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ATP7A antibody
ATP7A
Reactivity: Human, Rat, Mouse
IHC, ELISA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-ATP7A Antibody
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Target
See all ATP7A Antibodies
ATP7A
(ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
Reactivity
All reactivities for ATP7A antibodies
Human, Rat, Mouse
Host
All hosts for ATP7A antibodies
Rabbit
Clonality
All clonalities for ATP7A antibodies
Polyclonal
Conjugate
All conjugates for ATP7A antibodies
This ATP7A antibody is un-conjugated
Application
All applications for ATP7A antibodies
Immunohistochemistry (IHC), ELISA
Purification
Affinity purification
Immunogen
Synthetic peptide of human ATP7A
Isotype
IgG
Top Product
Discover our top product ATP7A Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.5 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Handling Advice
Avoid freeze / thaw cycles.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for ATP7A
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Target
ATP7A
(ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
Alternative Name
ATP7A (ATP7A Products )
Synonyms
ATP7A antibody, cal antibody, wu:fc43e01 antibody, zgc:153422 antibody, zgc:158633 antibody, DDBDRAFT_0218568 antibody, DDBDRAFT_0235190 antibody, DDB_0218568 antibody, DDB_0235190 antibody, atpase antibody, Atp7a antibody, kal antibody, atp7a antibody, DSMAX antibody, MK antibody, MNK antibody, SMAX3 antibody, Blo antibody, DXHXS1608e antibody, I14 antibody, Mo antibody, blotchy antibody, br antibody, brindled antibody, mottled antibody, Mnk antibody, ATPase copper transporting alpha antibody, ATPase, Cu++ transporting, alpha polypeptide antibody, P-type ATPase antibody, ATP synthase subunit a antibody, copper-transporting ATPase 1 antibody, ATP7A antibody, atp7a antibody, LOC100049514 antibody, Atp7a antibody, LOC412379 antibody
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.
NCBI Accession
NP_000043
Pathways
Transition Metal Ion Homeostasis , Ribonucleoside Biosynthetic Process
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