NSUN5 (NM_001168348) Human Untagged Clone

CAT#: SC328620

NSUN5 (untagged)-Human NOP2/Sun domain family member 5 (NSUN5) transcript variant 4

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: NSUN5
• Synonyms: NOL1; NOL1R; NSUN5A; p120; p120(NOL1); WBSCR20; WBSCR20A
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001168348, the custom clone sequence may differ by one or more nucleotides
  ATGGGGCTGTATGCTGCAGCTGCAGGCGTGTTGGCCGGCGTGGAGAGCCGCCAGGGCTCT
  ATCAAGGGGTTGGTGTACTCCAGCAACTTCCAGAACGTGAAGCAGCTGTACGCGCTGGTG
  TGCGAAACGCAGCGCTACTCCGCCGTGCTGGATGCTGTGATCGCCAGCGCCGGCCTCCTC
  CGTGCGGAGAAGAAGCTGCGGCCGCACCTGGCCAAGGTTCATCGGGGTGTGAGCCGGAAT
  GAGGACCTGTTGGAAGTGGGATCCAGGCCTGGTCCAGCCTCCCAGCTGCCTCGATTTGTG
  CGTGTGAACACTCTCAAGACCTGCTCCGATGATGTAGTTGATTATTTCAAGAGACAAGGT
  TTCTCCTATCAGGGTCGGGCTTCCAGCCTCGATGACTTACGAGCCCTCAAGGGGAAGCAT
  TTTCTCCTGGACCCCTTGATGCCGGAGCTGCTGGTGTTTCCCGCCCAGACAGATCTGCAT
  GAACACCCACTGTACCGGGCCGGACACCTCATTCTGCAGGACAGGGCCAGCTGTCTCCCA
  GCCATGCTGCTGGACCCCCCGCCAGGCTCCCATGTCATCGATGCCTGTGCCGCCCCAGGC
  AATAAGACCAGTCACTTGGCTGCTCTTCTGAAGAACCAAGGGAAGATCTTTGCCTTTGAC
  CTGGATGCCAAGCGGCTGGCATCCATGGCCACGCTGCTGGCCCGGGCTGGCGTCTCTTGC
  TGTGAACTGGCTGAGGAGGACTTCCTGGCGGTCTCCCCCTCGGATCCACGCTACCATGAG
  GTCCACTACATCCTGCTGGATCCTTCCTGCAGTGGCTCGGGTATGCCGAGCAGACAGCTG
  GAGGAGCCCGGGGCAGGCACACCTAGCCCGGTGCGTCTGCATGCCCTGGCAGGGTTCCAG
  CAGCGAGCCCTGTGCCACGCGCTCACTTTCCCTTCCCTGCAGCGGCTCGTCTACTCCACG
  TGCTCCCTCTGCCAGGAGGAGAATGAAGACGTGGTGCGAGATGCGCTGCAGCAGAACCCG
  GGCGCCTTCAGGCTAGCTCCCGCCCTGCCTGCCTGGCCCCACCGAGGCCTGAGCACGTTC
  CCGGGTGCCGAGCACTGCCTCCGGGCCTCCCCTGAGACCACACTCAGCAGTGGCTTCTTC
  GTTGCTGTAATTGAACGGGTCGAGGTGCCAAGGTGA
  
• Restriction Sites: Please inquire
• ACCN: NM_001168348
• ORF Size: 1176 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_001168348.1, NP_001161820.1
• RefSeq Size: 2332
• RefSeq ORF: 1176
• Locus ID: 55695
• Gene Summary: This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
  Transcript Variant: This variant (4) uses an alternate in-frame splice site in the 5' coding region and includes an alternate segment in the 3' coding region, which results in a frameshift, compared to variant 1. The encoded isoform (4) is shorter and has a distinct C-terminus, compared to isoform 1.