Synaptojanin 2 (SYNJ2) (NM_001178088) Human Untagged Clone

CAT#: SC329322

SYNJ2 (untagged)-Human synaptojanin 2 (SYNJ2) transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SYNJ2
• Synonyms: INPP5H
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001178088, the custom clone sequence may differ by one or more nucleotides
  ATGATTTACATGGACGATGGAGTGTCATCTTTTGTCCAGATCAGAGGCTCCGTTCCGCTG
  TTCTGGGAACAGCCAGGGCTTCAGGTTGGCTCCCATCATCTGAGACTCCACAGAGGCCTG
  GAAGCCAATGCCCCTGCTTTCGACAGGCACATGGTGCTTCTGAAGGAGCAGTACGGGCAG
  CAGGTGGTCGTGAACCTTCTGGGAAGCAGAGGCGGAGAGGAGGTGCTCAACAGAGCCTTC
  AAGAAGCTGCTCTGGGCTTCTTGCCACGCGGGCGACACGCCTATGATCAATTTTGACTTC
  CATCAGTTTGCCAAAGGTGGGAAGCTAGAGAAATTGGAGACCCTCTTGAGGCCACAGTTA
  AAGCTGCACTGGGAAGACTTCGATGTGTTCACAAAGGGGGAGAACGTCAGTCCACGTTTT
  CAGAAAGGCACTTTGCGGATGAACTGTCTTGACTGCCTGGACCGAACCAACACTGTGCAG
  AGCTTCATCGCGCTCGAGGTCCTGCATCTGCAGCTCAAGACCCTGGGGCTGAGTTCAAAA
  CCCATCGTTGACCGCTTTGTGGAGTCCTTCAAAGCCATGTGGTCTCTGAATGGCCACAGC
  CTGAGCAAGGTGTTCACAGGCAGCAGAGCCCTGGAAGGGAAGGCCAAGGTGGGGAAGCTG
  AAGGATGGAGCCCGGTCCATGTCTCGAACCATCCAGTCCAACTTCTTCGACGGGGTGAAG
  CAGGAGGCCATCAAGCTGCTGCTGGTTGGGGACGTCTACGGCGAGGAGGTGGCAGACAAA
  GGGGGCATGCTGCTGGACAGCACGGCGCTCCTGGTGACTCCCAGGATCCTGAAAGCTATG
  ACTGAGCGTCAGTCCGAATTCACAAATTTCAAGCGGATCCGGATTGCTATGGGGACCTGG
  AACGTGAACGGAGGAAAGCAGTTCCGGAGCAACGTGCTCAGGACGGCGGAGCTGACAGAC
  TGGCTGCTCGACTCGCCCCAGCTCTCGGGAGCTACCGACTCCCAGGATGACAGCAGCCCA
  GCTGACATATTTGCTGTGGGGTTTGAAGAGATGGTGGAATTGAGCGCAGGGAATATTGTC
  AATGCCAGTACTACCAACAAGAAGATGTGGGGTGAACAGCTTCAGAAAGCCATCTCACGC
  TCTCATAGATACATTCTGTTGACTTCGGCACAGCTGGTGGGCGTCTGTCTTTATATCTTT
  GTACGTCCATACCATGTCCCGTTCATCAGGGACGTAGCCATCGACACAGTGAAGACGGGC
  ATGGGGGGCAAGGCGGGGAACAAGGGCGCCGTCGGCATCCGCTTCCAGTTCCACAGCACC
  AGCTTCTGCTTCATATGTAGTCACCTGACGGCCGGGCAGTCCCAGGTGAAGGAGCGGAAT
  GAAGACTACAAGGAGATCACCCAGAAACTCTGCTTCCCAATGGGGAGAAATGTTTTTTCT
  CATGATTATGTATTTTGGTGTGGCGATTTCAACTACCGCATTGATCTTACTTATGAAGAA
  GTCTTCTATTTTGTTAAACGCCAAGACTGGAAGAAACTTCTGGAATTTGATCAACTACAG
  CTACAGAAATCAAGTGGAAAAATTTTTAAGGACTTTCACGAAGGAGCCATTAACTTTGGA
  CCCACCTACAAGTATGACGTTGGCTCAGCCGCCTACGATACAAGCGACAAATGCCGCACC
  CCCGCCTGGACAGACAGGGTGCTGTGGTGGAGGAAGAAACATCCCTTTGATAAAACAGCT
  GGAGAACTCAACCTTCTAGACAGTGATCTAGATGTTGACACCAAAGTCAGACACACCTGG
  TCTCCTGGTGCCCTGCAGTATTATGGTCGTGCGGAGCTACAAGCGTCTGATCACAGACCT
  GTGCTGGCGATCGTGGAGGTGGAAGTTCAGGAAGTCGATGTGGGTGCTCGGGAGAGGGTT
  TTCCAGGAAGTGTCCTCCTTCCAGGGCCCCCTGGATGCCACTGTTGTAGTAAACCTTCAA
  TCACCGACCTTAGAAGAGAAAAACGAGTTTCCAGAGGACCTGCGTACTGAGCTCATGCAG
  ACCTTGGGGAGTTATGGGACAATTGTTCTTGTCAGGATCAACCAAGGGCAGATGCTGGTA
  ACTTTTGCAGACAGTCACTCGGCTCTCAGTGTCCTGGACGTGGACGGTATGAAGGTGAAA
