The protein FGFR1 is highly conserved between members and throughout evolution. This particular family member of FGFR1 binds both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations of FGFR1 protein have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, squamous cell lung cancer and autosomal dominant Kallmann syndrome.

推荐稀释比 ELISA:1/1000-1/2000;WB:1/500-1/1000;IHC-P:1/50-1/100

Western blot analysis of recombinant FGFR1(P252S) and wild type proteins.Purified His-tagged FGFR1(P252S) protein (22-376aa, 45KD, lane 2) and corresponding wild type protein (lane 1) were blotted with Anti-FGFR1(P252S) monoclonal antibody.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。