FGF13 (NM_004114) Human 3' UTR Clone

CAT#: SC213833

3' UTR clone of fibroblast growth factor 13 (FGF13) transcript variant 1 for miRNA target validation

Specifications

Product Data

• Vector: pMirTarget
• Species: Human
• Transfection Reporter: RFP
• Assay Reporter: Luciferase
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Symbol: FGF13
• Synonyms: DEE90; FGF-13; FGF2; FHF-2; FHF2; LINC00889
• ACCN: NM_004114
• Insert Size: 2000 bp
• Sequence Data:
  Insert Sequence

  >SC213833 3’UTR clone of NM_004114
  The sequence shown below is from the reference sequence of NM_004114. The complete sequence of this clone may contain minor differences, such as SNPs.
  Blue=Stop Codon Red=Cloning site
  
  GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
  TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
  AAATCCATGAGCCACAATGAATCAACGTAGCCAGTGAGGGCAAAAGAAGGGCTCTGTAACAGAACCTTA
  CCTCCAGGTGCTGTTGAATTCTTCTAGCAGTCCTTCACCCAAAAGTTCAAATTTGTCAGTGACATTTAC
  CAAACAAACAGGCAGAGTTCACTATTCTATCTGCCATTAGACCTTCTTATCATCCATACTAAAGCCCCA
  TTATTTAGATTGAGCTTGTGCATAAGAATGCCAAGCATTTTAGTGAACTAAATCTGAGAGAAGGACTGC
  CAAATTTTCTCATGATCTCACCTATACTTTGGGGATGATAATCCAAAAGTATTTCACAGCACTAATGCT
  GATCAAAATTTGCTCTCCCACCAAGAAAATGTAAAAGACCACAATTGTTCTTCAAAAACAAACAAAACA
  AAACAAAACAAAATTAACTGCTTAAATGTTTTGTCGGGGCAAACAAAATTATGTGAATTGTGTTGTTTT
  CTTGGCTTGATGTTTTCTATCTACGCTTGATTCACATGTACTCTTTTCTTTGGCATAGTGCAACTTTAT
  GATTTCTGAAATTCAATGGTTCTATTGACTTTTTGCGTCACTTAATCCAAATCAACCAAATTCAGGGTT
  GAATCTGAATTGGCTTCTCAGGCTCAAGGTAACAGTGTTCTTGTGGTTTGACCAATTGTTTTTCTTTCT
  TTTTTTTTTTTTTTAGATTTGTGGTATTCTGGTCAAGTTATTGTGCTGTACTTTGTGCGTAGAAATTGA
  GTTGTATTGTCAACCCCAGTCAGTAAAGAGAACTTCAAAAAATTATCCTCAAGTGTAGATTTCTCTTAA
  TTCCATTTGTGTATCATGTTAAACTATTGTTGTGGCTTCTTGTGTAAAGACAGGAACTGTGGAACTGTG
  ATGTTGTCTTTTGTGTTGTTAAAATAAGAAATGTCTTATCTGTATATGTATGAGTCTTCCTGTCATTGT
  ATTTGGCACATGAATATTGTGTACAAGGAATTGTTAAGACTGGTTTTCCCTCAACAACATATATTATAC
  TTGCTACTGGAAAAGTGTTTAAGACTTAGCTAGGTTTCCATTTAGATCTTCATATCTGTTGCATGGAAG
  AAAGTTGGGTTCTTGGCATAGAGTTGCATGATATGTAAGATTTTGTGCATTCATAATTGTTAAAAATCT
  GTGTTCCAAAAGTGGACATAGCATGTACAGGCAGTTTTCTGTCCTGTGCACAAAAAGTTTAAAAAAGTT
  GTTTAATATTTGTTGTTGTATACCCAAATACGCACCGAATAAACTCTTTATATTCATTCAAAGAATAAT
  CTTCCAACATGTATTTATTGAGCGTCCATTATGTGCCAGTAACTGAAGTAGCAACTGGAAGTAAACATT
  GTATAATGCAGATAAGGTCACTGTCCTCAGATAGTCTACAGTCTAGAGAGTCATATTAACATGAACACT
  TTAAAGTGTGTTTATTTTACTAGTTACTGTACTTGCACTTCAGATTGGTACAAAGGAATTCACATTCCC
  GTTCAGTAGTCAAATTATACAAATGAGGCGTTTGTGCTAGTATTTTCTCTGCCACTCACAGTGTCATTT
  CCCCTCTCTGTTGCTTATTTCTCTCCTCTCTAGAGGGAATACACAGGACTAAATAGTGTCCTTTCTACC
  TTTGAGAACTGAAGGAAAATGTAAATTTTTTTAAATGTTGATGACTTTTCTCTAGCTCCCCAAAGCTGC
  ATTGTCTGGCAATGAACACTTTGAGAACAGTCAATACAGATGGTCTCTGACTTACAGTAGTTCAACTTA
  CATTTTTTCGGGGGCTTTACAGTGGTACAGAAGCAATAGGCATTTAGTAGAACTCATACTTTACCATAC
  AACCATTTTGCTTTTTATTTCCAGTACACTATTCAATAAATGACATGAGCTATTCAACACTTTTTAATT
  ACAAAATTTGCTTTGTAGTACATGATTTTGTCCAACTGTAAGCTAATATAAGCGTTCTAAGCACATTT
  ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA
  CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
  
• Restriction Sites: SgfI-MluI
• OTI Disclaimer: Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
• Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials.

Reference Data

• RefSeq: NM_004114.5
• Summary: The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]
• Locus ID: 2258
• MW: 77.2