Ocrl (NM_001108256) Rat Untagged Clone

CAT#: RN204922

Ocrl (untagged ORF) - Rat oculocerebrorenal syndrome of Lowe (Ocrl), (10 ug)

Specifications

Product Data

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

  >RN204922 representing NM_001108256
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGGAGCCGCGGCTCCCGATCGGAGCTCAGCCCCTGGCAATGGTGGCGGGTTTGGAGATGAAGGGTCCTC
  TCCGGGAGCCCTGCGTCCTGACCCTAGCCCGGAGGAACGGGCAATATGAGTTAATAATCCAGTTGCATGG
  GAAGGAACAGCATGTTCAAGATATCATTCCTATAAATAGCCACTTCAGATGTGTTCAAGAAGCAGAAGAA
  ACTCTTTTGATTGATATTGCTTCAAACAGTGGCTGCAAAATTCGGGTACAGGGAGACTGGACCAGAGAGC
  GCCACTTTGAAATTCCTGATGAAGAACGCTGTTTGAAGTTCCTCTCAGAGGTCCTTGCTGCTCAGGAAGC
  TCAGTCACAGCTTCTTGTTCCAGAACAAAAAGACTCATCTAACTGGTACCAGAAATTAGACACTAAGGAT
  AAACCTGCTTATTCAGGACTGCTTGGATTTGAAGATAATTTTTCATCTATGAATTTAGATAAAAAAATGA
  ATACACAAAATCCCCCCACAGGGATTCATCGGGAACCACCCCCTCCACCTTCTTCAAATAGAATGCTTCC
  ACGTGAAAAGGAAGCTTTAAACAAAGAACAGCCCAAAGTGACCAATACCATGCGGAAGCTGTTCGCACCA
  AACAGCCAATCTGGCCAGCGAGAGGGTCTCATCAAACACATCCTTGCAAAGCGAGAGAAAGAGTATGTCA
  ACATCCAGTCTTTCAGATTTTTTGTTGGAACTTGGAATGTGAATGGCCAGTCTCCAGACAGCAGCTTAGA
  ACCTTGGCTGAACTGTGATCCAAATCCTCCTGATATTTACTGCATTGGATTCCAAGAGCTGGACTTGAGC
  ACAGAAGCCTTTTTCTACTTTGAGTCTGTAAAAGAGCAAGAATGGGCCATGGCTGTGGAAAGGGGTCTGC
  CTTCGAAGGCCAAGTATAAAAAGGTTCAACTGGTCCGCCTTGTGGGGATGATGCTTCTCGTATTTGCCAA
  AAAAGATCAGTGTCAATATATCCGAGATATTGCTACAGAAACAGTCGGAACAGGAATCATGGGGAAAATG
  GGAAACAAAGGTGGAGTAGCTATGAGATTTGTGTTCCACAACACCACTTTCTGCATTGTCAATTCCCACC
  TGGCTGCCCACGTGGAAGAGTTTGAACGAAGGAACCAGGATTATAAAGACATCTGTGCGAGAATGAGCTT
  TTCAGTCCCCAATCAGACTCTCCCACAAGTGAACATCATGAAGCATGATGTTGTCATTTGGTTGGGAGAC
  TTGAACTACAGACTTTGCATGCCTGATGCCAATGAGGTGAAAAGTCTTATTAATAAAAATGAGCTTCAGA
  AGCTGTTGAAATTCGACCAGTTAAACATTCAGCGCACACAGAAAAAAGCTTTTGTGGATTTCAATGAAGG
  GGAAATCAAGTTTATTCCCACTTACAAGTATGATTCTAAAACTGACAGATGGGATTCCAGTGGGAAATGC
  CGAGTCCCAGCCTGGTGTGACCGAATTCTTTGGAGAGGAATAAATGTTAATCAACTTCATTACCGGAGTC
  ACATGGAACTCAAAACTAGTGACCACAAACCTGTTAGCGCCCTGTTCCATATTGGGGTGAAGGTTGTAGA
  TGAACGGCGGTATCGGAAGGTCTTTGAAGATATTGTACGCATTATGGACAGAATGGAAAATGACTTCCTT
  CCTTCATTAGACCTTAGCAGGAGAGAGTTTATGTTTGAGAATGTGAAGTTTCGGCAGCTGCAAAAGGAGA
  AGTTCCAGATCAGCAACAATGGACAGGTTCCCTGCCATTTTTCTTTCATCCCTAAGCTTAATGACACCCA
  ATACTGCAAGCCATGGCTTCGAGCTGAACCTTTTGAGGGCTACTTGGAGCCAAACGAGACAATAGACATT
  TCCCTTGATGTATACGTCAGCAAAGACTCTGTAACCATCCTGAACTCTGGTGAAGATAAGATTGAAGATA
  TTCTTGTCCTCCATTTGGATCGAGGAAAAGATTACTTCTTGACCATCAGTGGGAATTACCTTCCAAGTTG
  CTTTGGAACCTCATTGGAGGCTTTGTGCCGAATGAAAAGACCAATCCGAGAAGTTCCTGTCACCAAACTC
  ATAGACTTGGAAGAAGACAGCTTCCTAGAAAAGGAGAAATCCCTTCTGCAGATGGTCCCCTTGGATGAAG
  GTACCAGTGAGCGACCCCTTCAAGTCCCCAAAGAGATCTGGCTTCTAGTAGATCACTTGTTCAAATATGC
  ATGTCACCAGGAGGACTTGTTCCAAACCCCTGGAATGCAGGAGGAGTTACAGCAGATCATTGATTGTCTG
  GATACCAGCATTCCTGAGACAATCCCTGGTAGTAACCATTCTGTGGCTGAAGCACTGCTCATTTTCCTGG
  AAGCCCTGCCAGAGCCAGTCATCTGTTATGAGCTGTATCAGCGATGTCTCGACTCTGCTCATGATCCTCG
  GATCTGCAAACAGGTCATTTCCCAGCTTCCAAGGTGCCATAGAAATGTTTTCCGCTACTTGATGGCATTC
  CTTCGAGAACTCTTAAAATTCTCTGATTACAACAATGTCAGCACCAACATGATCGCTACTCTGTTCACTA
  GCCTTCTCCTAAGGCCTCCACCAAACCTCATGGCAAGACAGACTCCAAGTGACCGCCAGCGCGCCATCCA
  GTTTCTTCTAGTCTTCCTGCTTGGGAGCGAGGAAGACTAA
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_001108256
• ORF Size: 2700 bp
• Insert Size: 2700
• 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_001108256.2, NP_001101726.2
• RefSeq Size: 5157
• RefSeq ORF: 2700
• Locus ID: 317576
• Gene Summary: mutation in human OCRL causes Lowe syndrome, also known as oculocerebrorenal syndrome; mouse homolog RIKEN cDNA 9530014D17 possesses an inositol polyphosphate phosphatase domain [RGD, Feb 2006]