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Browse our ATP7A (ATP7A) ELISA Kits

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ATPase, Cu++ Transporting, alpha Polypeptide ELISA Kits (ATP7A)
On www.antibodies-online.com are 6 ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) ELISA Kits from 4 different suppliers available. Additionally we are shipping ATP7A Antibodies (105) and ATP7A Proteins (9) and many more products for this protein. A total of 124 ATP7A products are currently listed.
Synonyms:
atp7a, atpase, Blo, blotchy, br, brindled, cal, DDBDRAFT_0218568, DDBDRAFT_0235190, DDB_0218568, DDB_0235190, DSMAX, DXHXS1608e, I14, kal, MK, Mnk, Mo, mottled, SMAX3, wu:fc43e01, zgc:153422, zgc:158633
list all ELISA KIts Gene Name GeneID UniProt
ATP7A 538 Q04656
ATP7A 11977 Q64430
ATP7A 24941 P70705

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ATP7A (ATP7A) ELISA Kits by Reactivity

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Zebrafish ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) interaction partners

  1. A hierarchic gene expression of copper homeostatic genes was demonstrated between atp7a, sp1 (show SP1 ELISA Kits) and sod1 (show SOD1 ELISA Kits) in zebrafish.

  2. The investigators interrogated a genetic screen for embryos phenocopied by copper deficiency, identifying calamity, a mutant defective in the zebrafish ortholog of the Menkes disease gene (atp7a).

Human ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) interaction partners

  1. Cu chaperone function of Atox1 (show ATOX1 ELISA Kits) mediated through Cu transporter ATP7A is required for VEGF (show VEGFA ELISA Kits)-induced angiogenesis via activation of Cu enzyme lysyl oxidase (show LOX ELISA Kits).

  2. Upon neuronal differentiation, transitions in redox states upregulates expression of ATOX1 (show ATOX1 ELISA Kits) and its partner ATP7A, producing higher flux of copper through the secretory pathway.

  3. CTR1 (show SLC31A1 ELISA Kits), ATP7A, and lysyl oxidase (show LOX ELISA Kits) were upregulated in the lung tissues and pulmonary arteries of mice with hypoxia-induced pulmonary hypertension and pulmonary arterial smooth muscle cells.

  4. A total of 11 different ATP7A mutations were identified in the 11 Korean families tested: 3 frameshift, 2 nonsense, 3 large deletions, 2 splice-site, and 1 missense mutation.

  5. Data suggest that even small amounts of functional ATP7A in subjects with genetic diseases associated with mutant ATP7A result in milder phenotypes; this includes Menkes disease, occipital horn syndrome, and X-linked distal motor neuropathy. [REVIEW]

  6. we demonstrate here that (1) AP complexes 1 and 2 of the CCV traffic machinery physically interact with ATP7A.

  7. Twenty-five novel mutations including duplications, missense, and splice site variants enable us to confirm the pathogenic role of ATP7A mutations in Menkes disease and occipital horn syndrome.

  8. Depletion of CCC complex components leads to lack of copper-dependent movement of the copper transporter ATP7A from endosomes, resulting in intracellular copper accumulation and modest alterations in copper homeostasis in humans with CCDC22 (show CCDC22 ELISA Kits) mutations.

  9. This is the first time the activation of pseudo-exons is demonstrated in the ATP7A gene, and it demonstrates the usefulness of RNA analysis, in terms of revealing disease-causing mutations in noncoding regions.

  10. Normal male karyotypes without c.3914A>G mutation on ATP7A gene was showed. Postnatal genetic analysis and normal development confirmed the prenatal diagnosis.

Mouse (Murine) ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) interaction partners

  1. Cu chaperone function of Atox1 (show ATOX1 ELISA Kits) mediated through Cu transporter ATP7A is required for VEGF (show VEGFA ELISA Kits)-induced angiogenesis via activation of Cu enzyme lysyl oxidase (show LOX ELISA Kits).

  2. CTR1 (show SLC31A1 ELISA Kits), ATP7A, and lysyl oxidase (show LOX ELISA Kits) were upregulated in the lung tissues and pulmonary arteries of mice with hypoxia-induced pulmonary hypertension and pulmonary arterial smooth muscle cells.

