Anti-TUFM Polyclonal Antibody, 20.0ul
£72.56
Delivery: 2 weeks
SKU
K115569P-20.0ul
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.
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.
- Size: 20.0ul
- Molecular Weight: 50kDa
- Physical State: Liquid
- Storage: Store at -20℃. Avoid freeze / thaw cycles.
- Application: WB;IHC
- Brand: Saint Michael
- Catalogue No.: K115569P-20.0ul
For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.
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