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ATPase, Cu++ Transporting, beta Polypeptide Proteins (ATP7B)

ATP7B is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. Additionally we are shipping ATP7B Antibodies (129) and ATP7B Kits (7) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
ATP7B 540 P35670
ATP7B 11979 Q64446
Rat ATP7B ATP7B 24218  
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Top ATP7B Proteins at antibodies-online.com

Showing 6 out of 10 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 69 to 74 Days
$9,050.32
Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 69 to 74 Days
$12,906.52
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

ATP7B Proteins by Origin and Source

Origin Expressed in Conjugate
Human , , ,
, ,
Mouse (Murine) ,
,

More Proteins for ATPase, Cu++ Transporting, beta Polypeptide (ATP7B) Interaction Partners

Cow (Bovine) ATPase, Cu++ Transporting, beta Polypeptide (ATP7B) interaction partners

  1. Data show that CD4 (show CD4 Proteins)(+) and WC1(+) gammadelta T-cells were induced to produce IL-17 (show IL17A Proteins) termed Th17 and gammadelta17 cells.

  2. The endocytosis and signaling of the gamma-delta T cell coreceptor WC1 are regulated by a dileucine motif.

  3. WC1 is a hybrid gamma-delta TCR coreceptor and pattern recognition receptor for pathogenic bacteria.

  4. Identification of differences in the signal transduction through the endodomains of WC1 contributes to understanding the functional role of the WC1 coreceptors in the gammadelta T cell responses.

  5. Specific receptors in the WC1 family directly participate in Leptospira recognition and/or activation of gamma-delta T cells.

  6. These findings revealed that despite the existence of a distinct bovine CD4 (show CD4 Proteins)(+)CD25 (show IL2RA Proteins)(high) T cell population, which showed Foxp3 (show FOXP3 Proteins) transcription/expression, natural regulatory activity did not reside in this cell population

  7. Sudies demonstrate that WC1 molecules are encoded by a large, multi-gene family whose transcripts undergo extensive alternative splicing.

Human ATPase, Cu++ Transporting, beta Polypeptide (ATP7B) interaction partners

  1. With the capability of generating relatively higher throughput in a short time period, the NGS assay is a viable alternative to Sanger sequencing for detecting ATP7B mutations causally linked to Wilson disease in the clinical diagnostic laboratory

  2. analysis of the geographic distribution of ATP7B mutations in Wilson disease [review]

  3. Extrinsic expressing WT ATP7B reduced CuCl2-induced copper accumulation and enhanced cellular copper tolerance by accelerating copper excretion, which was selectively compromised by R778L and P992L mutations.

  4. Metal-dependent movement of the first four metal-binding domains in ATP7B may be a trigger that initiates the overall catalytic cycle.

  5. Nine out of the thirty-two pediatric Turkish WD patients had no mutations in the ATP7B gene.

  6. Novel mutation of the ATP7B gene was found in Chinese families with pre-symptomatic Wilson's disease.

  7. Wilson disease causing p.T788I, p.V1036I and p.R1038G-fsX83 mutations lead to functional deficiency in ATP7B protein.

  8. The present results demonstrate the design and evaluation of a low-density microarray for the detection of 62 mutations in ATP7B gene, and show that a microarray based approach can be cost-effective for detecting a large number of mutations simultaneously

  9. Screening for the two exons 14 and 18 of the ATP7B gene is important in Egyptian patients especially in suspected patients without hepatic manifestations.

  10. The ATP7B gene testing for the boy, his sister, and their parents detected two novel missense mutations in the boy and his sister, i.e., compound heterozygous mutations in exon 7 and exon 13

Mouse (Murine) ATPase, Cu++ Transporting, beta Polypeptide (ATP7B) interaction partners

  1. Data indicate that the copper-transporting ATPase gene (Atp7b) knockout mice showed a drastic, time-dependent accumulation of hepatic copper.

  2. The aim of this study was to identify copper disturbances according to various brain compartments and further dissect the causal relationship between copper storage and neuronal damage using Atp7b(-/-) mice.

