TFB1M (NM_016020) Human Untagged Clone

CAT#: SC324517

TFB1M (untagged)-Human transcription factor B1, mitochondrial (TFB1M), nuclear gene encoding mitochondrial protein

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: TFB1M
• Synonyms: CGI-75; CGI75; mtTFB; mtTFB1
• Vector: pCMV6-AC
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_016020.1 GAGCGGCGGTGAAGGTCCTGGGTGAGGTAGGGTTGGATGGTGCTTGCCGCGTATCATGGC
  TGCCTCCGGAAAACTCAGCACTTGCCGTCTCCCTCCGTTGCCCACGATTCGAGAAATCAT
  TAAGTTGTTAAGACTGCAAGCAGCGAAGCAGCTATCACAGAATTTCCTCCTGGACTTGAG
  GCTGACAGATAAGATTGTAAGGAAAGCTGGCAATCTGACAAATGCTTATGTTTACGAAGT
  GGGCCCTGGGCCAGGGGGAATCACAAGATCTATTCTTAATGCCGACGTCGCTGAACTTCT
  GGTGGTTGAAAAGGACACTCGATTTATTCCTGGATTACAGATGCTTTCTGATGCAGCACC
  TGGGAAACTGAGAATTGTTCATGGAGATGTCTTGACATTTAAGGTAGAAAAGGCTTTTTC
  AGAAAGTCTTAAAAGACCCTGGGAAGATGATCCTCCAAATGTACATATTATTGGAAATCT
  GCCTTTTAGTGTTTCAACTCCACTGATTATCAAGTGGCTTGAAAATATTTCCTGTAGAGA
  TGGACCTTTTGTTTATGGCAGAACTCAGATGACTTTGACTTTTCAAAAGGAAGTGGCAGA
  GAGACTTGCAGCCAATACAGGAAGCAAACAGCGTAGTCGCCTCTCTGTTATGGCTCAGTA
  CCTCTGCAATGTTCGACACATCTTTACGATTCCAGGACAAGCTTTTGTCCCCAAACCAGA
  GGTGGACGTGGGCGTGGTGCACTTCACTCCCTTGATACAGCCCAAGATAGAGCAGCCATT
  CAAGCTGGTGGAAAAAGTGGTTCAGAATGTATTTCAGTTCCGAAGGAAATACTGCCATCG
  AGGGCTCAGAATGTTATTCCCTGAAGCGCAGCGCTTGGAAAGCACGGGCAGGCTGTTAGA
  GTTGGCAGACATAGACCCTACTCTTCGGCCCCGCCAGCTCTCCATCTCACACTTTAAGAG
  CCTCTGTGATGTATACAGAAAAATGTGTGATGAAGACCCACAACTCTTTGCATATAATTT
  CAGAGAAGAACTCAAGCGAAGAAAAAGCAAAAATGAAGAAAAAGAAGAGGATGACGCAGA
  GAATTACAGACTCTAGCTGCTGCCTGGGGGCGAGCAGCCTACCAGATGTCGATTTGCACT
  ACGTGGAGCTTCTTATATAGGTACTCTTTTGTCTTTACAGAGTGACGATACAAATGCCAA
  TGACCAGATGTGACTTATTTTCCTTTTACTATACAGCTTGGCAGAGAAAATAAATATCAT
  CAAATAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_016020.1 unedited
  TGCCATTGTATACGACTCCTATAGGGCGGCCGGGAACATCGGCCATTACGGCCGGGGGAG
  CGGCGGTGAAGGTCCTGGGTGAGGTAGGGTTGGATGGTGCTTGCCGCGTATCATGGCTGC
  CTCCGGAAAACTCAGCACTTGCCGTCTCCCTCCGTTGCCCACGATTCGAGAAATCATTAA
  GTTGTTAAGACTGCAAGCAGCGAAGCAGCTATCACAGAATTTCCTCCTGGACTTGAGGCT
  GACAGATAAGATTGTAAGGAAAGCTGGCAATCTGACAAATGCTTATGTTTACGAAGTGGG
  CCCTGGGCCAGGGGGAATCACAAGATCTATTCTTAATGCCGACGTCGCTGAACTTCTGGT
  GGTTGAAAAGGACACTCGATTTATTCCTGGATTACAGATGCTTTCTGATGCAGCACCTGG
  GAAACTGAGAATTGTTCATGGAGATGTCTTGACATTTAAGGTAGAAAAGGCTTTTTCAGA
  AAGTCTTAAAAGACCCTGGGAAGATGATCCTCCAAAATGTACATATTATTGGAAATCTGC
  CTTTTAGTGTTTCAACTCCACTGATTATCAGTGGCTTGAAAATATTTCCTGTATAGATGG
  GACCCTTTTTGTTTTAGGGGCAGAACCTTAGATGACTTTGACTTTTCTAAAGGGAAAGTG
  GACAAAGAAGACTTGCAAG
• Restriction Sites: Please inquire
• ACCN: NM_016020
• ORF Size: 1041 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_016020.1, NP_057104.1
• RefSeq Size: 1290
• RefSeq ORF: 1041
• Locus ID: 51106
• Domains: rADc
• Protein Families: Transcription Factors
• Gene Summary: The protein encoded by this gene is a dimethyltransferase that methylates the conserved stem loop of mitochondrial 12S rRNA. The encoded protein also is part of the basal mitochondrial transcription complex and is necessary for mitochondrial gene expression. The methylation and transcriptional activities of this protein are independent of one another. Variations in this gene may influence the severity of aminoglycoside-induced deafness (AID). [provided by RefSeq, Aug 2010]
  Transcript Variant: This variant (1) encodes the longest 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.