FGFR3 Rabbit pAb
Cat No.: APA3526
Size:
Product Name: | FGFR3 Rabbit pAb |
Cat No.: | APA3526 |
source: | Rabbit |
reactivity: | Human |
applications: | WB,IHC,ICC/IF,FC |
clonality: | Polyclonal |
recommended dilution: | WB: 1:2000 IHC: 1:50 ICC/IF: 1:100 FC: 1:20 |
format: | Liquid |
isotype: | IgG |
immunogen: | A synthetic peptide of human FGFR3 |
calculated molecular weight: | 88 kDa |
observed molecular weight: | 125 kDa |
genbank accession number: | P22607 |
gene id (ncbi): | 2261 |
purification method: | Affinity Purification |
conjugate: | Un-conjugated |
storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt. |
synonyms: | ACH; CEK2; JTK4; CD333; HSFGFR3EX |
category: | Primary Ab |
concentration: | 0.5mg/ml |
background: | This gene encodes a member of the fibroblast growth factor receptor (FGFR) family, with its amino acid sequence being highly conserved between members and among divergent species. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds acidic and basic fibroblast growth hormone and plays a role in bone development and maintenance. Mutations in this gene lead to craniosynostosis and multiple types of skeletal dysplasia. [provided by RefSeq, Aug 2017] |