APTX Polyclonal Antibody

Background:
This gene encodes a member of the histidine triad (HIT) superfamily. The encoded protein may play a role in single-stranded DNA repair through its nucleotide-binding activity and its diadenosine polyphosphate hydrolase activity. Mutations in this gene have been associated with ataxia-ocular apraxia. Alternatively spliced transcript variants have been identified for this gene.

Research Area: Epigenetics and Nuclear Signaling

Synonyms:
AOA 1, AOA, AOA1, Aprataxin, Aprataxin homolog, Aptx, APTX, Ataxia 1 early onset with hypoalbuminemia, Ataxia1 early onset with hypoalbuminemia, AXA 1, AXA1, EAOH, EOAHA, FHA HIT, FHA-HIT, FLJ20157, Forkhead associated domain histidine triad like, Forkhead associated domain histidine triad like protein, Forkhead-associated domain histidine triad-like protein, MGC1072

Immunogen: Recombinant protein of human APTX

Swissprot: Q7Z2E3
Gene Accession: BC001628

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.3 mg/mL
Dilution: IHC 1:50-1:200

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

Alternative for product with catalog number:
sc-48841/sc-48842/sc-48840/sc-98894