Catalog: | C-EL-2005T |
Product Type: | Test kit |
Size: | 96 tests |
Principle: | Sandwich ELISA |
Species: | Human |
Detection range: | 0.313-20 ng/mL |
Sensitivity: | 0.03 ng/mL |
Sample type: | Serum, Plasma, Cell culture supernatants |
Test type: | Quantitative |
Analysis mode: | ELISA |
Storage: | All the reagents are stored at 2-8℃. Refer to the protocol for further storage instructions. |
Synonyms:: | BN, gastrin releasing peptide, GRP, GRP 10, preproGRP, proGRP |
Application: | Glycoprotein 130 (gp130, also known as IL6ST, CD130 or IL6-beta) is a ubiquitously expressed, signal-transducing receptor that serves as the signal transduction unit for IL-6 family of cytokines, including IL-6, IL-11, IL-27, leukemia inhibitory factor (LIF), OSM, ciliary neurotrophic factor (CNTF), cardiotrophin 1 (CT-1), and cardiotrophin-like cytokine (CLC). These cytokines signal through the gp130/Jak/STAT pathway. Binding of IL-6 to IL-6R induces gp130 homodimerization and formation of a high-affinity receptor complex, which activates Jaks. That causes phosphorylation of gp130 tyrosine residues which in turn activates STAT3. gp130 is a type I transmembrane protein, and can also exist as a soluble form (sgp130). sgp130 binds to sIL-6R/IL-6 complexes and prevents their interactions with membrane-anchored gp130 on target cells. |
This test kit is a solid phase sandwich Enzyme Linked-Immuno-Sorbent Assay (Sandwich ELISA). The GRP ELISA kit is to be used to detect and quantify protein levels of endogenous GRP. The assay recognizes human GRP. An antibody specific for GRP has been pre-coated onto the microwells. The GRP protein in samples is captured by the coated antibody after incubation. Following extensive washing, another antibody specific for GRP is added to detect the captured GRP protein. For signal development, horseradish peroxidase (HRP)-conjugated antibody is added, followed by Tetramethyl-benzidine (TMB) reagent. Solution containing sulfuric acid is used to stop color development and the color intensity which is proportional to the quantity of bound protein is measurable at 450nm with the correction wavelength set at 630 nm.
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