C14orf151 (INF2) (NM_032714) Human 3' UTR Clone

CAT#: SC210644

3`UTR clone of inverted formin FH2 and WH2 domain containing (INF2) transcript variant 3 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: INF2
• Synonyms: C14orf151; C14orf173; CMTDIE; FSGS5; pp9484
• ACCN: NM_032714
• Insert Size: 849
• Sequence Data:
  Insert Sequence

  >SC210644 3'UTR clone of NM_032714
  The sequence shown below is from the reference sequence of NM_032714. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  TGGCTCGCCTGCGGTGAGTCCCCACTGTAGCGGTCCTGCCGGCTCCCCCTCCTGCTCCCAAGGCCAGGCC
  CACCTGCCCTTTGGCTCCCAGCCACCTCACCTAAGCAGCACCTCCAGATGGCAGGGAGGTGGCTCCCTCG
  GAGTAACCCCAGGGGTCCAGCCAGAAGCCAGGTCTCAGGCTAGAATCCAGCTCACTGTCCCTGGCAGCTG
  CCCACAGAAACTAGGGTTGCAGCAGCCATAGAAAGGACAGAATGAGCTCATATCCTTTGCACACCGTGGA
  TGGAGCTGGAGGCCGTGATCCTAAGTGAACCAACCCAGAAACAGAAAATGAAATGCCAATAAGAGGGAAC
  TACAGGGTGGTTCACGTGGACGCAAGATGGAGACAGGGACACGGGCTCCAGGGCGAGAGTTGAAAAACTA
  CCTACAGGGTACAGTGTTCGTCGCTACTTGGTGTCAGGCCCACTAGAACAAGGGTCCCCAACCGCCAGGC
  TGCGGACCGGTACCTGGCCTATTGGAACCGGGCCACGCAGCAGGAAGTGAGCGGTGGGCGGGCATTCCTG
  CCTGAGCTGCACCTCATGTCAGATCAGCACTGCATTAGATTCTCCAGCGCACGCACGCGCGCAAGGGATC
  CAGGCTGCGCGCTCCTCATGACAATCTAATGCCTGATGATCGGGGGTGGAACAGTTTTATCCCTAAACCA
  TTCCCGTCACCCCAGTCTATGGAAAAATTGTCTTCCACAAAACCAGTCCCTGGTGCCAAAAAGGCTGGGG
  ACCACTGCCCTAGAAGGCAAATCGCCTACGTTACACAGTGTACCATGTGGCAAACACGCACATGTACCCC
  CGAGTCTAA
  
  ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
• 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).

Reference Data

• RefSeq: NM_032714.1
• Summary: This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5. [provided by RefSeq, Aug 2010]
• Locus ID: 64423