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ATP7A Polyclonal Antibody

CAT: 0866-RD78920A-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0866-RD78920A-01Size:20 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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.
Description
This is a ATP7A Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Synonyms
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++ transporti
Swiss Prot
Q04656
Accession Number
NP_000043
Reactivity
Human, Mouse, Rat
Immunogen
Synthetic peptide of human ATP7A
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
IHC, ELISA
Purification Method
Affinity purification
Assay Type
Antibody
Concentration
0.5 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Host or Source
Rabbit
Isotype
IgG

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