Thymidine Kinase 2, Mitochondrial (TK2)

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Mt-TK

Thymidine Kinase 2, Mitochondrial (TK2)
TK2 encodes a deoxyribonucleoside kinase that specifically phosphorylates thymidine, deoxycytidine, and deoxyuridine. The encoded enzyme localizes to the mitochondria and is required for mitochondrial DNA synthesis. Mutations in this gene are associated with a myopathic form of mitochondrial DNA depletion syndrome. Alternate splicing results in multiple transcript variants.
The gene encodes a 234-amino acid polypeptide. Although TK2 is believed to reside in mitochondria, it contains no mitochondrial translocation signal sequence. Northern blot analysis revealed that TK2 was ubiquitously expressed as 2 transcripts of 2.4 and 4 kb. Expression of the TK2 cDNA resulted in a 60-kD protein.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Thymidine Kinase 2, Mitochondrial (TK2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Thymidine Kinase 2, Mitochondrial (TK2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Thymidine Kinase 2, Mitochondrial (TK2) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Thymidine Kinase 2, Mitochondrial (TK2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Thymidine Kinase 2, Mitochondrial (TK2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Thymidine Kinase 2, Mitochondrial (TK2) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Thymidine Kinase 2, Mitochondrial (TK2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Thymidine Kinase 2, Mitochondrial (TK2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Thymidine Kinase 2, Mitochondrial (TK2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Thymidine Kinase 2, Mitochondrial (TK2) ELISA Kit Customized Service Offer
  1. "Cloning of the cDNA and chromosome localization of the gene for human thymidine kinase 2."J. Biol. Chem. 272:8454-8458(1997) [PubMed] [Europe PMC] [Abstract]
  2. "Human thymidine kinase 2: molecular cloning and characterisation of the enzyme activity with antiviral and cytostatic nucleoside substrates."FEBS Lett. 443:170-174(1999) [PubMed] [Europe PMC] [Abstract]
  3. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The sequence and analysis of duplication-rich human chromosome 16." Nature 432:988-994(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy."Nat. Genet. 29:342-344(2001) [PubMed] [Europe PMC] [Abstract]
  6. "Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA."Neurology 59:1197-1202(2002) [PubMed] [Europe PMC] [Abstract]
  7. "Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes."Mol. Genet. Metab. 84:75-82(2005) [PubMed] [Europe PMC] [Abstract]
  8. "Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion."Neuromuscul. Disord. 15:412-415(2005) [PubMed] [Europe PMC] [Abstract]
  9. "Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticus."Mitochondrion 20:1-6(2015) [PubMed] [Europe PMC] [Abstract]