SNX2 (NM_003100) Human Untagged Clone

CAT#: SC118155

SNX2 (untagged)-Human sorting nexin 2 (SNX2)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SNX2
• Synonyms: TRG-9
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC118155 sequence for NM_003100 edited (data generated by NextGen Sequencing)
  ATGGCGGCCGAGAGGGAACCTCCTCCGCTGGGGGACGGGAAGCCCACCGACTTTGAGGAT
  CTGGAGGACGGAGAGGACCTGTTCACCAGCACTGTCTCCACCCTAGAGTCAAGTCCATCA
  TCTCCAGAACCAGCTAGTCTTCCTGCAGAAGATATTAGTGCAAACTCCAATGGCCCAAAA
  CCCACAGAAGTTGTATTAGATGATGACAGAGAAGATCTTTTTGCAGAAGCCACAGAAGAA
  GTTTCTTTGGACAGCCCTGAAAGGGAACCTATCCTATCCTCGGAACCTTCTCCTGCAGTC
  ACACCTGTCACTCCTACTACACTCATTGCTCCTAGAATTGAATCAAAGAGTATGTCTGCT
  CCCGTGATCTTTGATAGATCCAGGGAAGAGATTGAAGAAGAAGCAAATGGAGACATTTTT
  GACATAGAAATTGGTGTATCAGATCCAGAAAAAGTTGGTGATGGCATGAATGCCTATATG
  GCATATAGAGTAACAACAAAGACATCTCTTTCCATGTTCAGTAAGAGTGAATTTTCAGTG
  AAAAGAAGATTCAGCGACTTTCTTGGTTTGCACAGCAAATTAGCAAGCAAATATTTACAT
  GTTGGTTATATTGTGCCACCAGCTCCAGAAAAGAGTATAGTAGGGATGACCAAGGTCAAA
  GTGGGTAAAGAAGACTCATCATCCACTGAGTTTGTAGAAAAACGGAGAGCAGCTCTTGAA
  AGGTATCTTCAAAGAACAGTAAAACATCCAACTTTACTACAGGATCCTGATTTAAGGCAG
  TTCTTGGAAAGTTCAGAGCTGCCTAGAGCAGTTAATACACAGGCTCTGAGTGGAGCAGGA
  ATATTGAGGATGGTGAACAAGGCTGCCGACGCTGTCAACAAAATGACAATCAAGATGAAT
  GAATCGGATGCATGGTTTGAAGAAAAGCAGCAGCAATTTGAGAATCTGGATCAGCAACTT
  AGGAAACTTCATGTCAGTGTTGAAGCCTTGGTCTGTCATAGAAAAGAACTTTCAGCCAAC
  ACAGCTGCCTTTGCTAAAAGTGCTGCCATGTTAGGTAATTCTGAGGATCATACTGCTTTA
  TCTAGAGCTTTGTCTCAGCTTGCAGAGGTTGAGGAGAAGATAGACCAGTTACATCAAGAA
  CAAGCTTTTGCTGACTTTTATATGTTTTCAGAACTACTTAGTGACTACATTCGTCTTATT
  GCTGCAGTGAAAGGTGTGTTTGACCATCGAATGAAGTGCTGGCAGAAATGGGAAGATGCT
  CAAATTACTTTGCTCAAAAAACGTGAAGCTGAAGCAAAAATGATGGTTGCTAACAAACCA
  GATAAAATACAGCAAGCTAAAAATGAAATAAGAGAGTGGGAGGCGAAAGTGCAACAAGGG
  GAAAGAGATTTTGAACAGATATCTAAAACGATTCGAAAAGAAGTGGGAAGATTTGAGAAA
  GAACGAGTGAAGGATTTTAAAACCGTTATCATCAAGTACTTAGAATCACTAGTTCAAACA
  CAACAACAGCTGATAAAATACTGGGAAGCATTCCTACCTGAAGCCAAAGCCATTGCCTAG
  
  Clone variation with respect to NM_003100.2
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_003100 unedited
  AAGCCAGATATTGTAATACGACTTACTATAGGGCGGCCGCGCAATTCGCACGAGGCGAAG
  AGGCGGCCGAGAGGGAACCTCCTCCGCTGGGGGACGGGAAGCCCACCGACTTTGAGGATC
  TGGAGGACGGAGAGGACCTGTTCACCAGCACTGTCTCCACCCTAGAGTCAAGTCCATCAT
  CTCCAGAACCAGCTAGTCTTCCTGCAGAAGATATTAGTGCAAACTCCAATGGCCCAAAAC
  CCACAGAAGTTGTATTAGATGATGACAGAGAAGATCTTTTTGCAGAAGCCACAGAAGAAG
  TTTCTTTGGACAGCCCTGAAAGGGAACCTATCCTATCCTCGGAACCTTCTCCTGCAGTCA
  CACCTGTCACTCCTACTACACTCATTGCTCCTAGAATTGAATCAAAGAGTATGTCTGCTC
  CCGTGATCTTTGATAGATCCAGGGAAGAGATTGAAGAAGAAGCAAATGGAGACATTTTTG
  ACATAGAAATTGGTGTATCAGATCCAGAAAAAGTTGGTGATGGCATGAATGCCTATATGG
  CATATAGAGTAACAACAAAGACATCTCTTTCCATGTTCAGTAAGAGTGAATTTTCAGTGA
  AAAGAAGATTCAGCGACTTTCTTGGTTTGCACAGCAAATTAGCAAGCAAATATTTACATG
  TTGGTTATATTGTGCCACCAGCTCCAGAAAAGAGTATAGTAGGGATGACCAAGGTCAAAG
  TGGGTAAAGAAGACTCATCATCCACTGAGTTTGTAGAAAAACGGAGAGCAGCTCTTGAAA
  GGTATCTTCAAAGAACAGTAAAACATCCAACTTTACTACAGGATCCTGATTTAAGGCAGT
  TCTTGGNAAGTTCAGAGCTGCCTAGAGCAGTTAATACACAGGCTCTGAGTGGAGCANNGA
  TATTGAAGATGGTGAACA
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_003100 unedited
  NACTTTAGCTCTGNACCGCGCCNCGCATNCTAGNATCGAGTTTTTTTTTTTTTTTTTTCA
  CAGGAAATATCATTTTATTACTGTAATCACAAAATCGTAATTTCTGTACAGGAATGTATA
  AGTGAACATTATTCAAAGCATTGGTAATTCACTTCATAAAGAGGGTAAACATACTACAGA
  ACATATTGTAAAGAAAAAATATTGCAAAATTTTCTGGTCTTGCAGTGCACTATTTAGTGC
  AAGTATTTAAGACACAATAGTGTTCAATTCAGCAAAGTATTGCAGAATGTCATGCCACAG
  TCCACTTAATTCAAAGAGGGTCAGGACATGCAGCTTGTAATAAAATGTCACAGTGTGTGT
  GTGTGTGTGTGCGTGTGCGTGTATATAAAACCACCATGTAATTCATAAAATATATAGTGG
  TTTATTTAGATGGCTTTAAATGATTTCACTGTGGAATCCAGCATAACTGGAACAACATCC
  AAGGTCTTCTTAACGGCAACAATCTTATTGCTAGGCAATGGCTTTGGCTTCAGGCACGAA
  TGCTTCCCAGTATTTTATCAGCTGTCGTTGTGCCCGAACTAGTGATTCTAACTACTTGAT
  GATAACGGTTTTAAAATCCTTCACTCGTTCTTTCTAAAATCTTCCCACTTCTTTTCAAAA
  CGCTTTAGATATCCGTCCAAAATCTCTTTCCCCTTGTTGCACTTTCGCCTTCCACTCTTT
  TATTTAATTTTTAGCTCGCCGCACTTCACTCGGCTTGGAACCCACCATTATTTTTGCTCC
  CACTTCCAGTCTTTTGAACAAAGAATTTGAGCCTGTTCCCTTTGCTGCCAGACTTTATTC
  CACGGTCACACACACCTTAACTGCAGCAATAAGACAAATGCGTCTCTAACACATTCTGAA
  CA
  
• Restriction Sites: NotI-NotI
• ACCN: NM_003100
• Insert Size: 2100 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).
• Product Components: The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
• Reconstitution: 1. Centrifuge at 5,000xg for 5min.
  2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
  3. Close the tube and incubate for 10 minutes at room temperature.
  4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
  5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.

Reference Data

• RefSeq: NM_003100.2, NP_003091.2
• RefSeq Size: 2091 bp
• RefSeq ORF: 1560 bp
• Locus ID: 6643
• UniProt ID: O60749
• Cytogenetics: 5q23.2
• Domains: PX, Sorting_nexin
• Gene Summary: This gene belongs to the sorting nexin family whose members contain the phosphoinositide-binding phox (PX) domain. The encoded protein is a component of the retromer complex which plays a role in protein sorting in the endocytic pathway. This protein may form oligomeric complexes with other family members. Alternate splicing results in multiple transcript variants of this gene. Pseudogenes associated with this gene are located on chromosomes 1 and 7. [provided by RefSeq, May 2013]
  Transcript Variant: This variant (1) represents the shorter transcript and encodes the longer 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.