AFG3L2 Polyclonal Antibody

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.

Research Area: Cancer, Cell Biology, Metabolism, Neuroscience, Signal Transduction

Synonyms:
AFG3L2, SCA28, SPAX5

Immunogen: Recombinant fusion protein of human AFG3L2 (NP_006787.2).

Swissprot: Q9Y4W6
Gene ID: 10939

Calculated MW: 88 kDa
Observed MW: 89 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "WB 1:200-1:2000 IHC 1:50-1:200"

Storage:
Store at -20°C. Avoid freeze / thaw cycles.