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Rabbit Anti-FGF9 Antibody (CSB-PA008638ESR1HU)
Supplier: CUSABIO BIOTECH CO.
FGF-9 Antibody,Glia-activating factor Antibody,GAF Antibody,Heparin-binding growth factor 9 Antibody,HBGF-9 Antibody,FGF9 AntibodyMore alternative names for the antibody
FGF 9 antibody|FGF-9 antibody|FGF9 antibody|FGF9_HUMAN antibody|Fibroblast growth factor 9 antibody|GAF (Glia-activafibroblast growth factor 9 (glia-activating factor) antibody|GAF antibody|Glia Activating Factor antibody|Glia-activating factor antibody|HBFG 9 antibody|HBFG9 antibody|HBGF-9 antibody|Heparin-binding growth factor 9 antibody|MGC119914 antibody|MGC119915 antibody|SYNS3 antibody
Anti-FGF9 antibody (ab71395)
Anti-FGF9 antibody (ab71395)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human FGF9 protein (1-208AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:2254( Human), Entrez Gene:14180( Mouse), Entrez Gene:25444( Rat), Entrez Gene:378562( Xenopus laevis), Omim:600921( Human), SwissProt:P31371( Human), SwissProt:P54130( Mouse), SwissProt:P36364( Rat), SwissProt:Q91875( Xenopus laevis), Unigene:111( Human), Unigene:8846( Mouse), Unigene:25174( Rat), Unigene:367( Xenopus laevis)
|Protein function|| |
Plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration. May have a role in glial cell growth and differentiation during development, gliosis during repair and regeneration of brain tissue after damage, differentiation and survival of neuronal cells, and growth stimulation of glial tumors. .
|Protein tissue specificity|| |
|Involvement in disease|| |
Multiple synostoses syndrome 3 (SYNS3) [MIM:612961]: A bone disease characterized by multiple progressive joint fusions that commonly involve proximal interphalangeal, tarsal-carpal, humeroradial and cervical spine joints. Additional features can include progressive conductive deafness and facial dysmorphism. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the heparin-binding growth factors family.
|Protein post-translational modifications|| |
Three molecular species were found (30 kDa, 29 kDa and 25 kDa), cleaved at Leu-4, Val-13 and Ser-34 respectively. The smaller ones might be products of proteolytic digestion. Furthermore, there may be a functional signal sequence in the 30 kDa species which is uncleavable in the secretion step.; N-glycosylated.
|Protein cellular localization|| |
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|Product type|| |
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