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AFG3L2


Official Full Name
AFG3 like matrix AAA peptidase subunit 2
Organism
Homo sapiens
Gene ID
10939
Background
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. [provided by RefSeq, Jul 2008]
Synonyms
OPA12; SCA28; SPAX5

Cat.No. Product Name Price
SHH233034 shRNA set against Human AFG3L2 (NM_006796.2) Inquiry
SHH233038 shRNA set against Mouse AFG3L2 (NM_027130.1) Inquiry
SHH233042 shRNA set against Rat AFG3L2 (NM_001134864.1) Inquiry
SHW012135 shRNA set against Danio rerio AFG3L2 (NM_001111197) Inquiry
Cat.No. Product Name Price
CDFR010039 Rat Afg3l2 cDNA Clone(NM_001134864.1) Inquiry
MiUTR1M-01286 AFG3L2 miRNA 3'UTR clone Inquiry
MiUTR3H-06928 AFG3L2 miRNA 3'UTR clone Inquiry
CDCB173610 Danio rerio AFG3L2 ORF Clone (NM_001111197) Inquiry
CDCB187883 Rabbit AFG3L2 ORF clone (XM_008261014.1) Inquiry
CDCR025398 Human AFG3L2 ORF clone (NM_006796.2) Inquiry
CDCR259809 Mouse Afg3l2 ORF Clone(NM_027130.1) Inquiry
CDCR377050 Rat Afg3l2 ORF Clone(NM_001134864.1) Inquiry
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