PARD3 (NM_001184791) Human Untagged Clone

CAT#: SC329318

PARD3 (untagged)-Human par-3 partitioning defective 3 homolog (C. elegans) (PARD3) transcript variant 8

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: PARD3
• Synonyms: ASIP; Baz; PAR3; PAR3alpha; PARD-3; PARD3A; PPP1R118; SE2-5L16; SE2-5LT1; SE2-5T2
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001184791, the custom clone sequence may differ by one or more nucleotides
  ATGAAAGTGACCGTGTGCTTCGGACGGACCCGGGTGGTCGTGCCGTGCGGGGACGGCCAC
  ATGAAAGTTTTCAGCCTCATCCAGCAGGCGGTGACCCGCTACCGGAAGGCCATCGCCAAG
  GATCCAAACTACTGGATACAGGTGCATCGCTTGGAACATGGAGATGGAGGAATACTAGAC
  CTTGATGACATTCTTTGTGATGTAGCAGACGATAAAGACAGACTGGTAGCAGTGTTTGAT
  GAGCAGGATCCACATCACGGAGGTGATGGCACCAGTGCCAGTTCCACGGGTACCCAGAGC
  CCAGAGATATTTGGTAGTGAGCTTGGCACCAACAATGTCTCAGCCTTTCAGCCTTACCAA
  GCAACAAGTGAAATTGAGGTCACACCTTCAGTCCTTCGAGCAAATATGCCTCTTCATGTT
  CGACGCAGTAGTGACCCAGCTCTAATTGGCCTCTCCACTTCTGTCAGTGATAGTAATTTT
  TCCTCTGAAGAGCCTTCAAGGAAAAATCCCACACGCTGGTCAACAACAGCTGGCTTCCTC
  AAGCAGAACACTGCTGGGAGTCCTAAAACCTGCGACAGGAAGGATGAGGATGGGACAGAA
  GAGGATAACAGTCGTGTTGAACCTGTTGGACATGCTGACACGGGTTTGGAGCATATACCC
  AACTTTTCTCTGGATGATATGGTAAAGCTCGTAGAAGTCCCCAACGATGGAGGGCCTCTG
  GGAATCCATGTAGTGCCTTTCAGTGCTCGAGGCGGCAGAACCCTGGGGTTATTAGTAAAA
  CGATTGGAGAAAGGTGGTAAAGCTGAACATGAAAATCTTTTTCGTGAGAATGATTGCATT
  GTCAGGATTAATGATGGCGACCTTCGAAATAGAAGATTTGAACAAGCACAACATATGTTT
  CGCCAAGCCATGCGTACACCCATCATTTGGTTCCATGTGGTTCCTGCAGCAAATAAAGAG
  CAGTATGAACAACTATCCCAAAGTGAGAAGAACAATTACTATTCAAGCCGTTTTAGCCCT
  GACAGCCAGTATATTGACAACAGGAGTGTGAACAGTGCAGGGCTTCACACGGTGCAGAGA
  GCACCCCGACTGAACCACCCGCCTGAGCAGATAGACTCTCACTCAAGACTACCTCATAGC
  GCACACCCCTCGGGAAAACCACCATCCGCTCCAGCCTCGGCACCTCAGAATGTATTTAGT
  ACGACTGTAAGCAGTGGTTATAACACCAAAAAAATAGGCAAGAGGCTTAATATCCAGCTT
  AAGAAAGGTACAGAAGGTTTGGGATTCAGCATCACTTCCAGAGATGTAACAATAGGTGGC
  TCAGCTCCAATCTATGTGAAAAACATTCTCCCCCGGGGGGCGGCCATTCAGGATGGCCGA
  CTTAAGGCAGGAGACAGACTTATAGAGGTAAATGGAGTAGATTTAGTGGGCAAATCCCAA
  GAGGAAGTTGTTTCGCTGTTGAGAAGCACCAAGATGGAAGGAACTGTGAGCCTTCTGGTC
  TTTCGCCAGGAAGACGCCTTCCACCCAAGGGAACTGAAAGCAGAAGATGAGGATATTGTT
  CTTACACCTGATGGCACCAGGGAATTTCTGACATTTGAAGTCCCACTTAATGATTCAGGA
  TCTGCAGGCCTTGGTGTCAGTGTCAAAGGTAACCGGTCAAAAGAGAACCACGCAGATTTG
  GGAATCTTTGTCAAGTCCATTATTAATGGAGGAGCAGCATCTAAAGATGGAAGGCTTCGG
  GTGAATGATCAACTGATAGCAGTAAATGGAGAATCCCTGTTGGGCAAGACAAACCAAGAT
  GCCATGGAAACCCTAAGAAGGTCTATGTCTACTGAAGGCAATAAACGAGGAATGATCCAG
  CTTATTGTTGCAAGGAGAATAAGCAAGTGCAATGAGCTGAAGTCACCTGGGAGCCCCCCT
  GGACCTGAGCTGCCCATTGAAACAGCGTTGGATGATAGAGAACGAAGAATTTCCCATTCC
  CTCTACAGTGGGATTGAGGGGCTTGATGAATCGCCCAGCAGAAATGCTGCCCTCAGTAGG
