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          • Primary Antibodies ›
          • ATP7A Antibodies

          Antibodies Inc

          Copper ATPase 1 (Menke's Disease Protein) Monoclonal Antibody (L60/4)

          View all (16) ATP7A antibodies

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          Cite Copper ATPase 1 (Menke's Disease Protein) Monoclonal Antibody (L60/4)

          Additional Information:
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          • Antibody Testing Data (1)
          Copper ATPase 1 (Menke's Disease Protein) Antibody in Immunohistochemistry (Frozen) (IHC (F))
          Group 53 Created with Sketch.
          Copper ATPase 1 (Menke's Disease Protein) Antibody in Immunohistochemistry (Frozen) (IHC (F))
          Group 53 Created with Sketch.

          FIGURE: 1 / 1

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          Copper ATPase 1 (Menke's Disease Protein) Antibody (75-142) in IHC (F)

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          Copper ATPase 1 (Menke's Disease Protein) Antibody in Immunohistochemistry (Frozen) (IHC (F))
          Copper ATPase 1 (Menke's Disease Protein) Monoclonal Antibody (L60/4)

          Product Details

          75-142

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          Assay-dependent
          -

          Immunohistochemistry (Frozen) (IHC (F))

          Assay-dependent
          -

          Immunocytochemistry (ICC/IF)

          Assay-dependent
          -

          ELISA (ELISA)

          Assay-dependent
          -

          Immunoprecipitation (IP)

          Assay-dependent
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Mouse / IgG2b

          Class

          Monoclonal

          Type

          Antibody

          Clone

          L60/4

          Immunogen

          Synthetic peptide amino acids 42-61 (cytoplasmic N- terminus) of human Copper-transporting ATPase 1 (accession number Q04656).
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated
          • FL490
          • FL550
          • FL594
          • FL650
          • Request custom conjugation

          Form

          Liquid

          Concentration

          1 mg/mL

          Amount

          100 µg

          Purification

          Protein A

          Storage buffer

          TBS, pH 7.4

          Contains

          0.065% sodium azide

          Storage conditions

          Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

          Shipping conditions

          Ambient (domestic); Dry ice (international)

          Product Specific Information

          For maximum recovery of product, centrifuge the vial prior to removing the cap.

          Target Information

          ATP7A (also known as Copper-transporting ATPase 1) functions as a transmembrane copper-translocating P-type ATPase and plays a vital role in systemic copper absorption in the gut and copper reabsorption in the kidney. Polarized epithelial cells such as Madin-Darby canine kidney cells are a physiologically relevant model for systemic copper absorption and reabsorption in vivo. Although ATP7A is not detectable in most normal tissues, it is expressed in a considerable fraction of many common tumor types. Increased expression of ATP7A renders cells resistant to cisplatin and carboplatin. Mutations in the ATP7A gene result in Menkes disease, which is fatal in early childhood.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: ATP 7A; ATP7A; ATPase, Cu++ transporting, alpha polypeptide; Copper pump 1; Copper-transporting ATPase 1; Cu++-transporting P-type ATPase; FLJ17790; MC 1; Menke; Menkes disease-associated protein; Menkes disease-associated protein homolog; Menkes protein; Menkes syndrome; OHS; OTTHUMP00000062077; unnamed protein product

          View more View less

          Gene Aliases: ATP7A; DSMAX; HMNX; MC1; MK; MNK; SMAX3

          View more View less

          UniProt ID: (Human) Q04656, (Mouse) Q64430, (Rat) P70705

          View more View less

          Entrez Gene ID: (Human) 538, (Mouse) 11977, (Rat) 24941

          View more View less

          Function(s)
          nucleotide binding copper ion transmembrane transporter activity copper ion binding protein binding ATP binding ATPase activity, coupled to transmembrane movement of ions, phosphorylative mechanism superoxide dismutase copper chaperone activity ATPase activity cation-transporting ATPase activity copper-dependent protein binding copper-transporting ATPase activity metal ion binding P-type monovalent copper transporter activity cuprous ion binding copper-exporting ATPase activity hydrolase activity molecular_function primary active transporter
          Process(es)
          blood vessel development release of cytochrome c from mitochondria blood vessel remodeling regulation of oxidative phosphorylation tryptophan metabolic process tyrosine metabolic process catecholamine metabolic process ion transport cation transport copper ion transport cellular copper ion homeostasis mitochondrion organization locomotory behavior glycoprotein biosynthetic process detoxification of copper ion regulation of gene expression copper ion import removal of superoxide radicals cerebellar Purkinje cell differentiation pyramidal neuron development central nervous system neuron development extracellular matrix organization collagen fibril organization hair follicle morphogenesis T-helper cell differentiation epinephrine metabolic process norepinephrine metabolic process dopamine metabolic process norepinephrine biosynthetic process serotonin metabolic process pigmentation negative regulation of neuron apoptotic process skin development negative regulation of catecholamine metabolic process ATP metabolic process positive regulation of melanin biosynthetic process elastic fiber assembly lung alveolus development neuron projection morphogenesis dendrite morphogenesis cartilage development neuron apoptotic process establishment of localization in cell copper ion export neuron cellular homeostasis transport plasma membrane copper ion transport peptidyl-lysine modification metal ion transport hindlimb morphogenesis positive regulation of catalytic activity negative regulation of catalytic activity response to copper ion positive regulation of oxidoreductase activity elastin biosynthetic process in utero embryonic development lactation response to iron(III) ion response to zinc ion
          It has to be done as per old AB suggested Products section.

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