Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat β-EP. During the reaction, Rat β-EP in the sample or standard competes with a fixed amount of Rat β-EP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Rat β-EP. 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 Rat β-EP in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-BEPrt
ABQ-EC96-BEPrt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

SKU

ABQ-EC96-BEPrt

Applications

ELISA

Reactivity

Rat

Alternative Name

β-EP, Beta-Endorphin

Standard

1000pg/mL

Sensitivity

9.38 pg/mL.

Detection Range

15.63-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 μL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Conditions

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

Quanticon™ Rat β-EP(Beta-Endorphin) 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 Rat β-EP. During the reaction, Rat β-EP in the sample or standard competes with a fixed amount of Rat β-EP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Rat β-EP. 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 Rat β-EP in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-BEPrt ABQ-EC96-BEPrt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

SKU

ABQ-EC96-BEPrt

Applications

ELISA

Reactivity

Rat

Alternative Name

β-EP, Beta-Endorphin

Standard

1000pg/mL

Sensitivity

9.38 pg/mL.

Detection Range

15.63-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 μL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Conditions

Product Name

Quanticon™ Rat β-EP(Beta-Endorphin) ELISA Kit

SKU

ABQ-EC96-BEPrt

Applications

ELISA

Reactivity

Rat

Alternative Name

β-EP, Beta-Endorphin

Standard

1000pg/mL

Sensitivity

9.38 pg/mL.

Detection Range

15.63-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Sample Volume

50 μL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Conditions

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