  ATAATGGGTAAATACCAGCTGTCCCCTACAGTGAATATGCCCCAAGATGACACTGTCATT
  ATAGAAGATGACAGGTTGCCAGTGCTTCCTCCACATCTCTCTGACCAGTCCTCTTCCAGC
  TCCCATGATGATGTGGGGTTTGTGACGGCAGATGCTGGTACTTGGGCCAAGGCTGCAATC
  AGTGATTCAGCCGACTGCTCTTTGAGTCCAGATGTTGATCCAGTTCTTGCTTTTCAACGA
  GAAGGATTTGGACGTCAGAGTATGTCAGAAAAACGCACAAAGCAATTTTCAGATGCCAGT
  CAATTGGATTTCGTTAAAACACGAAAATCAAAAAGCATGGATTTAGGTAGTTCTCCCAGC
  AGAGATGTGGGTCCTTCCCTGGGTCTGAAGAAGTCAAGCTCGTTGGAGAGTCTGCAGACC
  GCAGTTGCCGAGGTGACTTTGAATGGGGATATTCCTTTCCATCGTCCACGGCCGCGGATA
  ATCAGAGGCAGGGGATGCAATGAGAGCTTCAGAGCTGCCATCGACAAATCTTATGATAAA
  CCCGCGGTAGATGATGATGATGAAGGCATGGAGACCTTGGAAGAAGACACAGAAGAAAGT
  TCAAGATCAGGGAGAGAGTCTGTATCCACAGCCAGTGATCAGCCTTCCCACTCTCTGGAG
  AGACAAATGAATGGAAACCAAGAGAAAGGTGATAAGACTGATAGAAAAAAGGATAAAACT
  GGAAAAGAAAAGAAGAAAGATAGAGATAAGGAGAAGGATAAAATGAAAGCCAAGAAGGGA
  ATGCTGAAGGGCTTGGGAGACATGTTCAGGATTCAAGCCAAAACTCGAGAATTTAGGGAA
  CGACAAGCTCGAGAGCGTGACTATGCTGAAATTCAAGATTTTCATCGGACATTTGGCTGT
  GATGATGAGTTAATGTATGGGGGAGTTTCTTCTTATGAAGGTTCCATGGCTCTCAACGCT
  AGACCTCAGAGCCCACGAGAAGGGCATATGATGGATGCTTTGTATGCCCAAGTCAAGAAG
  CCGCGGAATTCCAAACCCTCACCTGTAGACAGTAACAGATCAACTCCTAGCAATCATGAT
  CGGATACAGCGTCTGAGGCAAGAATTTCAGCAAGCAAAGCAAGATGAAGATGTAGAAGAT
  CGTCGGCGGACCTATAGTTTTGAGCAACCCTGGCCGAACGCACGGCCGGCGACGCAGAGC
  GGGCGACACTCGGTGTCCGTGGAGGTGCAGATGCAGCGGCAGCGGCAGGAGGAGCGCGAG
  AGCTCCCAGCAGGCCCAGCGCCAGTACAGCTCTCTGCCTCGGCAAAGCAGGAAAAATGCC
  AGCTCGGTCTCCCAGGACTCTTGGGAGCAGAACTACTCCCCTGGGGAAGGCTTCCAGAGT
  GCCAAAGAGAACCCCAGGTACTCCAGCTACCAAGGCTCCAGGAACGGCTACCTGGGAGGA
  CATGGCTTCAACGCCAGGGTCATGCTGGAAACTCAGGAGCTCCTTCGCCAGGAACAGAGG
  CGGAAGGAGCAGCAGATGAAGAAGCAGCCTCCTTCCGAGGGGCCCAGCAACTATGACTCG
  TATAAGAAAGTCCAGGACCCCAGTTACGCCCCTCCCAAGGGGCCCTTCCGGCAAGATGTG
  CCCCCCTCCCCTTCTCAGGTTGCGAGGCTGAACAGACTTCAGACTCCTGAGAAAGGGAGG
  CCCTTCTATTCCTGA
  
• Restriction Sites: Please inquire
• ACCN: NM_001184791
• ORF Size: 3735 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_001184791.1, NP_001171720.1
• RefSeq Size: 5677
• RefSeq ORF: 3735
• Locus ID: 56288
• Protein Pathways: Adherens junction, Chemokine signaling pathway, Endocytosis, Neuroactive ligand-receptor interaction, Tight junction
• Gene Summary: This gene encodes a member of the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]
  Transcript Variant: This variant (8) lacks four alternate, in-frame segments and uses a different splice site, in the coding region, compared to variant 1. The resulting protein (isoform 8) is shorter when it is compared to isoform 1. This variant has also been called 'variant e'. 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.