Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Human 11,12-DHETs. During the reaction, Human 11,12-DHETs in the sample or standard competes with a fixed amount of Human 11,12-DHETs on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human 11,12-DHETs. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The concentration of Human 11,12-DHETs in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-11,12DHETShu
ABQ-EC96-11,12DHETShu
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

SKU

ABQ-EC96-11,12DHETShu

Applications

ELISA

Reactivity

Human

Alternative Name

11,12-DHETs

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

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

Citations   

Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Human 11,12-DHETs. During the reaction, Human 11,12-DHETs in the sample or standard competes with a fixed amount of Human 11,12-DHETs on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human 11,12-DHETs. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The concentration of Human 11,12-DHETs in tested samples can be calculated by comparing the OD of the samples to the standard curve. Cat no: ABQ-EC96-11,12DHETShu ABQ-EC96-11,12DHETShu Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit
SKUABQ-EC96-11,12DHETShu
ApplicationsELISA
ReactivityHuman
Alternative Name 11,12-DHETs
Standard 100ng/mL.
Sensitivity0.94 ng/mL.
Detection Range1.57-100ng/mL.
Sample TypeSerum, Plasma, Tissue homogenate and Other biological samples
Sample Volume50 ÎĽL
Assay TypeCompetitive
Assay Duration1.5H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ Human 11,12-DHETs(11,12-dihydroxyeicosatrienoic acids) ELISA Kit
SKUABQ-EC96-11,12DHETShu
ApplicationsELISA
ReactivityHuman
Alternative Name 11,12-DHETs
Standard 100ng/mL.
Sensitivity0.94 ng/mL.
Detection Range1.57-100ng/mL.
Sample TypeSerum, Plasma, Tissue homogenate and Other biological samples
Sample Volume50 ÎĽL
Assay TypeCompetitive
Assay Duration1.5H
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