RDH12 (NM_152443) Human 3' UTR Clone

CAT#: SC208582

3`UTR clone of retinol dehydrogenase 12 (all-trans/9-cis/11-cis) (RDH12) 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: RDH12
• Synonyms: LCA13; RP53; SDR7C2
• ACCN: NM_152443
• Insert Size: 621
• Sequence Data:
  Insert Sequence

  >SC208582 3'UTR clone of NM_152443
  The sequence shown below is from the reference sequence of NM_152443. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  GCCTATGGAATGTCAGCTGTGAGCTTCTAGGAATCCGGTGGGAGTAGCTGGTGGAAGAGCTGCAGCTTTA
  TCAGGCCCAATCCATGCCATAATGAACAGGGACCAAGGAGAAGGCCAACCCTAAAGGATTGTCCTCTTGG
  CCAGCTGGTGCTGCGAATCCTGCCTGCTCTGATCCTCTTGACCCTTCTGGGAATGTTTGCACACCTGACA
  CTCTTGTGAGACTGGCTTATGGCATGAGTTGTGGACACCTATAGAGTGTTCTTCTCTAAGACCTGGAAAG
  TCAGCAACCCTCTGGGGGCAGCAGGACTGGGCAGATCCCAGGCTGGGCATGGGGGTGGCAGAAGAGCCCG
  AGAAATTGGGTCAGTTCCCTCATCAGCACCAGAGGCTCAGCTGAGGCAAGAAGAGCACCATCACTGCCTA
  TTTCTAGGGGCTATACACTCCAACTCTTGGTTGATCTCTTTCTTTTTAAAAATATTTGCCACCACCCTGG
  AGTCTAGACCAACACACAAAGATCCTGGCTAACCCTGGCCTATTTAGATTCCTTCCTCTCACCTGGACCT
  TCCCATTTCAATCATGCAGATGGTTTCTTTTTGTAAAGAGTTCCGTTTGCCTTTCAATTTT
  
  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_152443.2
• Summary: The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]
• Locus ID: 145226