Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) 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 AMBP. Standards or samples containing Human AMBP are added to the plate and reacted with capture antibody. A second anti-Human AMBP antibody labeled biotin is then added and binds to Human AMBP captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Human AMBP-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 AMBP in the samples is then calculated from the OD value by establishing a standard curve.

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

Product Name

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

SKU

ABQ-ES96-AMBPhu

Applications

ELISA

Reactivity

Human

Alternative Name

Protein AMBP, alpha-1-microglobulin (A1M), Protein HC, Bikunin

Standard

300ng/mL.

Sensitivity

2.81 ng/mL.

Detection Range

4.69-300ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

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

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

Product Name

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

SKU

ABQ-ES96-AMBPhu

Applications

ELISA

Reactivity

Human

Alternative Name

Protein AMBP, alpha-1-microglobulin (A1M), Protein HC, Bikunin

Standard

300ng/mL.

Sensitivity

2.81 ng/mL.

Detection Range

4.69-300ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Product Name

Quanticon™ Human AMBP(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

SKU

ABQ-ES96-AMBPhu

Applications

ELISA

Reactivity

Human

Alternative Name

Protein AMBP, alpha-1-microglobulin (A1M), Protein HC, Bikunin

Standard

300ng/mL.

Sensitivity

2.81 ng/mL.

Detection Range

4.69-300ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

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