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ATP7A Antibody Blocking Peptide Summary
Description
A human ATP7A antibody blocking peptide.
Source: Synthetic
(Accession #: NP_000043)
Source
Synthetic
Protein/Peptide Type
Antibody Blocking Peptide
Gene
ATP7A
Purity
N/A
Applications/Dilutions
Dilutions
Antibody Competition
Application Notes
This peptide is useful as a blocking peptide for NBP1-54906. This synthetic peptide is designed for use in an antibody competition assay with its corresponding antibody. Use of this product in any other assay has not yet been tested.For further blocking peptide related protocol, click here.
Publications
Read Publication using NBP1-54906PEP in the following applications:
Reconstitute with 100ul of sterile PBS for a final peptide concentration of 1 mg/ml.
Notes
For longer periods of storage, aliquot and store at -20C. Avoid repeat freeze-thaw cycles.
Alternate Names for ATP7A Antibody Blocking Peptide
ATPase, Cu++ transporting, alpha polypeptide
Copper pump 1
copper-transporting ATPase 1
Cu++-transporting P-type ATPase
DSMAX
EC 3.6.3
EC 3.6.3.4
MC1
Menkes disease-associated protein
Menkes syndrome
MK
MNKFLJ17790
OHS
SMAX3
Background
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.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.
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