SNX17 (NM_014748) Human Untagged Clone

SKU SC114846

SNX17 (untagged)-Human sorting nexin 17 (SNX17)

Product Data

• Type: Human Untagged Clone
• Target Symbol: SNX17
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC114846 sequence for NM_014748 edited (data generated by NextGen Sequencing); ATGCACTTTTCCATTCCCGAAACCGAGTCCCGCAGCGGGGACAGCGGCGGCTCCGCCTAC; GTGGCCTATAACATTCACGTGAATGGAGTCCTGCACTGTCGGGTGCGCTACAGCCAGCTC; CTGGGGCTGCACGAGCAGCTTCGGAAGGAGTATGGGGCCAATGTGCTTCCTGCATTCCCC; CCAAAGAAGCTTTTCTCTCTGACTCCTGCTGAGGTAGAACAGAGGAGAGAGCAGTTAGAG; AAGTACATGCAAGCTGTTCGGCAAGACCCATTGCTTGGGAGCAGCGAGACTTTCAACAGT; TTCCTGCGTCGGGCACAACAGGAGACACAGCAGGTCCCCACAGAGGAAGTGTCCTTGGAA; GTGCTGCTCAGCAACGGGCAGAAAGTTCTGGTCAACGTGCTAACTTCAGATCAGACTGAG; GATGTCCTGGAGGCTGTAGCTGCAAAGCTGGATCTTCCAGATGACTTGATTGGATACTTT; AGTCTATTCTTAGTTCGAGAAAAAGAGGATGGAGCCTTTTCTTTTGTACGGAAGTTGCAA; GAGTTTGAGCTGCCTTATGTGTCTGTCACCAGCCTTCGGAGTCAAGAGTATAAGATTGTG; CTAAGGAAGAGTTATTGGGACTCTGCCTATGATGACGATGTCATGGAGAACCGGGTTGGC; CTGAACCTGCTTTATGCTCAGACGGTATCAGATATTGAGCGTGGGTGGATCTTGGTCACC; AAGGAACAGCACCGGCAACTCAAATCTCTGCAAGAGAAAGTCTCCAAGAAGGAGTTCCTG; AGACTGGCCCAGACGCTGCGGCACTATGGCTACTTGCGCTTTGATGCCTGTGTGGCTGAC; TTCCCAGAAAAGGACTGTCCTGTGGTGGTGAGCGCGGGCAACAGTGAGCTCAGCCTGCAG; CTCCGCCTGCCTGGCCAGCAACTCCGAGAAGGCTCCTTCCGGGTCACCCGCATGCGATGC; TGGCGGGTCACCTCCTCTGTACCATTGCCCAGTGGAAGCACGAGCAGCCCAGGCCGGGGC; CGGGGTGAGGTGCGCCTGGAACTGGCTTTTGAATACCTCATGAGCAAGGACCGGCTACAG; TGGGTCACCATCACTAGCCCCCAGGCTATCATGATGAGCATCTGCTTGCAGTCCATGGTT; GATGAACTGATGGTGAAGAAATCTGGCGGCAGTATCAGGAAGATGCTGCGCCGGCGGGTG; GGGGGTACTCTGAGACGCTCAGACAGCCAGCAAGCAGTGAAGTCCCCACCACTGCTTGAG; TCACCTGATGCCACCCGGGAGTCTATGGTCAAACTCTCAAGTAAGCTGAGTGCCGTGAGC; TTGCGGGGAATTGGCAGTCCCAGCACAGATGCCAGTGCCAGTGATGTCCACGGCAATTTC; GCCTTCGAGGGCATTGGAGATGAGGATCTGTAA; ; Clone variation with respect to NM_014748.2;
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_014748 unedited; NGGTAACGTCATAATTGTAAACGACTCACTATAGGCGGCCGCGNAATTCGCACGAGGCGG; GNGACTCGCTGACAGCGGAGGGGGAGCGTGCAGAGCCGCTGCGGCCCTCACAGTCCGGAG; CCCGGCCGTGCCGTGCCGTAGGGAACATGCACTTTTCCATTCCCGAAACCGAGTCCCGCA; GCGGGGACAGCGGCGGCTCCGCCTACGTGGCCTATAACATTCACGTGAATGGAGTCCTGC; ACTGTCGGGTGCGCTACAGCCAGCTCCTGGGGCTGCACGAGCAGCTTCGGAAGGAGTATG; GGGCCAATGTGCTTCCTGCATTCCCCCCAAAGAAGCTTTTCTCTCTGACTCCTGCTGAGG; TAGAACAGAGGAGAGAGCAGTTAGAGAAGTACATGCAAGCTGTTCGGCAAGACCCATTGC; TTGGGAGCAGCGAGACTTTCAACAGTTTCCTGCGTCGGGCACAACAGGAGACACAGCAGG; TCCCCACAGAGGAAGTGTCCTTGGAAGTGCTGCTCAGCAACGGGCAGAAAGTTCTGGTCA; ACGTGCTAACTTCAGATCAGACTGAGGATGTCCTGGAGGCTGTAGCTGCAAAGCTGGATC; TTCCAGATGACTTGATTGGATACTTTAGTCTATTCTTAGTTCGAGAAAAAGAGGATGGAG; CCTTTTCTTTTGTACGGAAGTTGCAAGAGTTTGAGCTGCCTTATGTGTCTGTCACCAGCC; TTCGGAGTCAAGAGTATAAGATTGTGCTAAGGAAGAGTTATTGGGACTCTGCCTATGATG; ACGATGTCATGGAGAACCGGNNTTGGCCTGACCTGCTTTATGCTCAGACGGTATCAGATA; TTGAGCGTGGGTGGGATCTTGGTCAACCAGGGACAGCACCGGGCAACTCAAAT;
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_014748 unedited; TATGGACCGGCGGCCGCAATCTAGGATCGAGTTTTTTTTTTTTTTTTTTTTTTTTAGGCA; GCAGTCAGGCTGAGTTTAATGATGGGGAACTGGGCCAGACCAAACACAGACCTCTGCCCA; TCCCCTTGGCCTTTGGCCCATGGCTCCAAGAGGCCAGAAGCGGCCCAGAGGGAGATATGG; TTCCTCCCCAAGGCAGGCAGCCATGGTCCCTTAGACTTTGTGCAAAATACTAAATGCTAA; TTTGGCATCGAGGGCCAGCTCTGAAAAGAGAAGGGGCAATCCTCTGTGCAGCCAGCCCAG; GGGACAAGGAAAGGTAGGATACGAGGCCCCTGGCCAAGAGAAAAGGGGTAGGTAGGAAAG; AAGAAGGAAAAGACCCCTCCGCCCCTAGCATGGGGGACACAGGCACAGGGCAAGTTTCTG; TAAATTCCTCTGGGGTAGAGGGCAGACATCCAAGCAGTGGAGATTACAGATCCTCATCTC; CAATGCCCTCGAAGGCGAAATTGCCGTGGACATCACTGGCACTGGCATCTGTGCTGGGAC; TGCCAATTCCCCGCAAGCTCACGGCACTCAGCTTACTTGAGAGTTTGACCATAGACTCCC; GGGTGGCATCAGGTGACTCAAGCAGTGGTGGGGACTTCACTGCTTGCTGGCTGTCTGAGC; GTCTCAAAGTACCCCCCACCCGCCGGCGCAGCATCTTCCTGATACTGCCGNCAGATTTCT; CACCATCAGTTCATCAACCATGGACTGNCAGCAGATGCTCATCATGATAGCCCTGGGGGC; TAGTGATGGTGACCCCACTGTACCCGGGTCCTTGCTCATGAGGTATNTCAAAAGCCAGNT; NCAGNCGCACCTNACCCCCGNCCCNGGNNCTGGCTGTTNGTGCTTTCACTGGGCCATGGA; CAAAAGAAGGGGACCCGCCA;
• Restriction Sites: NotI-NotI
• ACCN: NM_014748
• Insert Size: 2180 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).
• 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 Method: 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.
• Note: Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required.
• Shipping: Ambient

Reference Data

• RefSeq: NM_014748.2, NP_055563.1
• RefSeq Size: 2043 bp
• RefSeq ORF: 1413 bp
• Locus ID: 9784
• UniProt ID: Q15036
• Cytogenetics: 2p23.3
• Domains: PX
• Protein Families: Druggable Genome
• Summary: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a B41 domain. This protein interacts with the cytoplasmic domain of P-selectin, and may function in the intracellular trafficking of P-selectin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012]; Transcript Variant: This variant (1) encodes the longest protein (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.