ATP7A Peptide (AAP33797)

Data Sheet
 
Sku AAP33797
Old sku AAPP04863
Price $99.00
Name ATP7A Peptide (AAP33797)
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Size 100 ug
Gene ATP7A
Alias symbols MK, MNK, DSMAX, SMAX3
Gene id 538
Description of 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.
Swissprot id Q04656
Protein accession num NP_000043
Nucleotide accession num NM_000052
Protein size 274 amino acids
Molecular weight 30kDa
Application IHC, WB
Partner proteins ATOX1,CP,PDZD11,ATOX1,GLRX
Quality control The peptide is characterized by mass spectroscopy
Key reference Ueta,A., Unpublished
Description This is a synthetic peptide designed for use in combination with anti-ATP7A antibody (Catalog #: ARP33797_T100) made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Product format Lyophilized powder
Reconstitution and storage Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Lead time Domestic: within 24 hours delivery  International: 3-5 business days
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