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AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. 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.
2310036I02Rik; AFG3 ATPase family gene 3-like 2; AFG3 ATPase family member 3-like 2; AFG3 like AAA ATPase 2; AFG3 like matrix AAA peptidase subunit 2; AFG3(ATPase family gene 3)-like 2; AFG3L2; AFG3-like AAA ATPase 2; AFG3-like protein 2; AFG3-like protein 2 (Paraplegin-like protein); ATPase family gene 3, yeast; AW260507; Emv66; FLJ25993; par; paraplegin-like protein; SCA28; si:ch211-12e1.4; similar to AFG3-like protein 2 (Paraplegin-like protein); SPAX5
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