Recombinant Mouse Hgf protein (His Tag)

Species

Mouse

Purity

>90 %, SDS-PAGE

Tag

His Tag

Activity

not tested

Cat no : Eg0675



Product Information

Purity >90 %, SDS-PAGE
Endotoxin <0.1 EU/μg protein, LAL method
Activity
Not tested
Expression CHO-derived Mouse Hgf protein Gln33-Leu728 (Accession# Q08048-1) with a His tag at the C-terminus.
GeneID 15234
Accession Q08048-1
PredictedSize 80.4 kDa
SDS-PAGE 28 kDa, 50-55kDa and 72-85 kDa, reducing (R) conditions
Formulation Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
Reconstitution Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
Storage Conditions
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

Background

Hepatocyte growth factor (HGF) is the most potent mitogen of mature hepatocytes in primary culture. HGF is derived from a biologically inactive single-chain precursor of 728 amino acids (pro-HGF) localized mostly on the cell surface and in the extracellular matrix. The mature form produced following proteolytic cleavage is composed of a 69-kDa alpha-subunit (containing four kringle domains) and the 34 kDa beta-subunit, similar to the catalytic domain of serine proteases, but with amino acid substitutions in the active site. HGF is a pleiotropic cytokine that exerts a variety of effects on several cells, being involved in the regulation of many biological processes, such as inflammation, tissue repair, morphogenesis, angiogenesis, tumor propagation, immunomodulation of viral infections and cardio-metabolic activities

References:

1. Matsumoto K. et al.(1991). J Gastroenterol Hepatol. 6(5): 509-19. 2. Mizuno K. et al.(1993).EXS. 65:1-29. 3. Bardelli A. et al. (1994). J Biotechnol. 37(2):109-22. 4. Stuart KA. et al. (2000). Int J Exp Pathol. 81(1):17-30. 5. Libetta C. et al. (2016). Clin Exp Nephrol. 20(3):371-8.

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