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Browse our Claudin 16 (CLDN16) ELISA Kits

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Claudin 16 ELISA Kits (CLDN16)
On www.antibodies-online.com are 15 Claudin 16 (CLDN16) ELISA Kits from 4 different suppliers available. Additionally we are shipping Claudin 16 Antibodies (59) and Claudin 16 Proteins (4) and many more products for this protein. A total of 81 Claudin 16 products are currently listed.
Synonyms:
claudin-16, CLDN16, HOMG3, Pcln1
list all ELISA KIts Gene Name GeneID UniProt
CLDN16 10686 Q9Y5I7
CLDN16 114141 Q925N4
CLDN16 155268 Q91Y55

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More ELISA Kits for Claudin 16 Interaction Partners

Human Claudin 16 (CLDN16) interaction partners

  1. 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

  2. claudin-16 gene (CLDN16) mutations result in amelogenesis imperfect.

  3. CLDN16 mutations are associated with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.

  4. 1,25(OH)2 VitD transcriptionally inhibits renal claudin-16 expression by a mechanism sensitive to CaSR (show CASR ELISA Kits) and Mg(2 (show MUC7 ELISA Kits)+).

  5. A novel CLDN16 mutation has been identified in a large consanguineous family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.

  6. These results suggest that STX8 (show STX8 ELISA Kits) mediates the recycling of CLDN16 and constitutes an important component of the CLDN16 trafficking machinery in the kidney.

  7. 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).

  8. A novel mutation of CLDN16 gene is responsible for familial hypomagnesaemia in Turkish children.

  9. Claudin-16 plays a role beyond that of an initial metastasis repressor in breast cancer.

  10. Claudin 16 gene revealed homozygosity for the p.K183E(AAA (show APP ELISA Kits)>GAA (show GAA ELISA Kits)) C. 547A>G indicating the diagnosis of hypomagnesemia with hypercalciuria and nephrocalcinosis.

Cow (Bovine) Claudin 16 (CLDN16) interaction partners

  1. 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.

  2. Renal lesions in Japanese Black cattle are not necessarily associated with homozygous deletion of the CL-16 gene.

Mouse (Murine) Claudin 16 (CLDN16) interaction partners

  1. claudin-16 gene (CLDN16) mutations result in amelogenesis imperfect.

  2. 1,25(OH)2 VitD transcriptionally inhibits renal claudin-16 expression by a mechanism sensitive to CaSR (show CASR ELISA Kits) and Mg(2 (show MCOLN1 ELISA Kits)+).

  3. Mg(2 (show MCOLN1 ELISA Kits)+)-loaded animals displayed hypermagnesemia with increasing urine Mg(2 (show MCOLN1 ELISA Kits)+)/Ca(2 (show CA2 ELISA Kits)+) levels paralleled by a decrease in claudin-16 protein and mRNA in the kidney.

  4. data suggest that claudin-16 forms a non-selective paracellular cation channel (show TRPV1 ELISA Kits), rather than a selective Mg(2 (show MCOLN1 ELISA Kits)+)/Ca(2 (show CA2 ELISA Kits)+) channel as previously proposed

  5. 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.

  6. Insights into driving forces and paracellular permeability from claudin-16 knockdown mouse

  7. Claudin-16 and claudin-19 (show CLDN19 ELISA Kits) interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium.

Claudin 16 (CLDN16) Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with Claudin 16 (CLDN16)

  • claudin 16 (CLDN16) Elisa Kit
  • claudin 16 (Cldn16) Elisa Kit
  • claudin 16 (LOC100356384) Elisa Kit
  • claudin-16 Elisa Kit
  • CLDN16 Elisa Kit
  • HOMG3 Elisa Kit
  • Pcln1 Elisa Kit

Protein level used designations for Claudin 16 (CLDN16) ELISA Kits

claudin 16 , PCLN-1 , claudin-16 , hypomagnesemia 3, with hypercalciuria and nephrocalcinosis , paracellin-1 , CL-16 , H59D2a protein

GENE ID SPECIES
429147 Gallus gallus
740268 Pan troglodytes
10686 Homo sapiens
608218 Canis lupus familiaris
100302019 Sus scrofa
282184 Bos taurus
114141 Mus musculus
155268 Rattus norvegicus
100356384 Oryctolagus cuniculus
101105382 Ovis aries
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