| Host: |
Rabbit |
| Applications: |
IHC/IF/ELISA |
| Reactivity: |
Human/Mouse/Rat |
| Note: |
STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS. |
| Short Description: |
Rabbit polyclonal antibody anti-Copper-transporting ATPase 1 (591-640 aa) is suitable for use in Immunohistochemistry, Immunofluorescence and ELISA research applications. |
| Clonality: |
Polyclonal |
| Conjugation: |
Unconjugated |
| Isotype: |
IgG |
| Formulation: |
Liquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide. |
| Purification: |
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| Concentration: |
1 mg/mL |
| Dilution Range: |
IHC 1:100-1:300ELISA 1:40000IF 1:50-200 |
| Storage Instruction: |
Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles. |
| Gene Symbol: |
ATP7A |
| Gene ID: |
538 |
| Uniprot ID: |
ATP7A_HUMAN |
| Immunogen Region: |
591-640 aa |
| Specificity: |
ATP7A Polyclonal Antibody detects endogenous levels of ATP7A protein. |
| Immunogen: |
The antiserum was produced against synthesized peptide derived from the human ATP7A at the amino acid range 591-640 |
| Function | ATP-driven copper (Cu(+)) ion pump that plays an important role in intracellular copper ion homeostasis. Within a catalytic cycle, acquires Cu(+) ion from donor protein on the cytoplasmic side of the membrane and delivers it to acceptor protein on the lumenal side. The transfer of Cu(+) ion across the membrane is coupled to ATP hydrolysis and is associated with a transient phosphorylation that shifts the pump conformation from inward-facing to outward-facing state. Under physiological conditions, at low cytosolic copper concentration, it is localized at the trans-Golgi network (TGN) where it transfers Cu(+) ions to cuproenzymes of the secretory pathway. Upon elevated cytosolic copper concentrations, it relocalizes to the plasma membrane where it is responsible for the export of excess Cu(+) ions. May play a dual role in neuron function and survival by regulating cooper efflux and neuronal transmission at the synapse as well as by supplying Cu(+) ions to enzymes such as PAM, TYR and SOD3. In the melanosomes of pigmented cells, provides copper cofactor to TYR to form an active TYR holoenzyme for melanin biosynthesis. |
| Protein Name | Copper-Transporting Atpase 1Copper Pump 1Menkes Disease-Associated Protein |
| Database Links | Reactome: R-HSA-3299685Reactome: R-HSA-6803544Reactome: R-HSA-936837 |
| Cellular Localisation | Golgi ApparatusTrans-Golgi Network MembraneMulti-Pass Membrane ProteinCell MembraneMelanosome MembraneEarly Endosome MembraneCell ProjectionAxonDendritePostsynaptic DensityCycles Constitutively Between The Tgn And The Plasma MembranePredominantly Found In The Tgn And Relocalized To The Plasma Membrane In Response To Elevated Copper LevelsTargeting Into Melanosomes Is Regulated By Bloc-1 ComplexIn Response To GlutamateTranslocates To Neuron Processes With A Minor Fraction At Extrasynaptic SitesIsoform 3: CytoplasmCytosolIsoform 5: Endoplasmic Reticulum |
| Alternative Antibody Names | Anti-Copper-Transporting Atpase 1 antibodyAnti-Copper Pump 1 antibodyAnti-Menkes Disease-Associated Protein antibodyAnti-ATP7A antibodyAnti-MC1 antibodyAnti-MNK antibody |
Information sourced from Uniprot.org
12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance
