ATP7A Polyclonal Antibody
Product Sizes
20 ul
£118.00
E-AB-16268-20UL
60 ul
£183.00
E-AB-16268-60UL
120 ul
£272.00
E-AB-16268-120UL
200 ul
£420.00
E-AB-16268-200UL
About this Product
- SKU:
- E-AB-16268
- Additional Names:
- ATP 7A,ATP7A,ATPase Cu++ transporting alpha polypeptide,ATPase Cu++ transporting alpha polypeptide (Menkes syndrome),ATPase copper transporting alpha polypeptide,Copper pump 1,Copper transporting ATPase 1,Copper-transporting ATPase 1,Cu++ transporti
- Application:
- Immunohistochemistry
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Clonality:
- Polyclonal
- Concentration:
- 0.5 mg/ml
- Extra Details:
- 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.
- Host:
- Rabbit
- Immunogen:
- Synthetic peptide of human ATP7A
- Isotype:
- IgG
- Purification:
- Affinity Purified
- Reactivities:
- Human, Mouse, Rat
- Shipping Conditions:
- Blue Ice
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Type:
- Antibody: Polyclonal Antibody
- Manufacturer's Data Sheet:p-atp7a_polyclonal_antibody-e_ab_16268
