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ATP7A (ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)) Blocking Peptide (the middle region of protein) (100ug)

ATP7A (ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)) Blocking Peptide (the middle region of protein) (100ug)

Supplier: Aviva Systems Biology Incorporated
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This is a synthetic peptide designed for use in combination with anti-ATP7A antibody (Catalogue #: ARP33798_P050) 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.
Presku: AAP33798
Size: 100 ug
Weight: 163kDa
Gene: 538
Format: Lyophilized powder
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 Gol
Alternative names: MK; MNK
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