SLC33A1 (NM_004733) Human 3' UTR Clone

CAT#: SC208277

3`UTR clone of solute carrier family 33 (acetyl-CoA transporter) member 1 (SLC33A1) 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: SLC33A1
• Synonyms: ACATN; AT-1; AT1; CCHLND; SPG42
• ACCN: NM_004733
• Insert Size: 656
• Sequence Data:
  Insert Sequence

  >SC208277 3'UTR clone of NM_004733
  The sequence shown below is from the reference sequence of NM_004733. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  GAAGGATCATCTTCGTGGAAATGCAAAAGGAACAATTAATATATATGCTACTGGACATTCTAGCAAGGTA
  ATTGTAGTTTAGTTTTAATTCGGAGAGCAATGATAATCAGTGCACAGGAGTATAAAATATTATTTTAAAC
  AGCGAAATTAATAATATAAAATGCCAAATGGTTGAAAAAATAGAAACCTTTCTGTATATTTGATCATATT
  TTTTTTTTGCCTTGTCAATGTATTTAAAGTTTACTTAAGGTCAGGAAATTCTAAAACAACTTTTCTGGCC
  TTGTTATTTGATGTATATCTTTTAAATTTACTGACCAAAGCATGTTTTAAGCTGCAATGCAGTAGTCACG
  GGTGGTAACCATGTAGTCAGGTATTGTTATTAGTACCTATCACTGCTGAGCTGTATTTAAAATTTTGGTA
  CAATATATAAAATGGAGAAGAGCTTGATATTCAGGTACTAACCACAACTAGTCTGACATTGTTGGCAGTT
  AAAATCTTATTTTGAATTGTAAATTAGTTAAATTTTATGTGGAATTTGCTGAGAAAAGAATATAGACTAC
  TGAAATGTCATTTTAGTTATTTTTCTTATGACCACATTGTACAAATGAATCTGTGTTAAAAAGACTATTT
  TAAATGTATTTCCTGCTTTTGTAAGC
  
  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_004733.2
• Summary: The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]
• Locus ID: 9197