AFG3L2 rabbit pAb
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],
Product Specifications
Background
Product Name Alternative
AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)
UniProt
Q9Y4W6
Swiss Prot
Q9Y4W6
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from human AFG3L2. at AA range: 744-793
Target
AFG3L2
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000, ELISA 1:10000-20000
Buffer
-20°C/1 year
Molecular Weight
88kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
88kD
Fragment
IgG
Subcellular Location
Mitochondrion . Mitochondrion inner membrane ; Multi-pass membrane protein .
Other Product Names
AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)
Gene ID (Human)
10939
Available Sizes
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