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TUFM Products

TUFM 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. [provided by RefSeq]

3 results for "TUFM" in Products

3 results for "TUFM" in Products

TUFM Products

TUFM 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. [provided by RefSeq]
Applications: IHC, WB, ICC/IF, IP, KD
Reactivity: Human, Rat
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human
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