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Rabbit Anti-FGF12 Antibody (CSB-PA008618ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Fibroblast growth factor 12 Antibody,FGF-12 Antibody,Fibroblast growth factor homologous factor 1 Antibody,FHF-1 Antibody,Myocyte-activating factor Antibody,FGF12 Antibody,FGF12B Antibody,FHF1 AntibodyMore alternative names for the antibody
FGF-12 antibody|Fgf12 antibody|FGF12_HUMAN antibody|FGF12B antibody|FHF-1 antibody|FHF1 antibody|Fibroblast growth factor 12 antibody|Fibroblast growth factor 12B antibody|Fibroblast growth factor FGF 12b antibody|Fibroblast growth factor homologous factor 1 antibody|Myocyte activating factor antibody|Myocyte-activating factor antibody
Anti-FGF12 antibody (ab125682)
Anti-FGF12 antibody (ab125682)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Fibroblast growth factor 12 protein (1-181AA)
|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:2257( Human), Entrez Gene:14167( Mouse), Entrez Gene:170630( Rat), Omim:601513( Human), SwissProt:P61328( Human), SwissProt:P61329( Mouse), SwissProt:P61150( Rat), Unigene:390250( Human), Unigene:7996( Mouse), Unigene:45965( Rat)
|Protein function|| |
Involved in nervous system development and function. Involved in the positive regulation of voltage-gated sodium channel activity. Promotes neuronal excitability by elevating the voltage dependence of neuronal sodium channel SCN8A fast inactivation. .
|Protein tissue specificity|| |
Brain, eye and testis; highly expressed in embryonic retina, olfactory epithelium, olfactory bulb, and in a segmental pattern of the body wall; in adult olfactory bulb, less in cerebellum, deep cerebellar nuclei, cortex and multiple midbrain structures.
|Involvement in disease|| |
Epileptic encephalopathy, early infantile, 47 (EIEE47) [MIM:617166]: A form of epileptic encephalopathy, a heterogeneous group of severe childhood onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. . 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 cellular localization|| |
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CUSABIO BIOTECH CO.
|Product type|| |
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