Adenosine A2b Receptor (ADORA2B) (NM_000676) Human 3' UTR Clone

CAT#: SC207431

3`UTR clone of adenosine A2b receptor (ADORA2B) 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: ADORA2B
• Synonyms: ADORA2
• ACCN: NM_000676
• Insert Size: 569
• Sequence Data:
  Insert Sequence

  >SC207431 3'UTR clone of NM_000676
  The sequence shown below is from the reference sequence of NM_000676. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon
  
  
  CAATTGGCAGAGCTCAGAATTCAAGCGATCGC
  
  TACAGCCTGCTCTCGGTGTGGGCCTATGATCTAGGCTCTCGCCTCTTCCAGGAGAAGATACAAATCCACA
  AGAAACAAAGAGGACACGGCTGGTTTTCATTGTGAAAGATAGCTACACCTCACAAGGAAATGGACTGCCT
  CTCTTGAGCACTTCCCTGGAGCTACCACGTATCTAGCTAATATGTATGTGTCAGTAGTAGGCTCCAAGGA
  TTGACAAATATATTTATGATCTATTCAGCTGCTTTTACTGTGTGGATTATGCCAACAGCTTGAATGGATT
  CTAACAGACTCTTTTGTTTTTAAAAGTCTGCCTTGTTTATGGTGGAAAATTACTGAAACTATTTTACTGT
  GAAACAGTGTGAACTATTATAATGCAAATACTTTTTAACTTAGAGGCAATGGAAAAATAAAAGTTGACTG
  TACTAAAAATGTATACTTGTTGCCAGGAAGGTGACCTCAAAAATTAAAAGTATAATTATTCGGCCGGGCA
  TGGTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGTTCA
  AAACCAGCC
  
  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_000676.2
• Summary: This gene encodes an adenosine receptor that is a member of the G protein-coupled receptor superfamily. This integral membrane protein stimulates adenylate cyclase activity in the presence of adenosine. This protein also interacts with netrin-1, which is involved in axon elongation. The gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
• Locus ID: 136