Anti-FGF9 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-FGF9 Antibody (CSB-PA008638ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

FGF-9 Antibody,Glia-activating factor Antibody,GAF Antibody,Heparin-binding growth factor 9 Antibody,HBGF-9 Antibody,FGF9 Antibody

More 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)
Close sc-373716|sc-1368|sc-8413|sc-7876|sc-398730|sc-1369|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-FGF9 Antibody

Catalogue No.

CSB-PA008638ESR1HU

Reactivity

Human

Immunogen

Recombinant human FGF9 protein (1-208AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

23 kDa

Purification

Antigen Affinity Purified

Storage

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

Glial cells.

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

Secreted.

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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