SLC26A5 (NM_001167962) Human Untagged Clone

CAT#: SC329087

SLC26A5 (untagged)-Human solute carrier family 26 member 5 (prestin) (SLC26A5) transcript variant e

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SLC26A5
• Synonyms: DFNB61; PRES
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001167962, the custom clone sequence may differ by one or more nucleotides
  ATGGATCATGCTGAAGAAAATGAAATCCTTGCAGCAACCCAGAGGTACTATGTGGAAAGG
  CCTATCTTTAGTCATCCGGTCCTCCAGGAAAGACTACACACAAAGGACAAGGTTCCTGAT
  TCCATTGCGGATAAGCTGAAACAGGCATTCACATGTACTCCTAAAAAAATAAGAAATATC
  ATTTATATGTTCCTACCCATAACTAAATGGCTGCCAGCATACAAATTCAAGGAATATGTG
  TTGGGTGACTTGGTCTCAGGCATAAGCACAGGGGTGCTTCAGCTTCCTCAAGGCTTAGCC
  TTTGCAATGCTGGCAGCTGTGCCTCCAATATTTGGCCTGTACTCTTCATTTTACCCTGTT
  ATCATGTATTGTTTTCTTGGAACCTCCAGACACATATCCATAGGTCCTTTTGCTGTTATT
  AGCCTGATGATTGGTGGTGTAGCTGTTCGATTAGTACCAGATGATATAGTCATTCCAGGA
  GGAGTAAATGCAACCAATGGCACAGAGGCCAGAGATGCCTTGAGAGTGAAAGTCGCCATG
  TCTGTGACCTTACTTTCAGGAATCATTCAGTTTTGCCTAGGTGTCTGTAGGTTTGGATTT
  GTGGCCATATATCTCACAGAGCCTCTGGTCCGTGGGTTTACCACCGCAGCAGCTGTGCAT
  GTCTTCACCTCCATGTTAAAATATCTGTTTGGAGTTAAAACAAAGCGGTACAGTGGAATC
  TTTTCCGTGGTGTATAGTACAGTTGCTGTGTTGCAGAATGTTAAAAACCTCAACGTGTGT
  TCCCTAGGCGTCGGGCTGATGGTTTTTGGTTTGCTGTTGGGTGGCAAGGAGTTTAATGAG
  AGATTTAAAGAGAAATTGCCGGCGCCTATTCCTTTAGAGTTCTTTGCGGTCGTAATGGGA
  ACTGGCATTTCAGCTGGGTTTAACTTGAAAGAATCATACAATGTGGATGTCGTTGGAACA
  CTTCCTCTAGGGCTGCTACCTCCAGCCAATCCGGACACCAGCCTCTTCCACCTTGTGTAC
  GTAGATGCCATTGCCATAGCCATCGTTGGATTTTCAGTGACCATCTCCATGGCCAAGACC
  TTAGCAAATAAACATGGCTACCAGGTTGACGGCAATCAGGAGCTCATTGCCCTGGGACTG
  TGCAATTCCATTGGCTCACTCTTCCAGACCTTTTCAATTTCATGCTCCTTGTCTCGAAGC
  CTTGTTCAGGAGGGAACCGGTGGGAAGACACAGCTTGCAGGTTGTTTGGCCTCATTAATG
  ATTCTGCTGGTCATATTAGCAACTGGATTCCTCTTTGAATCATTGCCCCAGACCATCTGG
  CTTACCACTTTTGTGTCCTCCTTGTTCCTGGGATTGGACTATGGTTTGATCACTGCTGTG
  ATCATTGCTCTGCTGACTGTGATTTACAGAACACAGAGTCCAAGCTACAAAGTCCTTGGA
  AAGCTTCCTGAAACTGATGTGTATATTGATATAGACGCATATGAGGAGGTGAAAGAAATT
  CCTGGAATAAAAATATTTCAAATAAATGCACCAATTTACTATGCAAATAGCGACTTGTAT
  AGCAATGCATTAAAACGAAAGACTGGAGTGAACCCAGCAGTCATCATGGGAGCAAGGAGA
  AAGGCCATGCGGAAGTACGCTAAGGAAGTCGGAAATGCAAATATGGCCAACGCAACTGTT
  GTCAAAGCAGATGCAGAAGTAGATGGAGAGGATGCTACCAAGCCTGAAGAAGAGGATGGT
  GAAGTAAAATATCCCCCAATAGTGATCAAAAGCACATTTCCTGAGGAAATGCAAAGATTT
  ATGCCCCCAGGGGATAACGTCCACACTGTCATTTTGGATTTCACTCAAGTCAATTTTATT
  GATTCTGTTGGAGTGAAAACTCTGGCAGGGATTGTAAAAGAATATGGAGACGTCGGTATA
  TATGTATACTTAGCAGGATGCAGTGCACAAGTTGTGAATGACCTCACTCGGAATAGATTT
  TTTGAAAATCCTGCCCTATGGGAGCTGCTGTTCCACAGCATTCATGATGCAGTTTTAGGC
  AGCCAACTTAGAGAGGCACTTGCTGAACAGGAAGCCTCGGCTCCCCCTTCCCAGGAGGAC
  TTGGAGCCCAATGCCACTCCTGCCACTCCTGAGGCATAG
  
• Restriction Sites: Please inquire
• ACCN: NM_001167962
• ORF Size: 2139 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_001167962.1, NP_001161434.1
• RefSeq Size: 2601
• RefSeq ORF: 2139
• Locus ID: 375611
• Protein Families: Transmembrane
• Gene Summary: This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2009]
  Transcript Variant: This variant (e) lacks an alternate in-frame exon in the 3' coding region, compared to variant a. The resulting isoform (e) lacks an internal segment, compared to isoform a.