Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. Additionally we are shipping Claudin 16 Kits (15) and Claudin 16 Proteins (4) and many more products for this protein.
Showing 10 out of 60 products:
Human Polyclonal CLDN16 Primary Antibody for EIA, FACS - ABIN951545
Kuo, Chien, Lin, Chan, Tsai, Chen: Significant elevation of CLDN16 and HAPLN3 gene expression in human breast cancer. in Oncology reports 2010
Show all 4 references for ABIN951545
Human Polyclonal CLDN16 Primary Antibody for WB - ABIN2778049
Müller, Kausalya, Claverie-Martin, Meij, Eggert, Garcia-Nieto, Hunziker: A novel claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting. in American journal of human genetics 2003
Show all 3 references for ABIN2778049
detected a novel mutation in CLDN16 for the first time. The clinical and genetic findings from this study will help to expand the understanding of this rare disease, FHHNC
claudin-16 gene (CLDN16) mutations result in amelogenesis imperfect.
CLDN16 mutations are associated with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.
1,25(OH)2 VitD transcriptionally inhibits renal claudin-16 expression by a mechanism sensitive to CaSR (show CASR Antibodies) and Mg(2 (show MUC7 Antibodies)+).
A novel CLDN16 mutation has been identified in a large consanguineous family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.
These results suggest that STX8 (show STX8 Antibodies) mediates the recycling of CLDN16 and constitutes an important component of the CLDN16 trafficking machinery in the kidney.
Six different mutations of CLDN16 were detected (five missense and one nonsense); three of the missense mutations were previously unknown (p.Cys80Tyr, p.Lys183Glu, and p.Gly233Arg).
A novel mutation of CLDN16 gene is responsible for familial hypomagnesaemia in Turkish children.
Claudin-16 plays a role beyond that of an initial metastasis repressor in breast cancer.
Claudin 16 gene revealed homozygosity for the p.K183E(AAA (show APP Antibodies)>GAA (show GAA Antibodies)) C. 547A>G indicating the diagnosis of hypomagnesemia with hypercalciuria and nephrocalcinosis.
Claudin-16 sequences were not usually amplified from a small number of sperm cells (< or =10 cells) but claudin-16 DNA sequences were occasionally detected when a large number of sperm cells (> or =50 cells) were present.
Renal lesions in Japanese Black cattle are not necessarily associated with homozygous deletion of the CL-16 gene.
1,25(OH)2 VitD transcriptionally inhibits renal claudin-16 expression by a mechanism sensitive to CaSR (show CASR Antibodies) and Mg(2 (show MCOLN1 Antibodies)+).
Mg(2 (show MCOLN1 Antibodies)+)-loaded animals displayed hypermagnesemia with increasing urine Mg(2 (show MCOLN1 Antibodies)+)/Ca(2 (show CA2 Antibodies)+) levels paralleled by a decrease in claudin-16 protein and mRNA in the kidney.
data suggest that claudin-16 forms a non-selective paracellular cation channel (show TRPV1 Antibodies), rather than a selective Mg(2 (show MCOLN1 Antibodies)+)/Ca(2 (show CA2 Antibodies)+) channel as previously proposed
Perturbation in salt and acid-base metabolism in CLDN16 knockout mice has its origin in the defective cation permeability selectivity of the thick ascending limb of the nephron.
Insights into driving forces and paracellular permeability from claudin-16 knockdown mouse
Claudin-16 and claudin-19 (show CLDN19 Antibodies) interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium.
Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is found primarily in the kidneys, specifically in the thick ascending limb of Henle, where it acts as either an intercellular pore or ion concentration sensor to regulate the paracellular resorption of magnesium ions. Defects in this gene are a cause of primary hypomagnesemia, which is characterized by massive renal magnesium wasting with hypomagnesemia and hypercalciuria, resulting in nephrocalcinosis and renal failure. This gene and the CLDN1 gene are clustered on chromosome 3q28.
, hypomagnesemia 3, with hypercalciuria and nephrocalcinosis
, H59D2a protein