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FGFR2 ELISA Kit

  • Product Information
  • Description
Catalog: C-EL-1781T
Product Type: Test kit
Size: 96 tests
Principle: Solid Phase Sandwich ELISA
Conjugation: HRP
Species: Human
Detection range: 10.94-700 pg/mL
Sensitivity: 7.15 pg/mL
Specificity: Recognizes both recombinant and natural Human FGFR2
Interference: Preparations of FGF2、FGF6、FGF7、FGF9、FGF17、FGF21 and LYN at 12 ng/mL in a mid-range recombinant human CSTB control were assayed for interference. No significant interference was observed.
Sample type: Recombinant protein
Test type: Quantitative
Analysis mode: ELISA
Shipping: This ELISA Kit is shipped at ambient temperature.
Storage: 2-8℃
Full name: fibroblast growth factor receptor 2
Application: Receptor Tyrosine Kinases (RTKs); Cancer Drug Targets

This FGFR2 ELISA Kit, Human is an enzyme-linked immunosorbent assay for the quantitative measurement of Human FGFR2 protein in Recombinant protein . It contains recombinant Human FGFR2, and antibodies raised against the recombinant protein. This ELISA kit is complete and ready-to-use.FGFR2, also known as CD332, belongs to the fibroblast growth factor receptor subfamily where amino acid sequence is highly conserved between members and throughout evolution. FGFR2 acts as cell-surface receptor for fibroblast growth factors and plays an essential role in the regulation of cell proliferation, differentiation, migration and apoptosis, and in the regulation of embryonic development. It is required for normal embryonic patterning, trophoblast function, limb bud development, lung morphogenesis, osteogenesis and skin development. FGFR2 plays an essential role in the regulation of osteoblast differentiation, proliferation and apoptosis, and is required for normal skeleton development. It also promotes cell proliferation in keratinocytes and imature osteoblasts, but promotes apoptosis in differentiated osteoblasts. FGFR2 signaling is down-regulated by ubiquitination, internalization and degradation. Mutations that lead to constitutive kinase activation or impair normal CD332 maturation, internalization and degradation lead to aberrant signaling. Over-expressed FGFR2 promotes activation of STAT1. Defects in CD3322 are the cause of Crouzon syndrome, Jackson-Weiss syndrome, Apert syndrome, Pfeiffer syndrome, Beare-Stevenson cutis gyrata syndrome, familial scaphocephaly syndrome, lacrimo-auriculo-dento-digital syndrome and Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis.

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