Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The protein encoded by CLCNKB is a member of the family of voltage-gated chloride channels. Additionally we are shipping CLCNKB Proteins (4) and many more products for this protein.
Showing 10 out of 47 products:
Human Polyclonal CLCNKB Primary Antibody for EIA, WB - ABIN951557
Yu, Xu, Pan, Ren, Wang, Meng, Huang, Chen: Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome. in Clinical genetics 2010
Show all 4 references for ABIN951557
Cow (Bovine) Polyclonal CLCNKB Primary Antibody for WB - ABIN2776082
Strausberg, Feingold, Grouse, Derge, Klausner, Collins, Wagner, Shenmen, Schuler, Altschul, Zeeberg, Buetow, Schaefer, Bhat, Hopkins, Jordan, Moore, Max, Wang, Hsieh, Diatchenko, Marusina, Farmer et al.: Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. ... in Proceedings of the National Academy of Sciences of the United States of America 2002
Cow (Bovine) Polyclonal CLCNKB Primary Antibody for WB - ABIN2776083
Gorgojo, Donnay, Jeck, Konrad: A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult age. in Hormone research 2006
IGF-1 (show IGF1 Antibodies), by stimulating ClC-K2 channels, promotes net Na(+) and Cl(-) reabsorption, thus reducing driving force for potassium secretion by the cortical collecting duct.
Single loci of tag Single Nucleotide Polymorphisms of CLCNKA_B are not enough to increase the Essential Hypertension susceptibility, the combination of CLCNKA (show CLCNKA Antibodies) SNP, salt, marine products, meat, edible oil consumption is associated with elevated risk
results demonstrate that the carboxyl terminus of hClC-Kb is not part of the binding site for barttin (show BSND Antibodies), but functionally modifies the interplay with barttin (show BSND Antibodies).
These results demonstrate that mutations in a cluster of hydrophobic residues within transmembrane domain 1 affect barttin (show BSND Antibodies)-CLC-K interaction and impair gating modification by the accessory subunit
we report here for the first time that ClC-Kb disease-causing mutations located around the selectivity filter can result in both reduced surface expression and hyperactivity in heterologous expression systems
Case Report: 2 mutations in the CLCNKB gene, leading to a molecular diagnosis of Bartter syndrome type III in case of sudden infant death.
R8W and G47R, two naturally occurring barttin (show BSND Antibodies) mutations identified in patients with Bartter syndrome type IV, reduce barttin (show BSND Antibodies) palmitoylation and CLC-K/barttin (show BSND Antibodies) channel activity.
HEK293 cells the potentiating effect of niflumic acid (NFA) on CLC-Ka/barttin (show BSND Antibodies) and CLC-Kb/barttin (show BSND Antibodies) channels seems to be absent while the blocking efficacy of niflumic acid and benzofuran derivatives observed in oocytes is preserved
study investigated the functional consequences of seven mutations; four mutants carried no current whereas others displayed a 30-60 percent reduction in conductance as compared with wild-type ClC-Kb
expands the association between CLCNKB and essential hypertension to a non-European ancestry population
This article presents the case of a patient with hypokalaemia caused by CLCNKB gene mutation hard to categorise as GS or BS type 3.
The open probability and mean open time of ClC-2 (show CLCN2 Antibodies) was voltage dependent, decreasing dramatically as the patches were depolarized. ClC-2 (show CLCN2 Antibodies) is uniquely suitable to promote anion secretion with little anion reabsorption.
The protein encoded by this gene is a member of the family of voltage-gated chloride channels. Chloride channels have several functions, including the regulation of cell volume, membrane potential stabilization, signal transduction and transepithelial transport. This gene is expressed predominantly in the kidney and may be important for renal salt reabsorption. Mutations in this gene are associated with autosomal recessive Bartter syndrome type 3 (BS3). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
chloride channel Kb
, chloride channel Ka
, chloride channel protein ClC-Kb-like
, chloride channel K1-like; putative basolateral cTAL chloride channel ClC-Ka
, chloride channel protein ClC-Kb
, putative basolateral mTAL chloride channel ClC-Ka
, Chloride channel protein ClC-Kb
, chloride channel protein ClC-Ka
, chloride channel, kidney, B
, chloride channel K2