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Browse our anti-ATP6V0A4 (ATP6V0A4) Antibodies

Full name:
anti-ATPase, H+ Transporting, Lysosomal V0 Subunit A4 Antibodies (ATP6V0A4)
On www.antibodies-online.com are 34 ATPase, H+ Transporting, Lysosomal V0 Subunit A4 (ATP6V0A4) Antibodies from 10 different suppliers available. Additionally we are shipping ATP6V0A4 Proteins (3) and many more products for this protein. A total of 37 ATP6V0A4 products are currently listed.
Synonyms:
a4, Atp6n1b, ATP6N2, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2
list all antibodies Gene Name GeneID UniProt
ATP6V0A4 50617 Q9HBG4
ATP6V0A4 140494 Q920R6

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Most Popular Reactivities for anti-ATP6V0A4 (ATP6V0A4) Antibodies

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anti-Human ATP6V0A4 Antibodies:

anti-Mouse (Murine) ATP6V0A4 Antibodies:

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Top referenced anti-ATP6V0A4 Antibodies

  1. Human Polyclonal ATP6V0A4 Primary Antibody for IHC - ABIN965622 : Smith, Skaug, Choate, Nayir, Bakkaloglu, Ozen, Hulton, Sanjad, Al-Sabban, Lifton, Scherer, Karet: Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. in Nature genetics 2000 (PubMed)
    Show all 5 references for ABIN965622

More Antibodies against ATP6V0A4 Interaction Partners

Human ATPase, H+ Transporting, Lysosomal V0 Subunit A4 (ATP6V0A4) interaction partners

  1. ITM2A (show ITM2A Antibodies) expression is positively regulated by PKA-CREB (show CREB1 Antibodies) signaling and ITM2A (show ITM2A Antibodies) expression interferes with autophagic flux by interacting with vacuolar ATPase (show DNAH8 Antibodies).

  2. e have described patients with severe distal renal tubular acidosis and a novel splicing mutation in the ATP6V0A4 gene in a family originating from the Siliana region in northwestern Tunisia

  3. Functional analysis of selected regulated proteins revealed that knockdown of HNRPD (show HNRNPD Antibodies), PHB2 (show PHB2 Antibodies) and UB2V2 (show UBE2V2 Antibodies) can increase HCMV replication, while knockdown of A4 and KSRP (show KHSRP Antibodies) resulted in decreased HCMV replication.

  4. For the remaining patients, two mutations in the ATP6V0A4 gene, one of them being novel, were found in three Tunisian cases.

  5. Two from different families carrying ATP6V0A4 mutations manifested early onset moderate mixed HL and moderate SNHL

  6. Mutations of the ATP6V0A4 gene is associated with primary distal renal tubular acidosis.

  7. Case Report: novel ATP6V0A4 gene mutation confirmed autosomal recessive distal renal tubular acidosis with normal hearing.

  8. The function of vacuolar ATPase (V-ATPase (show DNAH8 Antibodies)) a (show ATP6V1A Antibodies) subunit isoforms in invasiveness of MCF10a and MCF10CA1a human breast cancer cells.

  9. Four mutations in the ATP6V0A4 gene were obesrved one single nucleotide deletion in exon 13, the nonsensein exon 3, and the missense changes in exon 17 and in exon 19.

  10. Novel compound heterozygous ATP6V0A4 mutations in an infant with distal renal tubular acidosis.

Mouse (Murine) ATPase, H+ Transporting, Lysosomal V0 Subunit A4 (ATP6V0A4) interaction partners

  1. The first detailed analysis of the structure and function of the auditory system in Atp6v0a4(-/-) knockout mice, is reported.

  2. V-ATPase (show ATP6V1H Antibodies) a4 knockout mice suffer not only from severe acidosis but also from proximal tubule dysfunction with defective endocytic trafficking, proteinuria, phosphaturia and accumulation of lysosomal material.

  3. Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype

  4. Data suggestthat Foxi1 (show FOXI1 Antibodies) is necessary for expression of at least four subunits in three different epithelia and most likely is a major determinant for proper assembly of a functional vacuolar H(+)-ATPase (show ATP6V1B2 Antibodies) complex at these locations.

ATP6V0A4 Antigen Profile

Antigen Summary

This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. This gene is one of four genes in man and mouse that encode different isoforms of the a subunit. Alternatively spliced transcript variants encoding the same protein have been described. Mutations in this gene are associated with renal tubular acidosis associated with preserved hearing.

Alternative names and synonyms associated with ATP6V0A4

  • ATPase, H+ transporting, lysosomal V0 subunit a4 (ATP6V0A4) antibody
  • ATPase, H+ transporting, lysosomal V0 subunit A4 (Atp6v0a4) antibody
  • a4 antibody
  • Atp6n1b antibody
  • ATP6N2 antibody
  • RDRTA2 antibody
  • RTA1C antibody
  • RTADR antibody
  • STV1 antibody
  • VPH1 antibody
  • VPP2 antibody

Protein level used designations for ATP6V0A4

ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1B , ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 2 (38kD) , H(+)-transporting two-sector ATPase, noncatalytic accessory protein 1B , V-ATPase 116 kDa , V-type proton ATPase 116 kDa subunit a , V-type proton ATPase 116 kDa subunit a isoform 4 , vacuolar proton pump 116 kDa accessory subunit , vacuolar proton pump, subunit 2 , vacuolar proton translocating ATPase 116 kDa subunit a kidney isoform , ATPase, H+ transporting, lysosomal (vacuolar proton pump) noncatalytic accessory protein 1B , V-ATPase alpha 4 , vacuolar proton translocating ATPase 100 kDa a4 subunit

GENE ID SPECIES
50617 Homo sapiens
140494 Mus musculus
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