AFG3L2 Rabbit Polyclonal Antibody
Product Specifications
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], cofactor:Binds 1 zinc ion per subunit ., function:Putative ATP-dependent protease., similarity:In the C-terminal section; belongs to the peptidase M41 family., similarity:In the N-terminal section; belongs to the AAA ATPase family., tissue specificity:Ubiquitous.
Product Name Alternative
AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)
Gene Name
AFG3L2
Gene ID
10939
Swiss Prot
Q9Y4W6
Host
Rabbit
Reactivity
Human, Rat, Mouse
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
WB, ELISA
Purification
Affinity purification
Dilution
WB 1:500-1:2000, ELISA 1:10000-1:20000
Form
Liquid
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Modification
Unmodified
Molecular Weight
88kDa
Storage Conditions
Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.
Isotype
IgG
Available Sizes
Curated Selection
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