Human GIP (Gastric Inhibitory Polypeptide) ELISA Kit
The Human GIP (Gastric Inhibitory Polypeptide) ELISA Kit is specifically designed for the precise measurement of GIP levels in human serum, plasma, and cell culture supernatants. With its exceptional sensitivity and specificity, this kit ensures accurate and consistent results, making it an excellent choice for various research applications.Gastric Inhibitory Polypeptide, or GIP, is a vital hormone that regulates insulin secretion and plays a key role in glucose metabolism. Dysregulation of GIP levels has been implicated in metabolic disorders such as diabetes and obesity, making it a valuable biomarker for studying these conditions and potential therapeutic interventions.This ELISA kit provides researchers with a reliable tool to quantify GIP levels, furthering our understanding of its biological functions and clinical relevance. Invest in the Human GIP ELISA Kit for precise and reliable measurements of GIP levels in your research studies.
Product Name:
Human GIP (Gastric Inhibitory Polypeptide) ELISA Kit
SKU:
HUES02978
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
46.88 pg/mL
Detection range:
78.13-5000 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to the target protein. Standards or samples are added to the micro ELISA plate wells and bind to the immobilized antibody. A biotinylated detection antibody specific to the target protein is then added, followed by Avidin-Horseradish Peroxidase (HRP) conjugate. Free components are washed away. The substrate solution is added to each well, resulting in a color change. Only wells containing the target protein, detection antibody, and HRP conjugate will develop a blue color. The reaction is terminated by the addition of stop solution, resulting in a yellow color. The optical density (OD) is measured at 450 nm ± 2 nm. The OD value is directly proportional to the concentration of the target protein in the sample and is determined using a standard curve.
