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Aprataxin Antibody

The Aprataxin gene was identified by linkage analysis as the defective gene in the neurogenerative disorder ataxia with oculomotor apraxia type 1 (AOA1) which is characterized by cerebellar ataxia, peripheral neuropathy, and hypoalbuminemia. Aprataxin functions in the DNA damage response and is involved in single-strand and double-strand break repair, and base excision repair.
APTX
aprataxin
Aprataxin
:  AOA AOA1 ataxia 1, early onset with hypoalbuminemia AXA1 EAOH EOAHA FHA-HIT FLJ20157 forkhead-associated domain histidine triad-like protein
Product
Specifications
Ordering Information
Human
WB, IP
Between 100 and 150
100
$339
$229
$99