  GGCAGAGCAGTGAAGATTAGACCGAAGACCAAGGACTGGCTGAAAGGTTTGCGAGAGGAG
  ATCATTCGGAAACGAGACAGCATGGCCCCCGTGTCTCCCACTGCCAACTCCTGTTTGCTG
  GAGGAAAACTTTGACTTCACAAGTTTGGACTATGAGTCAGAAGGGGATATTCTTGAAGAC
  GATGAAGACTACTTGGTGGATGAATTCAATCAGCCTGGAGTCTCGGACAGTGAACTCGGG
  GGAGACGACCTCTCTGATGTCCCCGGCCCCACAGCACTGGCTCCTCCCAGCAAGTCACCT
  GCTCTCACCAAAAAGAAGCAGCATCCAACGTACAAAGATGACGCGGACCTGGTGGAGCTC
  AAGCGGGAGCTGGAAGCCGTCGGGGAGTTCCGCCACCGTTCTCCGAGCAGGTCTCTGTCG
  GTCCCCAACCGGCCTCGGCCACCTCAACCCCCGCAGAGACCCCCCCCTCCAACCGGTTTA
  ATGGTGAAAAAGTCGGCTTCAGATGCGTCCATCTCCTCCGGCACCCATGGACAGTATTCA
  ATTTTGCAGACGGCAAGACTTCTACCAGGAGCACCTCAGCAACCTCCCAAGGCTCGGACT
  GGAATAAGTAAACCTTATAATGTCAAGCAGATCAAAACCACCAATGCCCAGGAGGCAGAA
  GCAGCAATCCGGTGTCTCCTGGAAGCCAGAGGAGGTGCCTCCGAAGAAGCCCTAAGTGCC
  GTGGCCCCAAGGGACCTTGAAGCATCCTCTGAACCAGAGCCCACACCGGGGGCAGCCAAA
  CCAGAGACCCCACAGGCGCCCCCACTCCTTCCCCGTCGGCCCCCACCCAGAGTTCCTGCC
  ATCAAGAAGCCAACCTTGAGAAGGACAGGAAAGCCCCTGTCACCGGAAGAACAGTTTGAG
  CAACAGACTGTCCATTTTACAATCGGGCCCCCGGAGACAAGCGTTGAGGCCCCTCCTGTC
  GTGACAGCCCCTCGAGTCCCTCCTGTTCCCAAACCAAGAACATTTCAGCCTGGGAAAGCT
  GCAGAGAGGCCAAGCCACAGGAAGCCAGCATCAGACGAAGCCCCTCCTGGGGCAGGAGCC
  TCTGTGCCACCACCTCTGGAGGCGCCGCCTCTTGTGCCCAAGGTACCCCCGAGGAGGAAG
  AAGTCAGCCCCCGCAGCCTTCCACCTGCAGGTCCTGCAGAGCAACAGCCAGCTTCTCCAG
  GGCCTCACTTACAATAGCAGTGACAGCCCCTCTGGGCACCCACCTGCCGCGGGCACCGTC
  TTCCCACAAGGGGACTTTCTCAGCACTTCATCTGCTACAAGCCCCGACAGCGATGGCACC
  AAAGCGATGAAGCCAGAGGCAGCCCCACTTCTTGGTGATTATCAGGACCCCTTCTGGAAC
  CTTCTTCACCACCCTAAACTGTTGAATAACACTTGGCTTTCTAAGAGCTCAGACCCTTTG
  GACTCAGGAACCAGGAGCCCCAAAAGAGATCCCATAGACCCAGTGTCAGCTGGCGCTTCA
  GCTGCCAAGGCAGAGCTGCCACCAGATCATGAACACAAAACCTTAGGTCACTGGGTGACA
  ATCAGTGACCAAGAAAAGAGGACAGCACTGCAGGTGTTTGACCCACTGGCAAAAACATGA
  
• Restriction Sites: Please inquire
• ACCN: NM_001178088
• ORF Size: 3780 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_001178088.1, NP_001171559.1
• RefSeq Size: 7339
• RefSeq ORF: 3780
• Locus ID: 8871
• Protein Families: Druggable Genome, Phosphatase
• Protein Pathways: Inositol phosphate metabolism, Metabolic pathways, Phosphatidylinositol signaling system
• Gene Summary: The gene is a member of the inositol-polyphosphate 5-phosphatase family. The encoded protein interacts with the ras-related C3 botulinum toxin substrate 1, which causes translocation of the encoded protein to the plasma membrane where it inhibits clathrin-mediated endocytosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
  Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The resulting protein (isoform 2) has a shorter N-terminus, compared to 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.