PREPL (NM_001171613) Human Untagged Clone

CAT#: SC329016

PREPL (untagged)-Human prolyl endopeptidase-like (PREPL) transcript variant 6

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: PREPL
• Synonyms: CMS22
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001171613, the custom clone sequence may differ by one or more nucleotides
  ATGGATGCATTTGAAAAAGTGAGAACAAAATTAGAAACACAGCCACAAGAAGAATATGAA
  ATCATCAATGTGGAAGTTAAACATGGTGGTTTTGTTTATTACCAAGAAGGTTGTTGCTTG
  GTTCGTTCCAAAGATGAAGAAGCAGACAATGATAATTATGAAGTTTTATTCAATTTGGAG
  GAACTTAAGTTAGACCAGCCCTTCATTGATTGTATCAGAGTTGCTCCAGATGAAAAATAT
  GTGGCTGCCAAGATAAGAACTGAAGATTCTGAAGCATCTACCTGTGTAATTATAAAGCTC
  AGCGATCAGCCCGTAATGGAAGCTTCTTTCCCGAATGTGTCCAGTTTTGAATGGGTAAAG
  GACGAGGAAGATGAAGATGTTTTATTCTACACCTTCCAGAGGAACCTTCGCTGTCATGAC
  GTATATCGAGCCACTTTTGGTGATAACAAACGTAATGAACGCTTTTACACAGAAAAAGAC
  CCAAGCTACTTTGTTTTCCTTTATCTTACAAAAGACAGTCGTTTCCTCACCATAAATATT
  ATGAACAAGACTACTTCTGAAGTGTGGTTGATAGATGGCCTGAGCCCTTGGGACCCACCA
  GTACTTATCCAGAAGCGAATACATGGGGTCCTTTACTATGTTGAACACAGAGATGATGAA
  TTATACATTCTCACTAATGTTGGAGAACCTACAGAATTTAAGCTAATGAGAACAGCGGCT
  GATACCCCTGCAATTATGAATTGGGATTTATTTTTTACAATGAAGAGAAATACAAAAGTG
  ATAGACTTGGACATGTTTAAGGATCACTGTGTTCTATTTCTGAAGCACAGCAATCTCCTT
  TATGTTAATGTGATTGGTCTGGCTGATGATTCAGTTCGGTCTCTAAAGCTCCCTCCTTGG
  GCCTGTGGATTCATAATGGATACAAATTCTGACCCAAAGAACTGCCCCTTTCAACTTTGC
  TCTCCAATACGTCCCCCAAAATATTACACATACAAGTTTGCAGAAGGCAAACTGTTTGAG
  GAAACTGGGCATGAAGACCCAATCACAAAGACTAGTCGCGTTTTACGTCTAGAAGCCAAA
  AGCAAGGATGGAAAATTAGTGCCAATGACTGTTTTCCACAAAACTGACTCTGAGGACTTG
  CAGAAGAAACCTCTCTTGGTACATGTATATGGAGCTTATGGAATGGATTTGAAAATGAAT
  TTCAGGCCTGAGAGGCGGGTCCTGGTGGATGATGGATGGATATTAGCATACTGCCATGTT
  CGAGGTGGTGGTGAGTTAGGCCTCCAGTGGCACGCTGATGGCCGCCTAACTAAAAAACTC
  AATGGCCTTGCTGATTTAGAGGCTTGCATTAAGACGCTTCATGGCCAAGGCTTTTCTCAG
  CCAAGTCTAACAACCCTGACTGCTTTCAGTGCTGGAGGGGTGCTTGCAGGAGCATTGTGT
  AATTCTAATCCAGAGCTGGTGAGAGCGGTGACTTTGGAGGCACCTTTCTTGGATGTTCTC
  AACACCATGATGGACACTACACTTCCTCTGACATTAGAAGAATTAGAAGAATGGGGGAAT
  CCTTCATCTGATGAAAAACACAAGAACTACATAAAACGTTACTGTCCCTATCAAAATATT
  AAACCTCAGCATTATCCTTCAATTCACATAACGGCATATGAAAACGATGAACGGGTACCT
  CTGAAAGGAATTGTAAGTTATACTGAGAAACTCAAGGAAGCCATCGCGGAGCATGCTAAG
  GACACAGGTGAAGGCTATCAGACCCCTAATATTATTCTAGATATTCAGCCTGGAGGCAAT
  CATGTAATTGAGGATTCTCACAAAAAGATTACAGCCCAAATTAAATTCCTGTACGAGGAA
  CTTGGACTTGACAGCACCAGTGTTTTCGAGGATCTTAAGAAATACCTGAAATTCTGA
  
• Restriction Sites: Please inquire
• ACCN: NM_001171613
• ORF Size: 1917 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_001171613.1, NP_001165084.1
• RefSeq Size: 5907
• RefSeq ORF: 1917
• Locus ID: 9581
• Protein Families: Druggable Genome, Protease
• Gene Summary: The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene. [provided by RefSeq, Jan 2010]
  Transcript Variant: This variant (6) contains an alternate exon at the 5' end compared to variant 1, resulting in translation initiation from an in-frame downstream AUG and a shorter isoform (4) compared to isoform 1. Variants 6 and 7 encode the same isoform. 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.