Recombinant Human FGFR2 (N-GST tag) | Z500142

abm | Recombinant Human FGFR2 (N-GST tag) | Z500142

FGFR2 is a member of the fibroblast growth factor receptor family which play a role in mitogenesis and differentiation. FGFR2 is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, and mutations in FGFR2 are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis . FGFR2 is required for early postimplantation development between implantation and the formation of the egg cylinder . FGFR2 contributes to the outgrowth, differentiation, and maintenance of the inner cell mass.

Functions:

The specific activity of FGFR2 was determined to be 118 nmol /min/mgas per activity assay protocol.

Organism:

Human

Source:

Insect cells

Alias:

K-SAM, BFR-1, CEK3, ECT1, TK14, TK25, CD332, JWS, TK14

Gene Symbol:

FGFR2

Gene ID:

N/A

Accession:

BC039243

Formulation:

50mM Tris-HCl, pH 7.5, 150mM NaCl, 10mM glutathione, 0.1mM EDTA, 0.25mM DTT, 0.1mM PMSF, 25% glycerol.

Solubility:

N/A

Appearance:

Liquid

Molecular Weight (kDa):

72

Molecular Weight 2 (kDA):

N/A

Molecular Weight 3 (kDA):

N/A

Purity:

70% - 90%

Concentration:

Shipping Condition :

Dry Ice

Storage Condition:

Store product at –70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.