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
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late March 2018 (Updated 02/15/2018)
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late March 2018 (Updated 02/15/2018)
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late March 2018 (Updated 02/15/2018)