uses the Sandwich-ELISA principle. The microtiter plate strips has been pre-coated with an affinity purified antibody to Human AGR2. Standards or samples containing Human AGR2 are added to the plate and reacted with capture antibody. A second anti-Human AGR2 antibody labeled biotin is then added and binds to Human AGR2 captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Human AGR2-biotin labeled antibody-SA-HRP. And then, TMB substrate solution is added to all wells and incubated. An enzyme-catalyzed reaction generates a blue color in the solution, thereafter, stop solution is added to stop the substrate reaction and the color turns yellow. The yellow solution is read at a wavelength of 450nm. The concentration of Human AGR2 in the samples is then calculated from the OD value by establishing a standard curve.

Cat no: ABQ-ES96-AGR2hu ABQ-ES96-AGR2hu Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

SKU

ABQ-ES96-AGR2hu

Applications

ELISA

Reactivity

Human

Alternative Name

Anterior gradient protein 2 homolog, AG2

Standard

10ng/mL.

Sensitivity

0.1 ng/mL.

Detection Range

0.16-10ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Product Name

Quanticon™ Human AGR2(Anterior Gradient Protein 2) ELISA Kit

SKU

ABQ-ES96-AGR2hu

Applications

ELISA

Reactivity

Human

Alternative Name

Anterior gradient protein 2 homolog, AG2

Standard

10ng/mL.

Sensitivity

0.1 ng/mL.

Detection Range

0.16-10ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-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