SKU: WP16001 Categories: ,

AFG3L2 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP16001-100
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Product details

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],

Specifications

Size50μL/100μL
TargetAFG3L2
ReactivityHuman, Mouse
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)88kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; ELISA 1:10000-20000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human AFG3L2. at AA range: 744-793
SpecificityAFG3L2 Polyclonal Antibody detects endogenous levels of AFG3L2
Gene NameAFG3L2
Protein NameAFG3L2
Other NameAFG3-like protein 2; / Paraplegin-like protein
SpeciesHuman
Gene ID10939
UniprotQ9Y4W6,
Species.1Mouse
Gene ID.169597
Uniprot.1Q8JZQ2
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationMitochondrion . Mitochondrion inner membrane; Multi-pass membrane protein .
Tissue ExpressionUbiquitous. Highly expressed in the cerebellar Purkinje cells.
Signaling_pathwayHuman Diseases >> Neurodegenerative disease >> Spinocerebellar ataxia
Research Areas>>Spinocerebellar ataxia
Functioncofactor: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.,
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