Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) 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 Human CLIP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CLIP. 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 Human CLIP in the samples is then determined by comparing the OD of the samples to the standard curve.

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

Product Name

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

SKU

ABQK-EC96-CLIPhu

Applications

ELISA

Reactivity

Human

Alternative Name

CLIP

Standard

1000 pg/mL

Sensitivity

4.94 pg/mL

Detection Range

15.63-1000 pg/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™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

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

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

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

Product Name

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

SKU

ABQK-EC96-CLIPhu

Applications

ELISA

Reactivity

Human

Alternative Name

CLIP

Standard

1000 pg/mL

Sensitivity

4.94 pg/mL

Detection Range

15.63-1000 pg/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   

Product Name

Quanticon™ Human CLIP(Corticotropin Like Intermediate Lobe Peptide) ELISA Kit

SKU

ABQK-EC96-CLIPhu

Applications

ELISA

Reactivity

Human

Alternative Name

CLIP

Standard

1000 pg/mL

Sensitivity

4.94 pg/mL

Detection Range

15.63-1000 pg/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   

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