RAI2 (NM_001172732) Human Untagged Clone

CAT#: SC328786

RAI2 (untagged)-Human retinoic acid induced 2 (RAI2) transcript variant 4

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: RAI2
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001172732, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGACGACCTGCAGTCCCAGAACCTCTCCATGGACATGACTGACTCCCCTCCTGCCTTGGCTAATAACA
  GACTGGAGAATGGCATGGCTCAGCTGATCACCACCGAGGCCTGGAACATCAACTCCACTGACCTGGTGGA
  GGGAAGCTCCGCACCAGAGCTCAATCCGAATGGCAATGCCACCTACGTCATGACCACCCAGGGCCCCGTG
  CAACTGCCCGTGGTGCTGGAGCAGCACGTCTTTCAGCACCTCAACTCCCCTCTGGTCCTGCCGCAGGAGG
  CCCCATGCTCCTCCAGTACCATCCACAACAACCTCTTCCAGGGAGCGGAGGACCCCGAGGCCCAGCCCCA
  GCTCCTGGACCTGAGGATCCCCAGCCAGCCGCAGGAGCCCACTTTGCCATTTGAAGCTGTGCTCCAGAAT
  TTGTTTCCCTCCCAGGGCACTCTCGGGCCCCCACCCTGTCAGCCTCCTCCTGGCTATGCCCCTGTGCCCC
  CACAGCCTTTTAGCTCCCCCTTGTCCCCCCTGGTCCCACCAGCCACCCTCTTGGTGCCGTATCCTGTAAT
  CGTCCCCTTGCCTGTGCCAGTCCCTATTCCCATCCCCATCCCGGTGCCTCAGAGTTCTGAATCCAAGTTC
  AGCTCCAGTTTCCCCAAGCCACCATCTTCCTTCGGCCTGCACCCCTTTAAAGGCACCCAGACCCCTCTGG
  AAAAAGATGAACTGAAGCCCTTTGACATCCTCCAGCCTAAGGAGTACTTCCAGCTCAGCCGCCACACGGT
  CATTAAGATGGGAAGTGAGAACGAGGCCCTGGATCTCTCCATGAAGTCAGTGCCCTGGCTCAAGGCTGGT
  GAAGTCAGTCCCCCAATCTTCCAGGAAGATGCAGCCCTAGACCTGTCAGTGGCAGCCCACCGGAAATCCG
  AGCCTCCCCCTGAGACACTGTATGACAGTGGTGCATCAGTGGACAGCTCAGGTCACACAGTGATGGAGAA
  ACTTCCCAGTGGCATGGAAATTTCTTTTGCCCCTGCCACGTCCCATGAGGCCCCAGCCATGATGGATAGT
  CACATCAGCAGCAGTGATGCTGCTACCGAGATGCTCAGCCAGCCCAACCACCCCAGCGGCGAAGTCAAGG
  CTGAAAATAACATTGAGATGGTGGGCGAGTCCCAGGCGGCCAAGGTCATTGTCTCTGTCGAAGATGCTGT
  GCCTACCATATTCTGTGGCAAGATCAAAGGCCTCTCAGGGGTGTCCACCAAAAACTTCTCCTTCAAAAGA
  GAAGACTCCGTGCTTCAGGGCTATGACATCAACAGCCAAGGGGAAGAGTCCATGGGAAATGCAGAGCCCC
  TTAGGAAACCCATCAAAAACCGGAGCATAAAGTTAAAGAAAGTGAACTCCCAGGAAATACACATGCTCCC
  AATCAAAAAACAACGGCTGGCCACCTTTTTTCCAAGAAAGTAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001172732
• ORF Size: 1443 bp
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
• OTI Annotation: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.

Reference Data

• RefSeq: NM_001172732.1, NP_001166203.1
• RefSeq Size: 2079
• RefSeq ORF: 1443
• Locus ID: 10742
• Gene Summary: Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
  Transcript Variant: This variant (4) differs in the 5' UTR and lacks a segment in the coding region, compared to variant 1. The resulting protein (isoform 2) is shorter than isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.