Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

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

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

Product name

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

SKU

ABQ-EC96-NPYrt

Applications

ELISA

Reactivity

RAT

Sensitivity

0.39 pg/mL.

Detection Range

1.56-100pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

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

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

Product name

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

SKU

ABQ-EC96-NPYrt

Applications

ELISA

Reactivity

RAT

Sensitivity

0.39 pg/mL.

Detection Range

1.56-100pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations

Product name

Quanticon™ Rat NPY(Neuropeptide Y) ELISA Kit

SKU

ABQ-EC96-NPYrt

Applications

ELISA

Reactivity

RAT

Sensitivity

0.39 pg/mL.

Detection Range

1.56-100pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

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