Quanticon™ CNT(Carnitine) ELISA Kit

Quanticon™ CNT(Carnitine) ELISA Kit

Quanticon™ CNT(Carnitine) ELISA Kit

Quanticon™ CNT(Carnitine) ELISA Kit

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 CNT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to CNT. 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 CNT in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-EC96-CNTge
ABQK-EC96-CNTge
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ CNT(Carnitine) ELISA Kit

SKU

ABQK-EC96-CNTge

Applications

ELISA

Reactivity

General

Alternative Name

VB20, Vitamin B20

Standard

1000 ng/mL

Sensitivity

4.92 ng/mL

Detection Range

15.63-1000 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cell culture supernatant and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Competitive Inhibition

Assay Duration

1.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

Citations   

Quanticon™ CNT(Carnitine) ELISA Kit

Quanticon™ CNT(Carnitine) ELISA Kit

Quanticon™ CNT(Carnitine) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
Untitled design (1)
Principle of the ProcedureThis assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with CNT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to CNT. 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 CNT in the samples is then determined by comparing the OD of the samples to the standard curve. Cat no: ABQK-EC96-CNTge ABQK-EC96-CNTge Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA
Product Name Quanticon™ CNT(Carnitine) ELISA Kit
SKUABQK-EC96-CNTge
ApplicationsELISA
ReactivityGeneral
Alternative Name VB20, Vitamin B20
Standard 1000 ng/mL
Sensitivity4.92 ng/mL
Detection Range15.63-1000 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, Cell culture supernatant and Other biological samples
Sample Volume50 ÎĽL
Assay TypeCompetitive Inhibition
Assay Duration1.5 H
Detection Wavelength450nm
Storage2-8oC/-20 oC
Citations
Product Name Quanticon™ CNT(Carnitine) ELISA Kit
SKUABQK-EC96-CNTge
ApplicationsELISA
ReactivityGeneral
Alternative Name VB20, Vitamin B20
Standard 1000 ng/mL
Sensitivity4.92 ng/mL
Detection Range15.63-1000 ng/mL
Sample TypeSerum, Plasma, Tissue homogenate, Urine, Saliva, Cell culture supernatant and Other biological samples
Sample Volume50 ÎĽL
Assay TypeCompetitive Inhibition
Assay Duration1.5 H
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