Quanticon™ E1(Estrone) ELISA Kit

Quanticon™ E1(Estrone) ELISA Kit

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with E1. During the reaction, E1 in the sample or standard competes with a fixed amount of E1 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to E1. 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 E1 in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-E1ge
ABQ-EC96-E1ge
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ E1(Estrone) ELISA Kit

SKU

ABQ-EC96-E1ge

Applications

ELISA

Reactivity

General/ Universal

Alternative Name

Oestrone

Standard

2000 pg/mL.

Sensitivity

8.86 pg/mL.

Detection Range

31.25-2000 pg/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™ E1(Estrone) ELISA Kit

Quanticon™ E1(Estrone) ELISA Kit

Quanticon™ E1(Estrone) 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 E1. During the reaction, E1 in the sample or standard competes with a fixed amount of E1 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to E1. 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 E1 in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-E1ge ABQ-EC96-E1ge Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ E1(Estrone) ELISA Kit

SKU

ABQ-EC96-E1ge

Applications

ELISA

Reactivity

General/ Universal

Alternative Name

Oestrone

Standard

2000 pg/mL.

Sensitivity

8.86 pg/mL.

Detection Range

31.25-2000 pg/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   

Product Name

Quanticon™ E1(Estrone) ELISA Kit

SKU

ABQ-EC96-E1ge

Applications

ELISA

Reactivity

General/ Universal

Alternative Name

Oestrone

Standard

2000 pg/mL.

Sensitivity

8.86 pg/mL.

Detection Range

31.25-2000 pg/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   

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