tcue245 ELISA Kit for Gastric Inhibitory Polypeptide (GIP)

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Data sheet

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Test Principle

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Gastric Inhibitory Polypeptide (GIP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Gastric Inhibitory Polypeptide (GIP) and unlabeled Gastric Inhibitory Polypeptide (GIP) (Standards or samples) with the pre-coated antibody specific to Gastric Inhibitory Polypeptide (GIP). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Gastric Inhibitory Polypeptide (GIP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Gastric Inhibitory Polypeptide (GIP) in the sample.

Information

Research AreaEndocrinology
Gastroenterology
Hormone metabolism
Species ReactivityMus musculus (Mouse)
Sample TypeSerum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Specifications

Tested ApplicationELISA
SensitivityThe minimum detectable dose of this kit is typically less than 25.2pg/mL
Detection Range61.7-5,000pg/mL
Assay Time2h
Detection MethodEnzyme-linked immunosorbent assay for Antigen Detection.

Misc Information

SwissProtP48756
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