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anti-Claudin 19 (CLDN19) Antibodies

The product of CLDN19 belongs to the claudin family. Additionally we are shipping Claudin 19 Kits (20) and Claudin 19 Proteins (6) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
CLDN19 149461 Q8N6F1
CLDN19 298487 Q5QT56
CLDN19 242653 Q9ET38
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Top anti-Claudin 19 Antibodies at antibodies-online.com

Showing 10 out of 34 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Cow Rabbit Un-conjugated WB 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated ELISA, WB Western blot analysis of extracts from Jurkat/HepG2 cells, using CLDN19 Antibody. The lane on the right is treated with the synthesized peptide. 100 μg Log in to see 2 to 3 Days
$302.50
Details
Human Rabbit Un-conjugated ELISA, WB 100 μL Log in to see 8 to 10 Days
$478.50
Details
Cow Rabbit Un-conjugated WB Western blot analysis of Claudin 19 expression in MCF7 (A), HepG2 (B) whole cell lysates. 200 μL Log in to see 9 Days
$487.50
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Un-conjugated IF (p), IHC (p), WB Formalin-fixed and paraffin embedded mouse stomach tissue labeled with Anti-Claudin 19 Polyclonal Antibody, Unconjugated (ABIN2173171) at 1:200 followed by conjugation to the secondary antibody and DAB staining 100 μL Log in to see 14 to 21 Days
$269.50
Details
Human Rabbit Un-conjugated ELISA, WB 100 μg Log in to see 11 to 16 Days
$412.86
Details
Human Rabbit Un-conjugated ELISA, WB 100 μL Log in to see 14 Days
$201.19
Details
Human Rabbit Alexa Fluor 350 IF (p)   100 μL Log in to see 3 to 7 Days
$357.50
Details
Human Rabbit Alexa Fluor 488 IF (p)   100 μL Log in to see 3 to 7 Days
$357.50
Details

CLDN19 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
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Top referenced anti-Claudin 19 Antibodies

  1. Cow (Bovine) Polyclonal CLDN19 Primary Antibody for WB - ABIN2778043 : Konrad, Schaller, Seelow, Pandey, Waldegger, Lesslauer, Vitzthum, Suzuki, Luk, Becker, Schlingmann, Schmid, Rodriguez-Soriano, Ariceta, Cano, Enriquez, Juppner, Bakkaloglu, Hediger, Gallati, Neuhauss, Nurnberg, Weber: Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. in American journal of human genetics 2006 (PubMed)

More Antibodies against Claudin 19 Interaction Partners

Human Claudin 19 (CLDN19) interaction partners

  1. CLDN19 genetic mutation is responsible for familial magnesium deficiency with hypercalciuria and nephrocalcinosis.

  2. analysis of a novel mutation c.241C>T in exon 2 of CLDN19 in a Chinese patient

  3. Claudin-19, the most abundant claudin in myelin, exhibited no binding to ZO2 (show TJP2 Antibodies) protein.

  4. patients with CLDN19 mutations have a high risk of progression to chronic renal disease

  5. Case Reports: novel CLDN19 mutation in familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

  6. The risk of end-stage renal disease in patients with CLDN19 mutations was two times the risk of patients with CLDN16 (show CLDN16 Antibodies) mutations. Ocular abnormalities were observed only in patients with CLDN19 mutations.

  7. In a patient with consanguineous parents, history of disturbed organization and development of the retina, a diagnosis of Familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by claudin-19 mutation should be considered.

  8. Ocular manifestations and exercise intolerance mimicking mild to moderate periodic paralysis are two symptoms that may occur in patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis and may indicate CLDN19 mutations.

  9. The identification of CLDN19 mutations in patients with chronic renal failure and severe visual impairment supports the fundamental role of claudin-19 for normal renal tubular function and undisturbed organization and development of the retina.

Mouse (Murine) Claudin 19 (CLDN19) interaction partners

  1. this study presents the structure of mammalian claudin-19 in complex with C-CPE (show CPE Antibodies) at 3.7 A resolution.

  2. Sp1 (show SP1 Antibodies) site is crucial for Cldn19 gene expression in kidney cells.

  3. Claudin-16 (show CLDN16 Antibodies) and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium.

Claudin 19 (CLDN19) Antigen Profile

Protein Summary

The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene.

Gene names and symbols associated with anti-Claudin 19 (CLDN19) Antibodies

  • claudin 19 (cldn19) antibody
  • claudin 19 (CLDN19) antibody
  • claudin 19 (LOC100357396) antibody
  • claudin 19 (Cldn19) antibody
  • claudin-19 antibody
  • HOMG5 antibody
  • zgc:112141 antibody

Protein level used designations for anti-Claudin 19 (CLDN19) Antibodies

claudin-19 , claudin 19

GENE ID SPECIES
496231 Xenopus laevis
550431 Danio rerio
697807 Macaca mulatta
747192 Pan troglodytes
100032684 Monodelphis domestica
100053591 Equus caballus
100357396 Oryctolagus cuniculus
149461 Homo sapiens
298487 Rattus norvegicus
607005 Canis lupus familiaris
100294682 Sus scrofa
513034 Bos taurus
242653 Mus musculus
101102362 Ovis aries
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