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Human Fibroblast Growth Factor Receptor 2 (FGFR2) ELISA Kit

Human Fibroblast Growth Factor Receptor 2 (FGFR2) ELISA Kit

This ELISA kit is designed to detect Human Fibroblast Growth Factor Receptor 2 (Human FGFR2). The assay plate has been pre-coated with mouse anti-Human FGFR2 monoclonal antibody. When the sample containing FGFR2 is added to the plate, it binds to the antibodies coated on the wells. Then, a horseradish peroxidase conjugated mouse anti-Human FGFR2 Antibody is added to the wells and binds to FGFR2 in the sample. After washing the wells, substrate solutions are added, and the color intensity is directly proportional to the amount of Human FGFR2 present. The reaction is stopped by adding an acidic stop solution, and the absorbance is measured at 450 nm.

Catalog No: BPE138
Regular price $754.00 USD
Regular price $580.00 USD Sale price $754.00 USD
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Product Details

Species Reactivity Human
Sensitivity 7.15 pg/mL
Detection Range 23.44-1500 pg/mL
Sample Type Serum, plasma, cell culture supernates
Incubation(s) 3.5 hour(s)
Research Areas Signal Transduction, Cancer, Cardiovascular, Developmental Biology, Neuroscience, Stem cells
Background 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. Cancer Immunotherapy Immune Checkpoint Immunotherapy Targeted Therapy
Shipping Condition Shipped on cold gel packs.
Storage Condition and Shelf Life This product can be stored at 2-8C.
Analyte Fibroblast growth factor receptor 2
Regulatory Status For Research Use Only
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