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FGF10 Protein (AA 38-208) (Biotin)

Recombinant FGF10 protein expressed in Escherichia coli (E. coli).
Catalog No. ABIN7274615

Quick Overview for FGF10 Protein (AA 38-208) (Biotin) (ABIN7274615)

Target

See all FGF10 Proteins
FGF10 (Fibroblast Growth Factor 10 (FGF10))

Protein Type

Recombinant

Origin

  • 10
  • 5
  • 4
Human

Source

  • 16
  • 2
  • 1
Escherichia coli (E. coli)

Purity

> 90 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
  • Protein Characteristics

    AA 38-208

    Purification tag / Conjugate

    This FGF10 protein is labelled with Biotin.

    Purpose

    Biotinylated Human FGF10 Protein (Primary Amine Labeling)

    Sequence

    Gln38-Ser208

    Characteristics

    Recombinant Biotinylated Human FGF10 Protein (Primary Amine Labeling) is expressed from E.coli without tag.It contains Gln38-Ser208.

    Sterility

    0.22 μm filtered

    Endotoxin Level

    Less than 1EU per μg by the LAL method.

    Biological Activity Comment

    The affinity constant of 147.70 nM as determined in SPR assay (Biacore T200). See testing image for detail.
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  • Restrictions

    For Research Use only
  • 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.

    Storage

    -20 °C,-80 °C

    Storage Comment

    -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.

    Expiry Date

    12 months
  • Target

    FGF10 (Fibroblast Growth Factor 10 (FGF10))

    Alternative Name

    FGF10

    Background

    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.

    Molecular Weight

    19.3 kDa same as Tris-Bis PAGE result.

    UniProt

    O15520

    Pathways

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