WDR65 (CFAP57) (NM_152498) Human Untagged Clone

CAT#: SC306421

WDR65 (untagged)-Human WD repeat domain 65 (WDR65), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: CFAP57
• Synonyms: VWS2; WDR65
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_152498, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGTCAGCCGTGGTAGCTCAGACGCTGCATGTTTTTGGTCTTCGATCCCACGTGGCCAACAATATCTTCT
  ACTTCGATGAACAGATCATTATATTTCCTTCAGGAAATCACTGTGTGAAGTACAATGTGGATCAGAAATG
  GCAAAAATTCATTCCAGGCTCAGAGAAGAGTCAGGGCATGTTGGCCTTGTCCATCAGTCCCAATCGGCGG
  TACCTCGCTATCTCTGAGACTGTGCAAGAAAAACCTGCCATCACCATTTATGAATTGTCATCCATCCCTT
  GCCGGAAGCGCAAAGTTCTTAATAATTTTGACTTCCAAGTTCAGAAATTTATTAGCATGGCTTTTTCTCC
  AGACTCCAAATACCTATTGGCTCAGACGTCACCTCCAGAGTCAAATCTTGTCTACTGGCTGTGGGAAAAA
  CAGAAAGTAATGGCCATTGTTAGAATCGACACTCAGAACAACCCTGTCTACCAGGTGAGCTTCAGTCCAC
  AGGATAACACTCAGGTGTGTGTCACTGGAAATGGGATGTTTAAGCTTCTCCGTTTTGCTGAGGGAACCCT
  GAAGCAAACCAGCTTTCAGAGGGGAGAACCCCAAAACTATCTAGCTCACACCTGGGTGGCTGATGACAAG
  ATTGTCGTTGGCACTGACACAGGCAAACTCTTCCTCTTTGAATCTGGAGATCAGCGTTGGGAGACCAGCA
  TAATGGTCAAGGAACCTACCAATGGCTCAAAGAGCCTGGATGTCATTCAGGAATCAGAGAGCCTGATTGA
  ATTTCCACCAGTCAGTTCTCCACTCCCTTCCTATGAACAGATGGTGGCGGCCAGTAGCCATAGCCAGATG
  TCCATGCCCCAGGTGTTTGCCATTGCAGCCTATTCAAAGGGATTTGCCTGTTCTGCTGGGCCAGGGAGAG
  TTCTGCTGTTTGAGAAGATGGAAGAAAAGGATTTTTACCGTGAGAGCAGAGAAATCAGGATTCCTGTGGA
  CCCGCAGAGCAATGATCCAAGTCAGTCTGACAAACAGGACGTTCTCTGCCTGTGCTTCAGCCCCTCAGAG
  GAAACTCTGGTTGCCAGCACCAGTAAGAACCAACTCTACAGCATCACCATGTCCCTGACAGAGATCAGCA
  AGGGGGAGCCTGCTCACTTTGAGTATTTGATGTATCCATTGCACTCAGCACCCATCACCGGTCTAGCTAC
  CTGCATCCGCAAACCCCTTATAGCCACCTGTTCTCTGGATCGATCCATCCGCCTTTGGAATTATGAAACA
  AACACCCTGGAACTATTTAAGGAATACCAAGAAGAGGCATATTCCATCAGCCTTCATCCATCTGGACACT
  TCATTGTAGTAGGGTTTGCTGACAAACTACGCCTCATGAATCTACTCATTGATGATATACGTTCTTTCAA
  AGAATACTCTGTTAGAGGATGCGGAGAGTGTTCCTTTAGCAATGGAGGTCACCTGTTTGCTGCAGTCAAT
  GGAAATGTGATTCACGTTTACACCACCACGAGCCTAGAGAACATCTCAAGCCTGAAAGGACACACAGGGA
  AGATTCGCTCAATTGTGTGGAATGCAGATGATAGCAAACTGATTTCTGGTGGCACAGATGGTGCTGTGTA
  TGAATGGAATCTGTCCACAGGAAAGAGAGAGACAGAATGCGTGCTCAAGTCTTGCAGCTACAACTGTGTT
  ACTGTCTCCCCCGATGCCAAAATTATCTTTGCTGTTGGATCAGACCACACCCTCAAGGAGATTGCAGATT
  CCTTGATCCTTCGAGAGATATCGGCGTTTGATGTCACCTACACCGCCATTGTCATCTCGCATTCTGGACG
  CATGATGTTTGTGGGCACCTCGGTGGGAACCATTCGTGCCATGAAGTACCCTCTGCCTCTGCAGAAGGAA
  TTCAATGAGTACCAGGCCCATGCCGGTCCTATCACCAAGGTGAGCAGGGCCCTCTCCCCAGGAACCCAGT
  CCCACACCTGCCTGCTACGTGCCTTGTTCATCCCTTCAACCTCCCAATGTCTTTTCTCTCTCCTTCTTCT
  CTCTTATTTATTCATCCATCATTCATTGAATCACCATCTATTGACTATGAATATACTCTTTGTTTAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_152498
• ORF Size: 2097 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_152498.3, NP_689711.2
• RefSeq Size: 3037
• RefSeq ORF: 2097
• Locus ID: 149465
• Gene Summary: This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member is thought to function in craniofacial development, possibly in the fusion of lip and palate. A missense mutation in this gene is associated with Van der Woude syndrome 2. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]
  Transcript Variant: This variant (1) differs in the 3' UTR and lacks several exons in the 3' coding region, but includes an alternate 3' exon, compared to variant 5. The resulting isoform (b, also known as WDR65b) has a shorter and distinct C-terminus, compared to isoform a. Both variants 1 and 3 encode isoform b. 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.