Quanticon™ Human CASP7(Caspase 7) ELISA Kit

Quanticon™ Human CASP7(Caspase 7) 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 CASP7. Standards or samples containing Human CASP7 are added to the plate and reacted with capture antibody. A second anti-Human CASP7 antibody labeled biotin is then added and binds to Human CASP7 captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Human CASP7-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 CASP7 in the samples is then calculated from the OD value by establishing a standard curve.

Cat no: ABQ-ES96-CASP7hu
ABQ-ES96-CASP7hu
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Human CASP7(Caspase 7) ELISA Kit

SKU

ABQ-ES96-CASP7hu

Applications

ELISA

Reactivity

Human

Alternative Name

CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3, Caspase 7

Standard

20ng/mL

Sensitivity

0.19 ng/mL

Detection Range

0.32-20ng/mL.

Sample Type

Serum, Plasma, Tissue homogenate Cell culture supernatant and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Human CASP7(Caspase 7) ELISA Kit

Quanticon™ Human CASP7(Caspase 7) ELISA Kit

Quanticon™ Human CASP7(Caspase 7) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)
Principle of the ProcedureThis kit uses the Sandwich-ELISA principle. The microtiter plate strips has been pre-coated with an affinity purified antibody to Human CASP7. Standards or samples containing Human CASP7 are added to the plate and reacted with capture antibody. A second anti-Human CASP7 antibody labeled biotin is then added and binds to Human CASP7 captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Human CASP7-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 CASP7 in the samples is then calculated from the OD value by establishing a standard curve. Cat no: ABQ-ES96-CASP7hu ABQ-ES96-CASP7hu Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ Human CASP7(Caspase 7) ELISA Kit
SKUABQ-ES96-CASP7hu
ApplicationsELISA
ReactivityHuman
Alternative Name CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3, Caspase 7
Standard 20ng/mL
Sensitivity0.19 ng/mL
Detection Range0.32-20ng/mL.
Sample TypeSerum, Plasma, Tissue homogenate Cell culture supernatant and Other biological samples
Sample Volume100 ÎĽL
Assay TypeSandwich
Assay Duration3.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ Human CASP7(Caspase 7) ELISA Kit
SKUABQ-ES96-CASP7hu
ApplicationsELISA
ReactivityHuman
Alternative Name CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3, Caspase 7
Standard 20ng/mL
Sensitivity0.19 ng/mL
Detection Range0.32-20ng/mL.
Sample TypeSerum, Plasma, Tissue homogenate Cell culture supernatant and Other biological samples
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