SLC25A46 (NM_001303249) Human Untagged Clone

CAT#: SC335444

SLC25A46 (untagged) - Human solute carrier family 25, member 46 (SLC25A46), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SLC25A46
• Synonyms: HMSN6B
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001303249, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCATCCGCGGCGCCCGGACGGATTTGATGGCTTGGGCTACCGGGGTGGTGCCCGGGACGAGCAGGGCT
  TTGGCGGCGCCTTCCCTGCAAGGTCCTTCAGCACCGGGTCGGACCTGGGCCACTGGGTGACGACTCCCCC
  AGATATCCCCGGCAGCCGCAACCTGCACTGGGGCGAGAAGAGCCCGCCCTACGGCGTGCCCACCACCTCC
  ACCCCGTACGAAGGCCCCACGGAGGAACCCTTTTCCAGTGGCGGCGGCGGCAGTGTGCAGGGGCAGAGCA
  GTGAACAGCTGAATAGATTTGCTGGATTTGGTATTGGACTTGCAAGTCTCTTTACAGAAAATGTATTGGC
  ACATCCTTGCATTGTTCTACGCCGCCAATGTCAGGTTAATTACCATGCTCAGCATTACCATCTCACTCCA
  TTTACAGTCATCAATATTATGTACAGTTTCAACAAAACTCAGGGACCTAGAGCCCTGTGGAAAGGAATGG
  GAAGTACATTTATTGTCCAGGGAGTCACACTTGGAGCAGAAGGCATAATTAGTGAATTTACACCTTTGCC
  AAGGGAGGTTTTACATAAATGGAGTCCTAAACAAATAGGAGAACACCTTCTACTGAAATCCCTAACTTAC
  GTGGTGGCAATGCCTTTTTATTCAGCAAGTCTGATTGAAACAGTGCAGAGTATGTTGGATGCTTATTTTC
  CAGAACTTATTGCTAACTTTGCTGCCAGTCTTTGTTCTGACGTTATACTTTACCCATTGGAAACAGTTTT
  GCACCGCCTTCACATTCAAGGAACACGCACAATAATTGACAATACAGACCTTGGCTATGAAGTGCTTCCA
  ATTAATACACAATATGAGGGAATGAGAGACTGTATCAATACCATAAGGCAGGAGGAAGGAGTGTTTGGTT
  TTTATAAAGGGTTTGGTGCTGTTATAATACAGTACACACTGCATGCAGCTGTTTTACAGATTACCAAAAT
  TATTTACTCTACACTTCTTCAAAATAACATTTGA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001303249
• ORF Size: 1014 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).

Reference Data

• RefSeq: NM_001303249.1, NP_001290178.1
• RefSeq Size: 4519
• RefSeq ORF: 1014
• Locus ID: 91137
• Gene Summary: This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]
  Transcript Variant: This variant (2) uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. The encoded isoform (2) is shorter than 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.