SPG7 rabbit pAb
Ref. EK-ES11406
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014],
Chemical properties
Technical inquiry about: EK-ES11406 SPG7 rabbit pAb
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