Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

Quanticon™ Rat α-Glu(Alpha Glucosidase) 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 Rat α-Glu. Standards or samples containing Rat α-Glu are added to the plate and reacted with capture antibody. A second anti-Rat α-Glu antibody labeled biotin is then added and binds to Rat α-Glu captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Rat α-Glu-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 Rat α-Glu in the samples is then calculated from the OD value by establishing a standard curve.

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

Product Name

Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

SKU

ABQ-ES96-AGLUrt

Applications

ELISA

Reactivity

Rat

Alternative Name

α-Glu

Standard

100ng/mL

Sensitivity

0.94 ng/mL.

Detection Range

1.57-100ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 μL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations

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Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
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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 Rat α-Glu. Standards or samples containing Rat α-Glu are added to the plate and reacted with capture antibody. A second anti-Rat α-Glu antibody labeled biotin is then added and binds to Rat α-Glu captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Rat α-Glu-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 Rat α-Glu in the samples is then calculated from the OD value by establishing a standard curve.

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

Product Name

Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

SKU

ABQ-ES96-AGLUrt

Applications

ELISA

Reactivity

Rat

Alternative Name

α-Glu

Standard

100ng/mL

Sensitivity

0.94 ng/mL.

Detection Range

1.57-100ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 μL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations

Product Name

Quanticon™ Rat α-Glu(Alpha Glucosidase) ELISA Kit

SKU

ABQ-ES96-AGLUrt

Applications

ELISA

Reactivity

Rat

Alternative Name

α-Glu

Standard

100ng/mL

Sensitivity

0.94 ng/mL.

Detection Range

1.57-100ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 μL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations

Our latest product

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