FGF-13 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES5243
Catalog Number: ELK-ES5243
Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
fibroblast growth factor 13(FGF13) Homo sapiens 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. [provided by RefSeq, Nov 2008],
Alternative Names:
FGF13, FHF2, Fibroblast growth factor 13, FGF-13, Fibroblast growth factor homologous factor 2, FHF-2
Immunogen: The antiserum was produced against synthesized peptide derived from human FGF13. AA range:154-203
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 28
GeneID: FGF13
Storage: -20°C/1 year
NOTE: For Research Use Only
fibroblast growth factor 13(FGF13) Homo sapiens 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. [provided by RefSeq, Nov 2008],
Alternative Names:
FGF13, FHF2, Fibroblast growth factor 13, FGF-13, Fibroblast growth factor homologous factor 2, FHF-2
Immunogen: The antiserum was produced against synthesized peptide derived from human FGF13. AA range:154-203
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 28
GeneID: FGF13
Storage: -20°C/1 year
NOTE: For Research Use Only
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