AFG3L2 Polyclonal Antibody
Partner: Epigentek Group Inc
| Applications: | WB, IHC, IF |
| Description: | This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. |
| Synonym: | AFG3L2; SCA28; SPAX5; AFG3-like protein 2 |
| Shipping Conditions: | Ship on cold packs |
| Usage: | Research Use Only |
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