Cdc14a (NM_001134856) Rat Untagged Clone

CAT#: RN200086

Cdc14a (untagged ORF) - Rat CDC14 cell division cycle 14 homolog A (S. cerevisiae) (Cdc14a), transcript variant 1, (10 ug)

Specifications

Product Data

• Type: Rat Untagged Clone
• Tag: Tag Free
• Symbol: Cdc14a
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >RN200086 representing NM_001134856
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGGCAGCGGAGTCAGGGGAACTAATCGGGGCTTGCGAGTTCATGAAAGATCGATTATATTTTGCTACTT
  TAAGGAATAGACCAAAAAGCACAATAAATATCCACTATTTCTCCATCGACGAGGAGCTGGTCTATGAAAA
  TTTCTATGCAGATTTTGGACCTCTGAACTTGGCAATGGTGTACAGATACTGCTGTAAGCTAAACAAGAAA
  CTAAAATCATACAGTTTATCAAGAAAGAAAATAGTGCACTACACCTCTTTCGACCAGCGGAAAAGAGCAA
  ACGCAGCATTCTTGATAGGTGCTTATGCCGTCATCTACTTAAAGAAGACACCAGAAGAAGCGTACAGAGC
  TCTCCTGTCTGGCTCAAACCCTCCTTATCTTCCATTCAGGGATGCGTCCTTTGGAAATTGCACTTACAAC
  CTCACCGTCCTTGACTGTTTACAAGGAATCAGAAAGGGATTACAGCATGGATTTTTTGACTTTGAGACAT
  TTGATGCGGATGAATATGAACACTATGAGCGAGTTGAAAATGGGGACTTCAACTGGATCGTTCCAGGAAA
  ATTTTTAGCATTTAGTGGACCACATCCTAAAAGCAAAATTGAAAATGGTTACCCTCTCCACGCTCCTGAA
  GCCTACTTTCCGTATTTCAAAAAGAACAACGTGACAACAATCGTGAGATTGAATAAAAAGATTTATGAGG
  CGAAGCGCTTCACAGACGCTGGCTTCGAGCACTACGACCTGTTCTTCATAGATGGCAGCACCCCCAGCGA
  CAACATCGTGCGAAGATTCCTGAACATCTGTGAGAACACGGAGGGGGCCATTGCGGTCCACTGCAAAGCT
  GGTCTGGGGAGAACTGGGACTTTGATAGCCTGTTACGTCATGAAACACTACAGGTTCACACACGCTGAAA
  TCATCGCTTGGATCAGAATTTGTCGACCAGGCTCCATCATTGGACCCCAGCAGCATTTCCTGGAAGAGAA
  ACAAGCATCATTGTGGGTCCAAGGAGACATTTTTCGATCCAAACTGAAAAATAGACCGTCCAGTGAAGGA
  AGTATTACTAAAATTATTTCTAGCTTGGATGATATGTCTATTGCTGGGAACTTATCTAAATTACAAAGCA
  CAGAAAGGATTGGAGAGAATAATTTTGAAGACGAAGATATGGAAATTAAAAACAACGTAACGCAGGGAGA
  CAAACTACGTGCCTTAAAAAGCCAGAGGCAGCCCCGCTCCTCGCCATCCTGTGCATTTAGGTCAGATGAT
  ATGAAAGGACACCAAAGGGCAGTGGCCCAGACTTTCAGATTAAGTTCTTCACCACAACCAACAGTGCCGA
  CTGTGAAGACCCCCAAAGTGTGTTTGTCCCCTTCAGTGACAGCCAAAAGGATAAGCAGAGGTTCTCTGTC
  TTCAGGAGCAAACATAAGAAGCTTCTCCATAAATTCCCGGCTAGCCAGTTCCCTGGGGAACTTGAATTCT
  GGGACAGAAGAAACTGAGAACAAAAAGACCACATCACCCATCAAGGCTGCTTTCATAGCCAGCCCGTTCA
  CCAGCTTCTTGAATGGCAGCACCCAGACACCTGGCAGAAACTACCCTGAGCTCAACAACAATCAGTACAC
  CAGAAGCAGCAACAGCAGCAGCGGCGGCAGTCTTGGGGGCAACCTGAACAGCTCTCCAAGCGCCAAGCCC
  GAGGAGCATAACACCATCCTTAGACCTTCCTTCTCGGGGGCGCTCTCTTCCTCCTCAGTGAGATTCCTGA
  GCCGTTCTATACCTTCCCTTCAGTCTGAATATGTTCATTACTAA
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_001134856
• ORF Size: 1794 bp
• Insert Size: 1794
• 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).

Reference Data

• RefSeq: NM_001134856.1, NP_001128328.1
• RefSeq Size: 4476
• RefSeq ORF: 1794
• Locus ID: 310806
• Gene Summary: The protein encoded by this gene is a dual-specificity phosphatase that preferentially dephosphorylates cyclin dependent kinase substrates to regulate the cell cycle. In human cell lines, this protein localizes to interphase chromosomes, and depletion of the transcript results in centrosome separation and cytokinesis defects. In mouse, the protein localizes to the nucleus of prophase I arrested oocytes and then becomes dispersed in meiotically competent oocytes. Knockdown of the protein delays exit from metaphase I and results in eggs with chromosomal abnormalities and elevated aneuploidy, demonstrating a function in regulation of meiosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]
  Transcript Variant: This variant (1) represents the longer transcript. It encodes isoform 1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments.