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Human BMP7 ELISA Kit

  • Product Information
  • Description
Catalog: C-EL-1951T
Product Type: Test kit
Size: 96 tests
Principle: Sandwich ELISA
Species: Human
Detection range: 15.6-1000 pg/mL
Sensitivity: 0.8 pg/mL
Sample type: Serum, Cell culture supernatants, Urine
Test type: Quantitative
Analysis mode: ELISA
Storage: All the reagents are stored at 2-8℃. Refer to the protocol for further storage instructions.
Synonyms:: BMP 7, BMP7, bone morphogenetic protein 7, Eptotermin alfa, OP 1, OP1, Osteogenic protein 1
Application: ATF4 is a transcription factor, that accumulates predominantly in osteoblasts, where it regulates terminal osteoblast differentiation and bone formation[PMID: 19016586]. As a basic leucine-zipper (bZip) transcription factor, ATF4 can regulate amino acid metabolism, cellular redox state, and anti-stress responses. It also regulates age-related and diet-induced obesity and glucose homeostasis in mammals, and has conserved metabolic functions in flies[PMID: 19726872]. Due to its location at chromosome 22q13, a region linked to schizophrenia, ATF4 is considered as a positional candidate gene for schizophrenia[PMID: 18163433]. Otherwise, since ATF4 is induced by tumour microenvironmental factors, and regulates processes relevant to cancer progression, it might serve as a potential therapeutic target in cancer.

This test kit is a solid phase sandwich Enzyme Linked-Immuno-Sorbent Assay (Sandwich ELISA). The BMP7 ELISA kit is to be used to detect and quantify protein levels of endogenous BMP7. The assay recognizes human BMP7. An antibody specific for BMP7 has been pre-coated onto the microwells. The BMP7 protein in samples is captured by the coated antibody after incubation. Following extensive washing, another antibody of biotinylated specific for human BMP7 is added to detect the captured human BMP7 protein. For signal development, Streptavidin-HRP 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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