Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

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 Rat MDA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MDA. 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 Rat MDA in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-EC96-MDArt
ABQK-EC96-MDArt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

SKU

ABQK-EC96-MDArt

Applications

ELISA

Reactivity

Rat

Alternative Name

MDA

Standard

2000pg/mL

Sensitivity

9.13 ng/mL

Detection Range

31.25-2000 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva and Cell culture supernatants and other biological fluids

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

2.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit

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Untitled design (1)
Principle of the ProcedureThis assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat MDA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MDA. 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 Rat MDA in the samples is then determined by comparing the OD of the samples to the standard curve. Cat no: ABQK-EC96-MDArt ABQK-EC96-MDArt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit
SKUABQK-EC96-MDArt
ApplicationsELISA
ReactivityRat
Alternative Name MDA
Standard 2000pg/mL
Sensitivity9.13 ng/mL
Detection Range31.25-2000 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva and Cell culture supernatants and other biological fluids
Sample Volume50 ÎĽL
Assay TypeCompetitive
Assay Duration2.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ Rat MDA(Malondialdehyde) ELISA Kit
SKUABQK-EC96-MDArt
ApplicationsELISA
ReactivityRat
Alternative Name MDA
Standard 2000pg/mL
Sensitivity9.13 ng/mL
Detection Range31.25-2000 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva and Cell culture supernatants and other biological fluids
Sample Volume50 ÎĽL
Assay TypeCompetitive
Assay Duration2.5 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