Quanticon™ XcelStep Rat ADP(Adiponectin) ELISA Kit

Quanticon™ XcelStep Rat ADP(Adiponectin) 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 ADP, and the Rat ADP standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat ADP . After TMB substrate solution is added, only those wells that contain Rat ADP and HRP-conjugated antibody 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 ADP in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-ZS96-ADPrt
ABQK-ZS96-ADPrt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ XcelStep Rat ADP(Adiponectin) ELISA

Kit

SKU

ABQK-ZS96-ADPrt

Applications

ELISA

Reactivity

Rat

Alternative Name

ApM1, AdipoQ, Acrp30

Standard

500 ng/mL

Sensitivity

4.75 ng/mL

Detection Range

7.82-500 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Feces, Cell culture supernatants and other biological fluids and Cerebrospinal fluid (CSF)

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ XcelStep Rat ADP(Adiponectin) ELISA Kit

Quanticon™ XcelStep Rat ADP(Adiponectin) ELISA Kit

Quanticon™ XcelStep Rat ADP(Adiponectin) 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 ADP, and the Rat ADP standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat ADP . After TMB substrate solution is added, only those wells that contain Rat ADP and HRP-conjugated antibody 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 ADP in the samples is then determined by comparing the OD of the samples to the standard curve. Cat no: ABQK-ZS96-ADPrt ABQK-ZS96-ADPrt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ XcelStep Rat ADP(Adiponectin) ELISAKit
SKUABQK-ZS96-ADPrt
ApplicationsELISA
ReactivityRat
Alternative Name ApM1, AdipoQ, Acrp30
Standard 500 ng/mL
Sensitivity4.75 ng/mL
Detection Range7.82-500 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, Feces, Cell culture supernatants and other biological fluids and Cerebrospinal fluid (CSF)
Sample Volume100 ÎĽL
Assay TypeSandwich
Assay Duration3.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ XcelStep Rat ADP(Adiponectin) ELISAKit
SKUABQK-ZS96-ADPrt
ApplicationsELISA
ReactivityRat
Alternative Name ApM1, AdipoQ, Acrp30
Standard 500 ng/mL
Sensitivity4.75 ng/mL
Detection Range7.82-500 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, Feces, Cell culture supernatants and other biological fluids and Cerebrospinal fluid (CSF)
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