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anti-Rat (Rattus) SLC26A6 Antibodies:
anti-Human SLC26A6 Antibodies:
anti-Mouse (Murine) SLC26A6 Antibodies:
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Human Polyclonal SLC26A6 Primary Antibody for IHC, IHC (p) - ABIN4354206
Ilves, Virolainen, Harvima: Immediate Wheal Reactivity to Autologous Sweat in Atopic Dermatitis Is Associated with Clinical Severity, Serum Total and Specific IgE and Sweat Tryptase Activity. in International archives of allergy and immunology 2016
Human Polyclonal SLC26A6 Primary Antibody for ELISA, WB - ABIN566296
Abdulnour-Nakhoul, Nakhoul, Kalliny, Gyftopoulos, Rabon, Doetjes, Brown, Nakhoul: Ion transport mechanisms linked to bicarbonate secretion in the esophageal submucosal glands. in American journal of physiology. Regulatory, integrative and comparative physiology 2011
Human Polyclonal SLC26A6 Primary Antibody for WB - ABIN528767
Musch, Arvans, Wu, Chang: Functional coupling of the downregulated in adenoma Cl-/base exchanger DRA and the apical Na+/H+ exchangers NHE2 and NHE3. in American journal of physiology. Gastrointestinal and liver physiology 2009
IL-4 (show IL4 Antibodies) induces demethylation of specific CpG sites within the pendrin (show SLC26A4 Antibodies) promoter. These epigenetic alterations are cell type specific, and may in part dictate pendrin (show SLC26A4 Antibodies) mRNA transcription
Helicobacter pylori infection impairs the expressions and functional activities of duodenal mucosal bicarbonate transport proteins, CFTR (show CFTR Antibodies) and SLC26A6, which contributes to the development of duodenal ulcer.
Molecular dynamics simulations of the STAS domains of rat prestin (show SLC26A5 Antibodies) and human pendrin (show SLC26A4 Antibodies) reveal conformational motions in conserved flexible regions.
Data show that SLC26A6 variants do not alter the risk for the development of chronic pancreatitis.
In the intestinal epithelium, PAT-1 (show APPBP2 Antibodies) (SLC26A6) could mediate apical oxalate influx or apical oxalate efflux depending on the magnitude and direction prevailing counterion driver gradients as well as the relative affinities of the transported anions.
orthologous mouse and human SLC26A6 proteins differ in anion selectivity, transport mechanism, and acute regulation, but both mediate electroneutral Cl(-)/HCO(3)(-) exchange
In human kidney SLC26A6 and A7 have a distinct, partially overlapping expression in distal segments of nephrons. The distribution partly differs from that found previously in rodent kidneys.
findings indicate that slc26a6 functions as a coupled 1Cl-/2HCO3- exchanger
Mouse Slc26a6 and human SLC26A6 each mediated electroneutral Cl-/HCO3- and Cl-/OH- exchange. But, whereas Cl-/oxalate exchange by mouse Slc26a6 was electrogenic, that mediated by human SLC26A6 appeared electroneutral.
No mutation was found in the coding regions and intron-exon boundaries of the genes for CA II (show CA2 Antibodies), CA IV (show CA4 Antibodies), CA XIV (show CA14 Antibodies), kNCB1, NHE3 (show SLC9A3 Antibodies), NHE8 (show SLC9A8 Antibodies), NHRF1, NHRF2 and SLC26A6 amplified from genomic DNA of family members with pRTA.
Slc26a6 is a unique cardiac electrogenic Cl(-)/HCO3(-) transporter in ventricular myocytes, which has roles in regulating pHi, excitability, and contractility.
This study showed that transepithelial sulfate fluxes across the mouse distal ileum demonstrating that DRA (and to a lesser extent, PAT1) secretes sulfate with significant implications for intestinal sulfate absorption and overall homeostasis.
Enzymatic deglycosylation of SLC26A6 expressed on the plasma membrane of intact cells strongly reduced oxalate transport activity.
Slc26a1 (show SLC26A1 Antibodies), Slc26a6 and Slc26a7 (show SLC26A7 Antibodies) are novel participants in the extracellular transport of bicarbonate during enamel maturation.
Results suggest that PAT1 (show APPBP2 Antibodies) slows down APP (show APP Antibodies) trafficking to the cell surface in primary cortical neurons
Both PAT-1 and DRA significantly contribute to intestinal fluid absorption and enterocyte acid/base balance but are activated by different ion gradients.
Cardiac myocytes express different isoforms of Slc26a6, which encode electrogenic Cl(-)/HCO3(-) and Cl(-)/oxalate exchangers.
Slc26a6-null mice exhibited increased renal and intestinal sodium-dependent succinate uptake, as well as urinary hyperoxaluria and hypocitraturia, but no change in urinary pH, indicating enhanced transport activity of NaDC-1 (show SLC13A2 Antibodies).
NMR and CE were used to characterize the urinary metabolome in slc26a6 null mice. Clear metabolic differentiation between the urinary profiles of the slc26a6 null and the wild type mice were observed using both methods.
SLC26A6 mediates 1:2 Cl-/HCO3- exchange, and the exchanger most probably upregulates SLC26A3 (show SLC26A3 Antibodies) in its absence, therefore mediating 2:1 exchange.
This gene belongs to the solute carrier 26 family, whose members encode anion transporter proteins. This particular family member encodes a protein involved in transporting chloride, oxalate, sulfate and bicarbonate. Several alternatively spliced transcript variants of this gene, encoding distinct isoforms, have been described, but the full-length nature of some of these variants has not been determined.
solute carrier family 26, member 6
, solute carrier family 26 member 6
, SLC26A6a anion exchanger
, anion transporter 1
, pendrin L1
, sulfate anion transporter