  3. study characterized the Mottled-dappled deletion in C3H101H carrier females

  4. Results from experiments in mouse model of Menkes disease harboring ATP5a (show ATP5G1 ELISA Kits) mutation, show increase expression of SOD1 (show SOD1 ELISA Kits) and induction of HO-1 (show HMOX1 ELISA Kits) causing iron metabolism disruption and hemolysis due to copper deficiency.

  5. The MPhi ATP7A selectively regulates LPS (show TLR4 ELISA Kits)-induced inflammatory mediators, in part, via modulation of cellular copper availability, whereas neocuproine generally inhibits the production of inflammatory mediators.

  6. a decrease in ATP7A protein expression contributes to impaired SOD3 (show SOD3 ELISA Kits) activity, resulting in O2(*-) overproduction and endothelial dysfunction in blood vessels of type 1 diabetes mellitus.

  7. ATP7A mutations leading to Menkes disease and occipital horn syndrome in human and animal models [Review]

  8. These studies demonstrate the essential role of the Atp7a gene in mouse embryonic development and establish a powerful model for understanding the tissue-specific roles of ATP7A in copper metabolism and disease.

  9. ATP7A-mediated copper homeostasis is important for the formation of pathogenic proteinase-resistant prion protein (show PRNP ELISA Kits)

  10. In the present study we identified a G to C nucleotide exchange in exon 15 of the Atp7a gene in mosaic mutants, which resulted in an arginine to proline substitution in the highly conserved 6th transmembrane domain of the ATP7A protein.

ATP7A Antigen Profile

Antigen Summary

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 cutis laxa, and occipital horn syndrome.

Alternative names and synonyms associated with ATP7A

  • ATPase, Cu++ transporting, alpha polypeptide (ATP7A) Elisa Kit
  • ATPase, Cu++ transporting, alpha polypeptide (atp7a) Elisa Kit
  • P-type ATPase (atp7a) Elisa Kit
  • ATPase protein (atpase) Elisa Kit
  • ATPase, Cu++ transporting, alpha polypeptide (Atp7a) Elisa Kit
  • ATPase, Cu++ transporting, alpha polypeptide (ATP7) Elisa Kit
  • atp7a Elisa Kit
  • atpase Elisa Kit
  • Blo Elisa Kit
  • blotchy Elisa Kit
  • br Elisa Kit
  • brindled Elisa Kit
  • cal Elisa Kit
  • DDBDRAFT_0218568 Elisa Kit
  • DDBDRAFT_0235190 Elisa Kit
  • DDB_0218568 Elisa Kit
  • DDB_0235190 Elisa Kit
  • DSMAX Elisa Kit
  • DXHXS1608e Elisa Kit
  • I14 Elisa Kit
  • kal Elisa Kit
  • MK Elisa Kit
  • Mnk Elisa Kit
  • Mo Elisa Kit
  • mottled Elisa Kit
  • SMAX3 Elisa Kit
  • wu:fc43e01 Elisa Kit
  • zgc:153422 Elisa Kit
  • zgc:158633 Elisa Kit

Protein level used designations for ATP7A

ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome) , ATPase, Cu++ transporting, alpha polypeptide , Menkes disease ATPase , calamity , copper-transporting ATPase 1 , copper-transporting P-type ATPase , copper-transporting ATPase , ATPase protein , kaleidoscope , Copper-transporting ATPase 1 , copper-transporting ATPase 1-like , Cu++-transporting P-type ATPase , Menkes disease-associated protein , copper pump 1 , Menkes protein , menkes disease-associated protein homolog , copper transporting ATPase

GENE ID SPECIES
100071762 Equus caballus
493745 Felis catus
422333 Gallus gallus
465728 Pan troglodytes
564924 Danio rerio
8624390 Dictyostelium discoideum AX4
100049514 Oryzias latipes
100121456 Nasonia vitripennis
100170482 Xenopus (Silurana) tropicalis
100196483 Salmo salar
100392179 Callithrix jacchus
100458533 Pongo abelii
100470212 Ailuropoda melanoleuca
412379 Apis mellifera
100012703 Monodelphis domestica
100075802 Ornithorhynchus anatinus
100550653 Meleagris gallopavo
100561716 Anolis carolinensis
538 Homo sapiens
406185 Canis lupus familiaris
11977 Mus musculus
24941 Rattus norvegicus
397159 Sus scrofa
541275 Bos taurus
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