FGF13 polyclonal, anti-human, mouse, rat

Background:
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.

Synonyms: FGF-13, FGF2, FHF-2, FHF2

Cellular Location: Cell projection Cytoplasm Cytoplasm Nucleus dendrite filopodium growth cone nucleolus

Immunogen:
Recombinant protein of human FGF13

Gene Symbol: FGF13

Gene ID: 2258

Swiss prot: Q92913

Calculated MW: 28kDa

Recommended dilution:
WB 1:500-2000, IHC 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.