Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

Principle

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with 17-OHP. During the reaction, 17-OHP in the sample or standard competes with a fixed amount of 17-OHP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to 17-OHP. 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 17-OHP in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-17OHPge
ABQ-EC96-17OHPge
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

SKU

ABQ-EC96-17OHPge

Applications

ELISA

Reactivity

General

Alternative Name

17-OHP, 17-Hydroxyprogesterone

Standard

2000pg/mL.

Sensitivity

87.3 pg/mL.

Detection Range

312.5-20000 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™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

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Untitled design (1)

Principle

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with 17-OHP. During the reaction, 17-OHP in the sample or standard competes with a fixed amount of 17-OHP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to 17-OHP. 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 17-OHP in tested samples can be calculated by comparing the OD of the samples to the standard curve.

Cat no: ABQ-EC96-17OHPge ABQ-EC96-17OHPge Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

SKU

ABQ-EC96-17OHPge

Applications

ELISA

Reactivity

General

Alternative Name

17-OHP, 17-Hydroxyprogesterone

Standard

2000pg/mL.

Sensitivity

87.3 pg/mL.

Detection Range

312.5-20000 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™ 17-OHP(17-Hydroxyprogesterone) ELISA Kit

SKU

ABQ-EC96-17OHPge

Applications

ELISA

Reactivity

General

Alternative Name

17-OHP, 17-Hydroxyprogesterone

Standard

2000pg/mL.

Sensitivity

87.3 pg/mL.

Detection Range

312.5-20000 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