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Description
This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein 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. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq
Specifications
Specifications
| Antigen | SPG7 |
| Applications | Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Rabbit polyclonal antibody raised against a full-length human SPG7 protein. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | SPG7 |
| Gene Accession No. | NM_003119.2 |
| Gene Alias | CAR/CMAR/FLJ37308/MGC126331/MGC126332/PGN/SPG5C |
| Gene Symbols | SPG7 |
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