Fgf23 (NM_022657) Mouse Untagged Clone

CAT#: MC210228

Fgf23 (untagged) - Mouse fibroblast growth factor 23 (Fgf23), (10ug)

Specifications

Product Data

• Type: Mouse Untagged Clone
• Tag: Tag Free
• Symbol: Fgf23
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >MC210228 representing NM_022657
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGCTAGGGACCTGCCTTAGACTCCTGGTGGGCGCGCTCTGCACTGTCTGCAGCTTGGGCACTGCTAGAG
  CCTATCCAGACACTTCCCCATTGCTTGGCTCCAACTGGGGAAGCCTGACCCACCTGTACACGGCTACAGC
  CAGGACCAGCTATCACCTACAGATCCATAGGGATGGTCATGTAGATGGCACCCCCCATCAGACCATCTAC
  AGTGCCCTGATGATTACATCAGAGGACGCCGGCTCTGTGGTGATAACAGGAGCCATGACTCGAAGGTTCC
  TTTGTATGGATCTCCACGGCAACATTTTTGGATCGCTTCACTTCAACCCAGAGAATTGCAAGTTCCGCCA
  GTGGACGCTGGAGAATGGCTATGACGTCTACTTGTCGCAGAAGCATCACTACCTGGTGAGCCTGGGCCGC
  GCCAAGCGCATCTTCCAGCCGGGCACCAACCCGCCGCCCTTCTCCCAGTTCCTGGCGCGCAGGAACGAGG
  TCCCGCTGCTGCACTTCTACACTGTTCGCCCACGGCGCCACACGCGCAGCGCCGAGGACCCACCCGAGCG
  CGACCCACTGAACGTGCTCAAGCCGCGGCCCCGCGCCACGCCTGTGCCTGTATCCTGCTCTCGCGAGCTG
  CCGAGCGCAGAGGAAGGTGGCCCCGCAGCCAGCGATCCTCTGGGGGTGCTGCGCAGAGGCCGTGGAGATG
  CTCGCGGGGGCGCGGGAGGCGCGGATAGGTGTCGCCCCTTTCCCAGGTTCGTCTAG
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_022657
• ORF Size: 756 bp
• Insert Size: 756
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).

Reference Data

• RefSeq: NM_022657.4, NP_073148.1
• RefSeq Size: 2702
• RefSeq ORF: 756
• Locus ID: 64654
• Gene 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]