Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

Principle of the Procedure

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre coated with an antibody specific to Human PGII, and the Human PGII standard plate wells that pre coated using protein related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP conjugated antibody specific to Human PGII . After TMB substrate solution is added, only those wells that contain Human PGII and HRP conjugated antibody will exhibit a change in color. 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 PGII in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-ZS96-PGIIhu
ABQK-ZS96-PGIIhu
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

SKU

ABQK-ZS96-PGIIhu

Applications

ELISA

Reactivity

Human

Alternative Name

PGII

Standard

10 ng/mL

Sensitivity

7 pg/mL

Detection Range

0.16-10 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Sandwich

Assay Duration

1.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

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

Principle of the Procedure

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre coated with an antibody specific to Human PGII, and the Human PGII standard plate wells that pre coated using protein related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP conjugated antibody specific to Human PGII . After TMB substrate solution is added, only those wells that contain Human PGII and HRP conjugated antibody will exhibit a change in color. 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 PGII in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-ZS96-PGIIhu ABQK-ZS96-PGIIhu Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

SKU

ABQK-ZS96-PGIIhu

Applications

ELISA

Reactivity

Human

Alternative Name

PGII

Standard

10 ng/mL

Sensitivity

7 pg/mL

Detection Range

0.16-10 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Sandwich

Assay Duration

1.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Product Name

Quanticon™ XcelStep Human PGII(Pepsinogen II) ELISA Kit

SKU

ABQK-ZS96-PGIIhu

Applications

ELISA

Reactivity

Human

Alternative Name

PGII

Standard

10 ng/mL

Sensitivity

7 pg/mL

Detection Range

0.16-10 ng/mL

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

50 ÎĽL

Assay Type

Sandwich

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