Supplier:
Aviva Systems Biology IncorporatedATP7A antibody - N-terminal region (ARP33797_T100)
Prices direct from Aviva Systems Biology Incorporated
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SPECIFICATIONS
Size
100ug
Applications
WB
Hosts
Rabbit
Reactivities
Hum, Can
Format
Lyophilized powder
Presku
ARP33797_T100
Target
The ATP7A gene encodes the Menkes copper-translocating P-type ATPase, a ubiquitous protein that regulates the absorption of copper in the gastrointestinal tract. Inside cells, this protein has a dual function: it delivers copper to cuproenzymes in the Golgi compartment and effluxes excess copper. The trafficking mechanism and catalytic activity combine to facilitate absorption and intercellular transport of copper. Menkes disease, a systemic copper deficiency disorder, is caused by mutations in the ATP7A gene.
Weight
30kDa
Gene Id
538
Alternative Names
MK; MNK; DSMAX; SMAX3
SUPPLIER INFO
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