  3. DKWSLLL sequence is essential for ATP7b sorting at the TGN (show TG Proteins), transport from the TGN (show TG Proteins) to the PM, endocytosis, and recycling to the TGN (show TG Proteins) and PM.

  4. Ligand-activated nuclear receptors FXR/NR1H4 (show NR1H4 Proteins) and GR/NR3C1 (show NR3C1 Proteins) and nuclear receptor interacting partners are less abundant in Atp7b(-/-) hepatocyte nuclei.

  5. By performing dynamic PET, authors obtained the first real-time measurements of 64Cu distribution in the organs or tissues of Atp7b -/- mice.

  6. Clusterin (show CLU Proteins) and COMMD1 (show COMMD1 Proteins) independently regulate degradation of the mammalian copper ATPases ATP7A (show ATP7A Proteins) and ATP7B.

  7. Neuroinflammatory and behavioural changes in the Atp7B mutant mouse model of Wilson's disease.

  8. The Jackson toxic milk mouse as a model for copper loading

  9. Both Atp7a (show ATP7A Proteins) and Atp7b are expressed in glomeruli; however, Atp7b is also seen in the kidney medulla suggesting that glomeruli are responsible for regulating copper levels in the filtrate

  10. Mice homozygous for the recessive txJ mutation examined at 6 months of age exhibited a reduced number of amyloid plaques and diminished plasma Abeta (show APP Proteins) levels. Homozygosity for txJ increased survival and lowered endogenous CNS Abeta (show APP Proteins).

Pig (Porcine) ATPase, Cu++ Transporting, beta Polypeptide (ATP7B) interaction partners

  1. A copper-dependent ATPase hydrolysis in a native Golgi-enriched preparation from liver, was characterized.

ATP7B Protein Profile

Protein Summary

This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).

Gene names and symbols associated with ATP7B

  • ATPase, Cu++ transporting, beta polypeptide (ATP7B)
  • ATPase, Cu++ transporting, beta polypeptide (atp7b)
  • ATPase, Cu++ transporting, beta polypeptide (Wilson disease) (atp7b)
  • ATPase, Cu++ transporting, beta polypeptide (LOC100344865)
  • ATPase, Cu++ transporting, beta polypeptide (Atp7b)
  • BoWC1.1 (WC1)
  • CD163 molecule-like 1 (CD163L1)
  • Atp7a protein
  • ATP7B protein
  • Hts protein
  • PINA protein
  • PWD protein
  • tx protein
  • WC1 protein
  • Wd protein
  • WND protein

Protein level used designations for ATP7B

ATPase, Cu++ transporting, beta polypeptide , copper-transporting ATPase beta subunit , ATPase, Cu++ transporting, beta polypeptide (Wilson disease) , Wilson's disease protein , copper-transporting ATPase , copper-transporting ATPase 2 , ATP7B-like , copper-transporting ATPase 2-like , ATPase, Cu(2+)- transporting, beta polypeptide , Wilson disease-associated protein , copper pump 2 , Wilson protein , toxic milk , wilson disease-associated protein homolog , ATPase, Cu++ transporting, beta polypeptide (same as Wilson disease) , PINA gene, promoter , pineal night-specific ATPase , ATPase, Cu(2+)-transporting, beta polypeptide , ATPase 7B protein , scavenger receptor cysteine-rich type 1 protein M160 , scavenger-receptor protein

GENE ID SPECIES
518075 Bos taurus
442967 Canis lupus familiaris
476903 Canis lupus familiaris
556499 Danio rerio
571325 Danio rerio
592143 Strongylocentrotus purpuratus
713781 Macaca mulatta
100344865 Oryctolagus cuniculus
100469748 Ailuropoda melanoleuca
100497797 Xenopus (Silurana) tropicalis
100028163 Monodelphis domestica
100082671 Ornithorhynchus anatinus
100052751 Equus caballus
100541545 Meleagris gallopavo
100558446 Anolis carolinensis
540 Homo sapiens
11979 Mus musculus
24218 Rattus norvegicus
418879 Gallus gallus
100049684 Sus scrofa
443046 Ovis aries
783109 Bos taurus
100144477 Sus scrofa
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