ATP7A Polyclonal Antibody

SKU: E-AB-16268

Size: 200μL

Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date: 12 months

Category ID_II: Primary Antibodies

Category ID_III: Polyclonal Antibodies

Abbreviation: ATP7A

Target Synonym: ATP 7A;ATP7A;ATP7A;ATPase copper transporting alpha polypeptide;ATPase Cu++ transporting alpha polypeptide (Menkes syndrome);ATPase Cu++ transporting alpha polypeptide;Copper pump 1;Copper transporting ATPase 1;Copper-transporting ATPase 1;Cu++ transporting P type ATPase;DSMAX;FLJ17790;MC 1;MC1;Menkes disease associated protein;Menkes disease-associated protein;Menkes syndrome;MK;MNK;OHS;OTTHUMP00000062077;SMAX3

Research Areas: Cancer;Metabolism;Neuroscience;Signal transduction

Conjugation: Unconjugated

Host: Rabbit

Species reactivity: Human;Mouse;Rat

Application: IHC

Isotype: IgG

Clonality: Polyclonal

Clone NO.:

UNIProt ID: Q04656

Accession:

Background: This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Concentration: 0.5 mg/mL

Immunogen: Synthetic peptide of human ATP7A

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Dilution: IHC 1:50-1:200

Calculated MW:

ObservedMW: