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ATPase, H+ Transporting, Lysosomal 56/58kDa, V1 Subunit B1 (ATP6V1B1) ELISA Kits

ATP6V1B1 encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. Additionally we are shipping ATP6V1B1 Antibodies (80) and ATP6V1B1 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human ATP6V1B1 ATP6V1B1 525 P15313
Anti-Mouse ATP6V1B1 ATP6V1B1 110935  
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More ELISA Kits for ATP6V1B1 Interaction Partners

Human ATPase, H+ Transporting, Lysosomal 56/58kDa, V1 Subunit B1 (ATP6V1B1) interaction partners

  1. ATP6V1B1 genetic mutations were detected in more than half of the families studied. Mutations in this gene therefore seem to be the most common causative factors in hearing loss associated with distal renal tubular acidosis in these families.

  2. Two founder mutations in the ATP6V1B1 gene were found in 16/27 dRTA cases.

  3. Two probands from different kindreds with mutations in ATP6V1B1 presented early onset profound sensorineural hearing loss

  4. Rare and family-specific variants in ATP6V1B1 are responsible for distal renal tubular acidosis and sensorineural hearing loss syndrome in Turkey.

  5. Mutations of the ATP6V1B1 gene is associated with primary distal renal tubular acidosis.

  6. Three ATP6V1B1 mutations were observed: one frameshift mutation in exon 12; a G to C single nucleotide substitution, on the acceptor splicing site in intron 2, and one novel missense mutation in exon 11.

  7. Data indicate that direct sequencing of the ATP6V1B1 gene showed one patient harbors two homozygous mutations and the other one is a compound heterozygous.

  8. Only two ATP6V1B1 mutations are found in a Cypriot population with distal renal tubular acidosis.

  9. This study indicated that a significant percentage of the children with DRTA had sensorineural hearing loss and mutation in ATP6V1B1 gene.

  10. Two siblings with distal renal tubular acidosis and sensorineural deafness having mutation in the first coding exon of the ATP6V1B1 gene , resulting in a non functional protein, are reported. The parents were found to be carriers for the mutation.

Cow (Bovine) ATPase, H+ Transporting, Lysosomal 56/58kDa, V1 Subunit B1 (ATP6V1B1) interaction partners

  1. vH(+)-ATPase (show DNAH8 ELISA Kits) has been detected in the cell membrane and in intracellular pools in bovine rumen epithelium.

Mouse (Murine) ATPase, H+ Transporting, Lysosomal 56/58kDa, V1 Subunit B1 (ATP6V1B1) interaction partners

  1. Aldosterone increases V-ATPase-dependent proton secretion in clear cells in the caput epididymis via MR/NR3C2 and PKC activation.

  2. Data conclude that V-ATPase (show ATP6V1H ELISA Kits)-mediated H(+) secretion in the olfactory epithelium is required for optimal olfactory function.

  3. Provide comprehensive protein expression profiles of specialized V-ATPase-B1-expressing cells in the kidney and epididymis.

  4. Redistribution of Atp6v1b2 (show ATP6V1B2 ELISA Kits) occurs from intracellular compartments into the apical membrane of epididymal clear cells from Atp6v1b1(-/-) mice.

  5. In mice that lack a functional B1 subunit of the V-ATPase (show ATP6V1H ELISA Kits), sAC (show ADCY10 ELISA Kits) was colocalized apically in A-IC along with V-ATPase (show ATP6V1H ELISA Kits) containing the alternative B2 subunit isoform.

  6. Gene ablation abolished the enhanced urinary acidification stimulated by exposure of dissected outer medullary collecting ducts to high (5.0 mM) extracellular Ca(2 (show CA2 ELISA Kits)+).

ATP6V1B1 Antigen Profile

Antigen Summary

This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle 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. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness.

Gene names and symbols associated with ATP6V1B1

  • ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1 (ATP6V1B1) antibody
  • ATPase, H+ transporting, lysosomal V1 subunit B1 (Atp6v1b1) antibody
  • Atp6b1 antibody
  • AW208839 antibody
  • D630003L15 antibody
  • D630030L16Rik antibody
  • D630039P21Rik antibody
  • RTA1B antibody
  • VATB antibody
  • VMA2 antibody
  • Vpp-3 antibody
  • Vpp3 antibody

Protein level used designations for ATP6V1B1

H(+)-transporting two-sector ATPase, 58kD subunit , H+-ATPase beta 1 subunit , V-ATPase B1 subunit , V-ATPase subunit B 1 , V-type proton ATPase subunit B, kidney isoform , endomembrane proton pump 58 kDa subunit , vacuolar proton pump 3 , vacuolar proton pump subunit B 1 , vacuolar proton pump, subunit 3 , ATPase, H+ transporting, V1 subunit B1 , ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1 (Renal tubular acidosis with deafness) , vacuolar H+-ATPase , ATPase, H+ transporting, V1 subunit B , ATPase, H+ transporting, lysosomal (vacuolar proton pump), beta 56/58 kDa , ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B , lysosomal 56/58kDa

GENE ID SPECIES
525 Homo sapiens
338059 Bos taurus
110935 Mus musculus
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