WDR65 (CFAP57) (NM_001167965) Human Untagged Clone

CAT#: SC329079

WDR65 (untagged)-Human WD repeat domain 65 (WDR65) transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: CFAP57
• Synonyms: VWS2; WDR65
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001167965, the custom clone sequence may differ by one or more nucleotides
  ATGTCAGCCGTGGTAGCTCAGACGCTGCATGTTTTTGGTCTTCGATCCCACGTGGCCAAC
  AATATCTTCTACTTCGATGAACAGATCATTATATTTCCTTCAGGAAATCACTGTGTGAAG
  TACAATGTGGATCAGAAATGGCAAAAATTCATTCCAGGCTCAGAGAAGAGTCAGGGCATG
  TTGGCCTTGTCCATCAGTCCCAATCGGCGGTACCTCGCTATCTCTGAGACTGTGCAAGAA
  AAACCTGCCATCACCATTTATGAATTGTCATCCATCCCTTGCCGGAAGCGCAAAGTTCTT
  AATAATTTTGACTTCCAAGTTCAGAAATTTATTAGCATGGCTTTTTCTCCAGACTCCAAA
  TACCTATTGGCTCAGACGTCACCTCCAGAGTCAAATCTTGTCTACTGGCTGTGGGAAAAA
  CAGAAAGTAATGGCCATTGTTAGAATCGACACTCAGAACAACCCTGTCTACCAGGTGAGC
  TTCAGTCCACAGGATAACACTCAGGTGTGTGTCACTGGAAATGGGATGTTTAAGCTTCTC
  CGTTTTGCTGAGGGAACCCTGAAGCAAACCAGCTTTCAGAGGGGAGAACCCCAAAACTAT
  CTAGCTCACACCTGGGTGGCTGATGACAAGATTGTCGTTGGCACTGACACAGGCAAACTC
  TTCCTCTTTGAATCTGGAGATCAGCGTTGGGAGACCAGCATAATGGTCAAGGAACCTACC
  AATGGCTCAAAGAGCCTGGATGTCATTCAGGAATCAGAGAGCCTGATTGAATTTCCACCA
  GTCAGTTCTCCACTCCCTTCCTATGAACAGATGGTGGCGGCCAGTAGCCATAGCCAGATG
  TCCATGCCCCAGGTGTTTGCCATTGCAGCCTATTCAAAGGGATTTGCCTGTTCTGCTGGG
  CCAGGGAGAGTTCTGCTGTTTGAGAAGATGGAAGAAAAGGATTTTTACCGTGAGAGCAGA
  GAAATCAGGATTCCTGTGGACCCGCAGAGCAATGATCCAAGTCAGTCTGACAAACAGGAC
  GTTCTCTGCCTGTGCTTCAGCCCCTCAGAGGAAACTCTGGTTGCCAGCACCAGTAAGAAC
  CAACTCTACAGCATCACCATGTCCCTGACAGAGATCAGCAAGGGGGAGCCTGCTCACTTT
  GAGTATTTGATGTATCCATTGCACTCAGCACCCATCACCGGTCTAGCTACCTGCATCCGC
  AAACCCCTTATAGCCACCTGTTCTCTGGATCGATCCATCCGCCTTTGGAATTATGAAACA
  AACACCCTGGAACTATTTAAGGAATACCAAGAAGAGGCATATTCCATCAGCCTTCATCCA
  TCTGGACACTTCATTGTAGTAGGGTTTGCTGACAAACTACGCCTCATGAATCTACTCATT
  GATGATATACGTTCTTTCAAAGAATACTCTGTTAGAGGATGCGGAGAGTGTTCCTTTAGC
  AATGGAGGTCACCTGTTTGCTGCAGTCAATGGAAATGTGATTCACGTTTACACCACCACG
  AGCCTAGAGAACATCTCAAGCCTGAAAGGACACACAGGGAAGATTCGCTCAATTGTGTGG
  AATGCAGATGATAGCAAACTGATTTCTGGTGGCACAGATGGTGCTGTGTATGAATGGAAT
  CTGTCCACAGGAAAGAGAGAGACAGAATGCGTGCTCAAGTCTTGCAGCTACAACTGTGTT
  ACTGTCTCCCCCGATGCCAAAATTATCTTTGCTGTTGGATCAGACCACACCCTCAAGGAG
  ATTGCAGATTCCTTGATCCTTCGAGAGATATCGGCGTTTGATGTCACCTACACCGCCATT
  GTCATCTCGCATTCTGGACGCATGATGTTTGTGGGCACCTCGGTGGGAACCATTCGTGCC
  ATGAAGTACCCTCTGCCTCTGCAGAAGGAATTCAATGAGTACCAGGCCCATGCCGGTCCT
  ATCACCAAGGTGAGCAGGGCCCTCTCCCCAGGAACCCAGTCCCACACCTGCCTGCTACGT
  GCCTTGTTCATCCCTTCAACCTCCCAATGTCTTTTCTCTCTCCTTCTTCTCTCTTATTTA
  TTCATCCATCATTCATTGAATCACCATCTATTGACTATGAATATACTCTTTGTTTAA
  
• Restriction Sites: Please inquire
• ACCN: NM_001167965
• 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_001167965.1, NP_001161437.1
• RefSeq Size: 3034
• 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 (3) differs in both UTRs 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.