Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

Principle of the Procedure

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with rT3. During the reaction, rT3 in the sample or standard competes with a fixed amount of rT3 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to rT3. 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 rT3 in tested samples can be calculated by comparing the OD of the samples to the standard curve

Cat no: ABQ-EC96-RT3ge
ABQ-EC96-RT3ge
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

SKU

ABQ-EC96-RT3ge

Applications

ELISA

Reactivity

General/Universal

Alternative Name

RT3, r-T3, and Reverse T3

Standard

6000 pg/mL

Sensitivity

27.55 pg/mL

Detection Range

93.75-6000 pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell Lysates 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™ rT3(Reverse Triiodothyronine) ELISA Kit

Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)

Principle of the Procedure

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with rT3. During the reaction, rT3 in the sample or standard competes with a fixed amount of rT3 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to rT3. 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 rT3 in tested samples can be calculated by comparing the OD of the samples to the standard curve

Cat no: ABQ-EC96-RT3ge ABQ-EC96-RT3ge Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ rT3(Reverse Triiodothyronine) ELISA Kit

SKU

ABQ-EC96-RT3ge

Applications

ELISA

Reactivity

General/Universal

Alternative Name

RT3, r-T3, and Reverse T3

Standard

6000 pg/mL

Sensitivity

27.55 pg/mL

Detection Range

93.75-6000 pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell Lysates 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™ rT3(Reverse Triiodothyronine) ELISA Kit

SKU

ABQ-EC96-RT3ge

Applications

ELISA

Reactivity

General/Universal

Alternative Name

RT3, r-T3, and Reverse T3

Standard

6000 pg/mL

Sensitivity

27.55 pg/mL

Detection Range

93.75-6000 pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell Lysates 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