FGF13 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, tumour 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.
Antibodies
Application
Immunohistochemistry
Application Note
For research purposes only. Not for use in humans.
Dilution
1:2000 - 1:4000
Host
Rabbit Polyclonal
Immunogen
KLH conjugated Synthetic peptide corresponding to Mouse FGF13
Isotype
IgG
Positive Tissue
Striatum, Substantia Nigra
Purity
Affinity purification
Species
Mouse, Rat
Storage
Store at -20 ℃ for one year. Avoid repeated freeze/ thaw cycles.
