CFAP298 (NM_021254) Human Untagged Clone

CAT#: SC319422

C21orf59 (untagged)-Human chromosome 21 open reading frame 59 (C21orf59), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: CFAP298
• Synonyms: C21orf48; C21orf59; CILD26; FBB18; Kur
• Vector: pCMV6-AC
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_021254.1 CTGTGAGCGGCTGTTAGTGCGTCGCAGCTGCTGGCGATCCGGCGACCCTCGGCCGGCAGG
  ACCCGCGGGCCACGCAGCCGGGGCCTTCTCAACGCCTCAGTACCTCGGCGGGACCGCCAT
  GGTTCTGCTGCACGTGAAGCGGGGCGACGAGAGCCAGTTCCTGCTGCAGGCGCCTGGGAG
  TACCGAGCTGGAGGAGCTCACGGTGCAGGTGGCCCGGGTCTATAATGGGCGGCTCAAGGT
  GCAGCGCCTCTGCTCAGAAATGGAAGAATTAGCCGAACATGGCATATTTCTCCCTCCTAA
  TATGCAAGGACTGACCGATGATCAGATTGAAGAATTGAAATTGAAGGATGAATGGGGTGA
  AAAATGCGTACCCAGCGGAGGTGCAGTGTTTAAAAAGGATGATATTGGACGAAGGAATGG
  GCAAGCTCCAAATGAGAAGATGAAGCAAGTGTTAAAGAAGACTATAGAAGAAGCCAAAGC
  AATAATATCTAAGAAACAAGTGGAAGCCGGTGTCTGTGTTACCATGGAGATGGTGAAAGA
  TGCCTTGGACCAGCTTCGAGGCGCGGTGATGATTGTTTACCCCATGGGGTTGCCACCGTA
  TGATCCCATCCGCATGGAGTTTGAAAATAAGGAAGACTTGTCGGGAACACAGGCAGGGCT
  CAACGTCATTAAAGAGGCAGAGGCGCAGCTGTGGTGGGCAGCCAAGGAGCTGAGAAGAAC
  GAAGAAGCTTTCAGACTACGTGGGGAAGAATGAAAAAACCAAAATTATCGCCAAGATTCA
  GCAAAGGGGACAGGGAGCTCCAGCCCGAGAGCCTATTATTAGCAGTGAGGAGCAGAAGCA
  GCTGATGCTGTACTATCACAGAAGACAAGAGGAGCTCAAGAGATTGGAAGAAAATGATGA
  TGATGCCTATTTAAACTCACCATGGGCGGATAACACTGCTTTGAAAAGACATTTTCATGG
  AGTGAAAGACATAAAGTGGAGACCAAGATGAAGTTCACCAGCTGATGACACTTCCAAAGA
  GATTAGCTCACCTTTCTCCTAGGCAATTATAATTTAAAAAAAAAAAAAAAAAA
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_021254.1 unedited
  GCAGCGGTCGGGGGTATATGGTCATTGTATACGACTCCTATAGGGCGGCCGGGAATTCGG
  CACGAGGCTGTGAGCGGCTGTTAGTGCGTCGCAGCTGCTGGCGATCCGGCGACCCTCGGC
  CGGCAGGACCCGCGGGCCACGCAGCCGGGGCCTTCTCAACGCCTCAGTACCTCGGCGGGA
  CCGCCATGGTTCTGCTGCACGTGAAGCGGGGCGACGAGAGCCAGTTCCTGCTGCAGGCGC
  CTGGGAGTACCGAGCTGGAGGAGCTCACGGTGCAGGTGGCCCGGGTCTATAATGGGCGGC
  TCAAGGTGCAGCGCCTCTGCTCAGAAATGGAAGAATTAGCCGAACATGGCATATTTCTCC
  CTCCTAATATGCAAGGACTGACCGATGATCAGATTGAAGAATTGAAATTGAAGGATGAAT
  GGGGTGAAAAATGCGTACCCAGCGGAGGTGCAGTGTTTAAAAAGGATGATATTGGACGAA
  GGAATGGGCAAGCTCCAAATGAGAAGATGAAGCAAGTGTTAAAGAAGACTATAGAAGAAG
  CCAAAGCAATAATATCTAAGAAACAAGTGGAAGCCGGTGTCTGTGTTACCATGGAGATGG
  TGAAAGATGCCTTGGACCAGCTTCGAGGCGCGGTGATGATTGTTTACCCCATGGGGTTGC
  CACCGTATGATCCCATCCGCATGGAGTTTGAAAATAAAGGAAGACTTGTCGGGAACACAG
  GCAGGGCTCAACGTCATTAAAGAGGCAGAGGCGCAGCTGTGGTGGGGCAGCCAAGGAGCT
  GAGAGACGAAGAAGCTTTCAGACTACGTGGGGGAGATGAAAAAACCAAAATTATCGCCAG
  ATTCAGCAAGGGACAGGGAGCTCCAGGCCGGAGAAGCTATTATTAGCATGAGGAGCAGAA
  GCAGCTGATGCTGTACTATCCAGAGAACAAGAGGGAGCTCAGAGAATGCAGGAATGATGA
  TGAGTGCCTATTTAACTTCACCCATGGGGCGG
• Restriction Sites: Please inquire
• ACCN: NM_021254
• ORF Size: 873 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_021254.1, NP_067077.1
• RefSeq Size: 1064
• RefSeq ORF: 873
• Locus ID: 56683
• Gene Summary: This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]
  Transcript Variant: This variant (1) represents the longest transcript and encodes the longest 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.