FGF23 Mouse Protein

CAT#: AR31140PU-S

FGF23 mouse recombinant protein, 5 µg

Specifications

Product Data

• Species: Mouse
• Expression Host: E. coli
• Expression cDNA Clone or AA Sequence:
  Protein Sequence

  MYPDTSPLLG SNWGSLTHLY TATARTSYHL QIHRDGHVDG TPHQTIYSAL MITSEDAGSV VITGAMTRRF LCMDLHGNIF GSLHFSPENC KFRQWTLENG YDVYLSQKHH YLVSLGRAKR IFQPGTNPPP FSQFLARRNE VPLLHFYTVR PRRHTRSAED PPERDPLNVL KPRPRATPVP VSCSRELPSA EEGGPAASDP LGVLRRGRGD ARGGAGGADR CRPFPRFV
• Predicted MW: 25.5 kDa
• Purity: >95% pure by SDS-PAGE and HPLC analyses
• Presentation: Purified
• Buffer: Presentation State: Purified
  State: Lyophilized (0.2μ Sterile filtered) purified protein
• Bioactivity: Biological: Determined by its ability to stimulate the proliferation of murine NIH-3T3 cells. The expected ED₅₀ for this effect is 0.3-0.5 μg/ml, in the presence of murine Klotho and heparin.
• Preparation: Lyophilized (0.2μ Sterile filtered) purified protein
• Protein Description: Recombinant murine FGF-23 is a 25.5 kDa globular protein containing 228 amino acid residues.
• Storage: Store lyophilized at 2-8°C for 6 months or at -20°C long term.
  After reconstitution store the antibody undiluted at 2-8°C for one month
  or (in aliquots) at -20°C long term.
  Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.

Reference Data

• RefSeq: NP_073148
• Locus ID: 64654
• UniProt ID: Q9EPC2, Q3U1V5
• Cytogenetics: 6 F3
• Synonyms: Fgf8b
• Summary: This gene encodes a member of the fibroblast growth factor family. The encoded protein regulates phosphate homeostasis and vitamin D metabolism. Mutation of the related gene in humans causes autosomal dominant hypophosphatemic rickets (ADHR). The secreted protein is further cleaved into N- and C-terminal chains, which results in loss of function. [provided by RefSeq, Mar 2013]