The Human SST (Somatostatin) ELISA Kit is a reliable and accurate tool for detecting levels of somatostatin in human samples such as serum, plasma, and cell culture supernatants. With high sensitivity and specificity, this kit provides consistent and reproducible results, making it suitable for a variety of research applications.Somatostatin is a key hormone that regulates various physiological functions, including inhibiting the release of growth hormone, insulin, and glucagon. It also plays a role in modulating neurotransmission and cell proliferation. Dysregulation of somatostatin levels has been associated with several disorders, such as growth hormone disorders, diabetes, and certain tumors.This ELISA kit offers researchers a valuable tool for studying the role of somatostatin in health and disease, allowing for the development of potential diagnostic and therapeutic strategies. Discover more about the Human SST ELISA Kit at www.assaygenie.com.
Product Name:
Human SST (Somatostatin) ELISA Kit
SKU:
HUES02869
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Competitive
Assay type:
Competitive-ELISA
Assay time:
2 h 30 min
Sensitivity:
4.69 pg/mL
Detection range:
7.81-500 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with the target antigen. Standards or samples are added along with a biotinylated detection antibody. The target antigen present in the sample competes with the immobilized antigen for binding to the detection antibody. After incubation, Avidin-Horseradish Peroxidase (HRP) conjugate is added. Free components are washed away. The substrate solution is then added, resulting in a color change. The intensity of the color is inversely proportional to the concentration of the target antigen in the sample. The reaction is stopped by the addition of stop solution, and the color changes from blue to yellow. The optical density (OD) is measured at 450 nm ± 2 nm. The concentration of the target protein is calculated by comparing the OD values of the samples to the standard curve.
