Synphilin 1 (SNCAIP) (NM_005460) Human 3' UTR Clone

CAT#: SC207980

3`UTR clone of synuclein alpha interacting protein (SNCAIP) 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: SNCAIP
• Synonyms: Sph1; SYPH1
• ACCN: NM_005460
• Insert Size: 609
• Sequence Data:
  Insert Sequence

  >SC207980 3'UTR clone of NM_005460
  The sequence shown below is from the reference sequence of NM_005460. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  AGCTCCGCTAGCAAAGGAAAGAATAAGGCAGCATAATGACATCAATAGAAAAATGAAGAAATCCTACAGC
  ATAAAGCACATTGCTGAGCCAGAGTCAAAAGAACTCTTCTTGTAAATCACTTTTTAAATTTTCTCTCACT
  GATGCCCTTTGGAAATTATTGGAAATTTCTGGACTATCCTCTTTGGAAAGAGAACCATGAAAACAATGCC
  TCACCAGCAGAAGAACAGAATATCAGGATGCCTTAAATTTATAGTAGTAGACTGTAAAAGATTCATTTTG
  GGGTGATATCTGTATATATAACTTGTTTTTTTAAAAGATGCCGTTTAAAAGCATGATTGGGAAAATGTAT
  GTTTTTTAAGAGTAGATTGATTCACCCTACCCACAGGACATTCACCAAGCCACTGATACCATTTTATATT
  TCATCAATTGCATGAGTATTTGCTAATGTTGATTGAACCTCCCTTTCCCCATAATGTGGGCAGATTTGGC
  TCAGCTCCTTCATGAGATCAGGTCAGTGGTATTGTTTCTGTCAAGAGTGTTTTTTCTGTCATTTCTACTT
  TTTGTATAAAGGAAATAAAACAATGTTAACAGCCACCTATAAGCTTGGG
  
  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_005460.2
• Summary: This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
• Locus ID: 9627