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Invitrogen™ TUFM Recombinant Rabbit Monoclonal Antibody (HL2117)

Description
TUFM Recombinant Monoclonal Antibody for Western Blot, IHC (P)
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
Specifications
Specifications
| Antigen | TUFM |
| Applications | Immunohistochemistry (Paraffin), Western Blot |
| Classification | Recombinant Monoclonal |
| Clone | HL2117 |
| Concentration | 1 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with no preservative |
| Gene | TUFM |
| Gene Accession No. | P49411, P85834, Q8BFR5 |
| Gene Alias | 2300002G02Rik; C76308; C76389; COXPD4; D250; EFTU; EF-Tu; EF-TuMT; elongation factor Tu; elongation factor Tu, mitochondrial; fi06f04; P43; Tu translation elongation factor, mitochondrial; TUFM; tufm {ECO:0000250; UniProtKB:P49411}; wu:fi06f04; zgc:110766 |
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