
英文名称:FGFR-3/CD333/FGFR3 (C-Fc), Human, Recombinant
货号:GPCK140
价格: ¥8280.00 ¥1180.00 ¥580.00 ¥11880.00
产品详情
500μg / 50μg / 10μg / 1mg
物种Human
表达宿主Human Cells
PHGlu23-Gly375
序列信息Glu23-Gly375
检索号P22607
分子量64.8 kDa
表观分子量95-110 kDa
生物活性Immobilized Human FGF-12 at 2 μg/mL (100 μL/well) can bind Human FGFR3-Fc. The ED50 of Recombinant Human FGFR3-Fc is 0.5-4 μg/mL.
纯度> 95% as determined by reducing SDS-PAGE.
内毒素< 0.1 EU/μg
制剂Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
复融Always centrifuge tubes before opening. Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100 μg/mL. Dissolve the lyophilized protein in sterile water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
储存条件Lyophilized protein should be stored at -5~-20℃, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at -5~-20℃ for 3 months.
运输条件Ambient temperature or ice pack.
有效期12个月
背景介绍Fibroblast Growth Factors (FGFs) are involved in a multitude of physiological and pathological cellular processes. The biological activities of the FGFs are mediated by a family of type I transmembrane tyrosine kinases which undergo dimerization and autophosphorylation after Ligand binding. Four distinct genes encoding closely related FGF Receptors, FGF R1-4, are known. All four genes for FGF Rs encode Proteins with an N-terminal signal peptide, three immunoglobulin (Ig)-like domains, an acid-box region containing a run of acidic residues between the IgI and IgII domains, a transmembrane domain and the split tyrosine-kinase domain. Multiple forms of FGF R1-3 are generated by alternative splicing of the mRNAs. A frequent splicing event involving FGF R1 and 2 results in Receptors containing all three Ig domains, referred to as the α isoform, or only IgII and IgIII, referred to as the β isoform. Only the α isoform has been identified for FGF R3 and FGF R4. Additional splicing events for FGF R1-3, involving the C-terminal half of the IgIII domain encoded by two mutually exclusive alternative exons, generate FGF Receptors with alternative IgIII domains (IIIb and IIIc). The complex patterns of expression of these Receptors as well as the specificity of their interactions with the various FGF Ligand family members are under investigation.