PCDH15 (NM_001142766) Human 3' UTR Clone

CAT#: SC209613

3`UTR clone of protocadherin 15 (PCDH15) transcript variant E 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: PCDH15
• Synonyms: CDHR15; DFNB23; USH1F
• ACCN: NM_001142766
• Insert Size: 755
• Sequence Data:
  Insert Sequence

  >SC209613 3'UTR clone of NM_001142766
  The sequence shown below is from the reference sequence of NM_001142766. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  CTCACAGTCAATCTACTTCACTGTAATGTTGCTTTTCTTATTTTAGTCGGGCAAACCTCTTGTTGATCAT
  AGTCTTCAAGTTGAACATCAAATTTGAACGTCAAAGAAGACTCTATTATTTTACCCCAAATTCAATGAAA
  TGCAGTTTTTTTTCTCGTTTTTAATTTAAAAAGATATTAACCTCATCACTACTAACTCACTCATATAATA
  GATTTACCTTACTTTTTAAAAACTACAAAGTAGCATAATTTGTTCTACATTTATTTGAAAAGTAAGTAAT
  TTTAATCTCTTTTTTAGTGGGAATATGTGGGCATGAAAATTAGATACCCAACTTAAACCAAAGGCATGTC
  TATCATGTGGATGCAGTAACATTTACATTTAGTTTTTGATCGTAGTTTTATATGAATGTTCCAAGAAAAA
  AGCAGACTGTTACAAATAAGTTAAAACTGATATGATTGATAGGTTCTGTTTTTTCTTGAAGCCTATGTAT
  TTGGTAAGAAGAAATACTACCGAAGTAAAATATAATGTACCTAGATTGTAGGAGATGACAGACATAAGGT
  ATTTCAAAATAAATCTCAGGTGCTATAACATGTAGTCATCTGTTTTCTGATAAGAACATCTTTTACTCTG
  ACTTGCTTTTATCTTAGTAGTATGCTTATGGATTTAGTAGTATGCTTATGGATTTGATAAATCTTATACT
  TTTTCAGTTGCTGTCTTATTCTCTTTATTTCTCATTGTGCTTTCCCTTCCCTTCT
  
  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_001142766.1
• Summary: This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]
• Locus ID: 65217