Sku |
AAP33797 |
Old sku |
AAPP04863 |
Price |
$99.00 |
Name |
ATP7A Peptide (AAP33797) |
Purchase info |
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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Ueta,A., Unpublished |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 |
Protocol |
|
Tips |
See our General FAQ page. |
Availability |
In Stock |