SLC9A6 (NM_001177651) Human Untagged Clone

CAT#: SC329030

SLC9A6 (untagged)-Human solute carrier family 9 (sodium/hydrogen exchanger) member 6 (SLC9A6) transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SLC9A6
• Synonyms: MRSA; NHE6
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001177651, the custom clone sequence may differ by one or more nucleotides
  ATGGACGAGGAGATCGTGTCCGAGAAGCAAGCCGAGGAGAGCCACCGGCAGGACAGCGCC
  AACCTGCTCATCTTCATCCTGCTGCTCACCCTCACCATTCTCACAATCTGGCTCTTCAAG
  CACCGCCGGGCCCGCTTCCTGCACGAAACCGGCCTGGCTATGATTTATGGTCTTTTGGTG
  GGCCTTGTGCTTCGGTATGGCATTCATGTTCCGAGTGATGTAAATAATGTGACCCTGAGC
  TGTGAAGTGCAGTCAAGTCCAACTACCTTACTGGTAAATGTTAGTGGAAAATTTTATGAG
  TATATGCTGAAAGGAGAGATTAGTTCACATGAACTCAATAATGTTCAAGATAATGAAATG
  CTTAGAAAGGTTACTTTTGATCCAGAAGTATTTTTCAACATATTACTTCCTCCTATCATA
  TTTTATGCAGGTTATAGCCTGAAAAGGAGACATTTTTTTCGAAATCTTGGGTCTATCCTA
  GCATACGCTTTTCTTGGAACAGCAATTTCTTGTTTCGTTATTGGGTCAATAATGTATGGC
  TGTGTAACGCTGATGAAGGTAACGGGACAACTTGCAGGAGATTTTTACTTTACAGATTGC
  CTACTGTTTGGTGCCATTGTATCAGCAACTGATCCAGTGACTGTTCTTGCTATATTCCAC
  GAGCTTCAAGTTGATGTTGAACTCTATGCACTTCTTTTTGGTGAAAGTGTCCTCAATGAT
  GCTGTTGCCATAGTGCTGTCCTCCTCAATAGTGGCATACCAGCCAGCTGGAGACAACAGT
  CACACCTTTGATGTCACAGCGATGTTCAAGTCTATTGGGATCTTCCTTGGAATCTTCAGT
  GGATCTTTTGCAATGGGTGCTGCTACTGGAGTGGTGACAGCTTTAGTGACAAAGTTCACC
  AAATTACGGGAGTTCCAGTTGTTGGAGACAGGCCTGTTCTTCTTGATGTCCTGGAGTACC
  TTCCTCTTGGCTGAAGCATGGGGCTTCACAGGTGTAGTTGCAGTATTGTTTTGTGGCATC
  ACACAAGCACATTATACGTATAATAATTTGTCCACGGAGTCTCAGCATAGAACTAAACAG
  TTGTTTGAGCTTCTCAATTTCTTGGCAGAGAATTTCATCTTCTCCTACATGGGGCTGACA
  CTGTTCACCTTCCAGAACCATGTCTTTAACCCAACATTTGTAGTAGGAGCATTTGTTGCT
  ATTTTCTTGGGAAGAGCTGCCAATATTTACCCCTTGTCCCTCTTACTTAATTTGGGTAGA
  AGAAGTAAGATTGGATCAAATTTTCAACACATGATGATGTTTGCTGGCCTTCGTGGTGCA
  ATGGCATTTGCCTTGGCCATTCGAGATACTGCCACTTATGCACGGCAAATGATGTTCAGC
  ACCACGCTTCTGATTGTGTTTTTTACCGTGTGGGTATTTGGTGGTGGCACCACTGCAATG
  CTGTCATGCTTGCATATCAGGGTTGGTGTTGATTCAGACCAAGAACACTTGGGTGTTCCT
  GAAAATGAAAGGAGAACTACCAAAGCAGAGAGTGCTTGGCTTTTCCGGATGTGGTACAAC
  TTTGATCATAACTATCTGAAGCCTCTGCTGACCCACAGCGGGCCTCCGCTGACAACAACA
  CTCCCTGCCTGCTGTGGACCCATCGCCAGGTGCCTCACCAGCCCCCAGGCTTACGAAAAC
  CAGGAACAGTTGAAAGATGATGATTCTGATCTTATTCTCAATGATGGTGACATCAGTTTG
  ACATATGGAGATTCTACTGTGAACACTGAACCGGCCACATCCAGCGCCCCAAGGAGATTT
  ATGGGAAACAGTTCTGAAGATGCCTTGGATCGGGAGCTTGCATTTGGGGACCATGAACTG
  GTCATTCGAGGAACACGCCTGGTTCTTCCAATGGATGATTCTGAACCCCCGCTAAATTTG
  TTAGATAATACGAGACATGGTCCAGCCTAA
  
• Restriction Sites: Please inquire
• ACCN: NM_001177651
• ORF Size: 1950 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_001177651.1, NP_001171122.1
• RefSeq Size: 4620
• RefSeq ORF: 1950
• Locus ID: 10479
• Protein Families: Druggable Genome, Transmembrane
• Protein Pathways: Cardiac muscle contraction
• Gene Summary: This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]
  Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (c) has a shorter N-terminus, compared to isoform a. 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.