VGLUT3 (SLC17A8) (NM_139319) Human Untagged Clone

CAT#: SC306142

SLC17A8 (untagged)-Human solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 (SLC17A8), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SLC17A8
• Synonyms: DFNA25; VGLUT3
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_139319, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCCTTTTAAAGCATTTGATACCTTCAAAGAAAAAATTCTGAAACCTGGGAAGGAAGGAGTGAAGAACG
  CCGTGGGAGATTCTTTGGGAATTTTACAAAGAAAAATCGATGGGACAACTGAGGAAGAAGATAACATTGA
  GCTGAATGAAGAAGGAAGGCCGGTGCAGACGTCCAGGCCAAGCCCCCCACTCTGCGACTGCCACTGCTGC
  GGCCTCCCCAAGCGTTACATCATTGCTATCATGAGTGGGCTGGGATTCTGCATTTCCTTTGGGATCCGGT
  GCAATCTTGGAGTTGCCATTGTGGAAATGGTCAACAATAGCACCGTATATGTTGATGGAAAACCGGAAAT
  TCAGACAGCACAGTTTAACTGGGATCCAGAAACAGTGGGCCTTATCCATGGATCTTTTTTCTGGGGCTAT
  ATTATGACACAAATTCCAGGTGGTTTCATTTCAAACAAGTTTGCTGCTAACAGGGTCTTTGGAGCTGCCA
  TCTTCTTAACATCGACTCTGAACATGTTTATTCCCTCTGCAGCCAGAGTGCATTACGGATGCGTCATGTG
  TGTCAGAATTCTGCAAGGTTTAGTGGAGGGTGTGACCTACCCAGCCTGCCATGGGATGTGGAGTAAGTGG
  GCACCACCTTTGGAGAGAAGCCGACTGGCCACAACCTCTTTTTGTGGTTCCTATGCAGGGGCAGTGGTTG
  CCATGCCCCTGGCTGGGGTGTTGGTGCAGTACATTGGATGGTCCTCTGTCTTTTATATTTATGGCATGTT
  TGGGATTATTTGGTACATGTTTTGGCTGTTGCAGGCCTATGAGTGCCCAGCAGCTCATCCAACAATATCC
  AATGAGGAGAAGACCTATATAGAGACAAGCATAGGAGAGGGGGCCAACGTGGTTAGTCTAAGTAAATTTA
  GTACCCCATGGAAAAGATTTTTCACATCTTTGCCGGTTTATGCAATCATTGTGGCAAATTTTTGCAGAAG
  CTGGACCTTTTATTTGCTCCTCATAAGTCAGCCTGCTTATTTTGAAGAGGTCTTTGGATTTGCAATAAGT
  AAGGTGGGTCTCTTGTCAGCAGTCCCACACATGGTTATGACAATCGTTGTACCTATTGGAGGACAATTGG
  CTGATTATTTAAGAAGCAGACAAATTTTAACCACAACTGCTGTCAGAAAAATCATGAACTGTGGAGGTTT
  TGGCATGGAGGCAACCTTACTCCTGGTGGTTGGCTTTTCGCATACCAAAGGGGTGGCTATCTCCTTTCTG
  GTACTTGCTGTAGGATTTAGTGGCTTCGCTATTTCAGGTTTTAATGTCAACCACCTGGACATTGCCCCAC
  GCTATGCCAGCATTCTCATGGGGATCTCAAACGGAGTGGGAACCCTCTCTGGAATGGTCTGTCCCCTCAT
  TGTCGGTGCAATGACCAGGCACAAGACCCGTGAAGAATGGCAGAATGTGTTCCTCATAGCTGCCCTGGTG
  CATTACAGTGGTGTGATCTTCTATGGGGTCTTTGCTTCTGGGGAGAAACAGGAGTGGGCTGACCCAGAGA
  ATCTCTCTGAGGAGAAATGTGGAATCATTGACCAGGACGAATTAGCTGAGGAGATAGAACTCAACCATGA
  GAGTTTTGCGAGTCCCAAAAAGAAGATGTCTTATGGAGCCACCTCCCAGAATTGTGAAGTCCAGAAGAAG
  GAATGGAAAGGACAGAGAGGAGCGACCCTTGATGAGGAAGAGCTGACATCCTACCAGAATGAAGAGAGAA
  ACTTCTCAACTATATCCTAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_139319
• ORF Size: 1770 bp
• OTI Disclaimer: Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.
  
  The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• 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_139319.2, NP_647480.1
• RefSeq Size: 3983
• RefSeq ORF: 1770
• Locus ID: 246213
• Protein Families: Transmembrane
• Gene Summary: This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
  Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).