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anti-Human ATP6V1B1 Antikörper:
anti-Mouse (Murine) ATP6V1B1 Antikörper:
anti-Rat (Rattus) ATP6V1B1 Antikörper:
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The aim of this work was to analyze the prevalence of genetic defects in SLC4A1 (zeige SLC4A1 Antikörper), ATP6V0A4 (zeige ATP6V0A4 Antikörper), and ATP6V1B1 genes and to assess the clinical phenotype of distal renal tubular acidosis patients that are eventually typical of the different genetic forms of the disease.
Our data indicate that recurrent stone formers with the vacuolar H(+)-ATPase (zeige ATP6V1B2 Antikörper) B1 subunit p.E161K SNP exhibit a urinary acidification deficit with an increased prevalence of calcium phosphate-containing kidney stones
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.
Two founder mutations in the ATP6V1B1 gene were found in 16/27 dRTA cases.
Two probands from different kindreds with mutations in ATP6V1B1 presented early onset profound sensorineural hearing loss
Rare and family-specific variants in ATP6V1B1 are responsible for distal renal tubular acidosis and sensorineural hearing loss syndrome in Turkey.
Mutations of the ATP6V1B1 gene is associated with primary distal renal tubular acidosis.
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.
Data indicate that direct sequencing of the ATP6V1B1 gene showed one patient harbors two homozygous mutations and the other one is a compound heterozygous.
Only two ATP6V1B1 mutations are found in a Cypriot population with distal renal tubular acidosis.
vH(+)-ATPase (zeige DNAH8 Antikörper) has been detected in the cell membrane and in intracellular pools in bovine rumen epithelium.
Because MRL-Atp6v1b1vxt/vtx mice do not recapitulate the metabolic acidosis of dRTA patients, they provide a new genetic model for nonsyndromic deafness with enlarged vestibular aqueduct (EVA (zeige MPZL2 Antikörper); OMIM #600791).
Dot1l (zeige DOT1L Antikörper) is a new epigenetic regulator of principal cells and intercalated cell differentiation and Atp6v1b1 is a new transcriptional target of Dot1l (zeige DOT1L Antikörper).
Aldosterone increases V-ATPase-dependent proton secretion in clear cells in the caput epididymis via MR/NR3C2 and PKC activation.
Data conclude that V-ATPase (zeige ATP6V1H Antikörper)-mediated H(+) secretion in the olfactory epithelium is required for optimal olfactory function.
Provide comprehensive protein expression profiles of specialized V-ATPase-B1-expressing cells in the kidney and epididymis.
Redistribution of Atp6v1b2 (zeige ATP6V1B2 Antikörper) occurs from intracellular compartments into the apical membrane of epididymal clear cells from Atp6v1b1(-/-) mice.
In mice that lack a functional B1 subunit of the V-ATPase (zeige ATP6V1H Antikörper), sAC (zeige ADCY10 Antikörper) was colocalized apically in A-IC along with V-ATPase (zeige ATP6V1H Antikörper) containing the alternative B2 subunit isoform.
Gene ablation abolished the enhanced urinary acidification stimulated by exposure of dissected outer medullary collecting ducts to high (5.0 mM) extracellular Ca(2 (zeige CA2 Antikörper)+).
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.
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