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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]
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18 results for "TUFM" in Products

18 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]
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Applications: IHC, WB, ICC/IF, IP, KD
Reactivity: Human, Rat
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: WB, ICC/IF
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: IHC, WB, IP
Reactivity: Human
Applications: WB, ELISA, IP
Reactivity: Human
Applications: WB, ELISA
Reactivity: Human
Applications: WB, ELISA, MA, AP
Catalog #: NBP2-36751PEP
Applications: AC
Applications: WB
Reactivity: Human, Mouse
Applications: WB, ICC/IF
Reactivity: E. coli
Catalog #: H00007284-T01
Applications: WB
Applications: WB
Reactivity: Human
Catalog #: NBP1-84890PEP
Applications: AC
Catalog #: NBP1-84889PEP
Applications: AC
Catalog #: NBP2-36752PEP
Applications: AC
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