FGF10 Protein (AA 38-208)

N° du produit ABIN7274614

Cette protéine Recombinant FGF10 est exprimée dans Escherichia coli (E. coli).

Aperçu rapide pour FGF10 Protein (AA 38-208) (ABIN7274614)

Antigène: FGF10 (Fibroblast Growth Factor 10 (FGF10))

Type de proteíne: Recombinant

Origine: Humain

Source: Escherichia coli (E. coli)

Pureté: > 90 % as determined by Tris-Bis PAGE

Détail du produit

Attributs du protein: AA 38-208

Fonction: Human FGF10 Protein

Séquence: Gln38-Ser208

Attributs du produit: Recombinant Human FGF10 Protein is expressed from E.coli without tag.It contains Gln38-Ser208.

Stérilité: 0.22 μm filtered

niveau d'endotoxine: Less than 0.1 EU per μg by the LAL method.

Biological Activity Comment: The affinity constant of 0.299 nM as determined in SPR assay (Biacore T200). See testing image for detail.

Information d'application

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/mL is recommended. Dissolve the lyophilized protein in distilled water.

Buffer: Lyophilized from 0.22μm filtered solution in 20 mM Tris, 150 mM NaCl ( pH 8.0). Normally 8 % trehalose is added as protectant before lyophilization.

Stock: -20 °C,-80 °C

Stockage commentaire: -20 to -80°C for 12 months as supplied from date of receipt., -80°C for 3-6 months after reconstitution., 2-8°C for 2-7 days after reconstitution., Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles.

Date de péremption: 12 months

Détail du antigène

Antigène: FGF10 (Fibroblast Growth Factor 10 (FGF10))

Autre désignation: FGF10

Sujet: Fibroblast growth factor 10 (FGF10) regulates multiple stages of structural lung morphogenesis, cellular differentiation, and the response to injury. As a driver of lung airway branching morphogenesis, FGF10 signaling defects during development lead to neonatal lung disease. Lung diseases impact patients across the lifespan, from infants in the first minutes of life through the aged population. Congenital abnormalities of lung structure can cause lung disease at birth or make adults more susceptible to chronic disease.

Poids moléculaire: 19.3 kDa. The protein migrates to 25 kDa based on Tris-Bis PAGE result.

UniProt: O15520

Pathways: Signalisation RTK, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Stem Cell Maintenance, Tube Formation, Positive Regulation of Response to DNA Damage Stimulus