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Read our guarantee »Products:Cardiovascular >> Angiogenesis >> Growth Factors >> FGF >> FGF
FGF9 protein
See all FGF9 products (5) ...
Highly pure (>98%) recombinant mouse FGF9.
E. coli
Sterile filtered Greater than 95% pure by SDS-PAGE and HPLC analyses. Endotoxin level is less than 0.1 ng per µg (1EU/µg).
Lyophilised:
Reconstitute using 50ul of sterile H20.
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
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Recombinan t Murine FGF-9 is a 23.3 kDa protein containing 205 amino acid residues: PLGEVGS YFG VQDAVPFGN V PVLPVDSP VL LNDHLGQ SEA GGLPRG PAVT DLDHL KGILRRRQLY CRTGF HLEI FPNGTI QGT RKDHSRF GI LEFISIAV G LVSIRGVDS GLYLGMNEKG ELYGSEKLTQ ECVFREQFE E NWYNTYSS NL YKHVDTG RRY YVALNK DGTP REGTR TKRHQKFTHF LPRPV DPDK VPELYK DIL SQS
Developmental Biology >> Reproduction >> Placental development
Developmental Biology >> Reproduction >> Sex determination
Neuroscience >> Neurology process >> Neuroregeneration >> Neuroregeneration
Neuroscience >> Neurology process >> Neurogenesis
Signal Transduction >> Growth Factors/Hormones >> FGF
Cardiovascular >> Angiogenesis >> Growth Factors >> FGF >> FGF
Our Abpromise guarantee covers the use of ab9745 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
FuncS: Use at an assay dependent dilution.
SDS-PAGE: Use at an assay dependent dilution.
This peptide can be used with studies using ab9743.
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.
Glial cells.
Defects in FGF9 are the cause of multiple synostoses syndrome type 3 (SYNS3) [MIM:612961]. Multiple synostoses syndrome is an autosomal dominant condition characterized by progressive joint fusions of the fingers, wrists, ankles and cervical spine, characteristic facies and progressive conductive deafness.
Belongs to the heparin-binding growth factors family.
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.
Secreted.
Target information above from: UniProt accessionP31371
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ab9745 has not yet been referenced specifically in any publications.
Publishing research using ab9745? Please let us know so that we can cite the reference in this datasheet
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