Claudin-16 Antibody

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Product Details

Summary
Product Discontinued
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Order Details


    • Catalog Number
      H00010686-A01
    • Availability
      Product Discontinued

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Claudin-16 Antibody Summary

Immunogen
CLDN16 (NP_006571, 1 a.a. ~ 74 a.a) partial recombinant protein with GST tag.MTSRTPLLVTACLYYSYCNSRHLQQGVRKSKRPVFSHCQVPETQKTDTRHLSGARAGVCPCCHPDGLLATMRD
Specificity
CLDN16 - claudin 16
Clonality
Polyclonal
Host
Mouse
Gene
CLDN16
Purity
Unpurified
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Applications/Dilutions

Dilutions
  • ELISA
  • Western Blot 1:500
Application Notes
Antibody reactive against cell lysate and recombinant protein for western blot. It has also been used for ELISA.

Reactivity Notes

Human. Other species not tested.

Packaging, Storage & Formulations

Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
Unpurified antisera so the specific antibody concentration is unknown. Contains 50% glycerol.
Preservative
No Preservative
Purity
Unpurified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for Claudin-16 Antibody

  • claudin 16
  • Claudin16
  • Claudin-16
  • CLDN16
  • HOMG3
  • HOMG3paracellin-1
  • Paracellin-1
  • PCLN1
  • PCLN-1
  • PCLN1hypomagnesemia 3, with hypercalciuria and nephrocalcinosis

Background

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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Bioinformatics

Gene Symbol CLDN16
Entrez
OMIM
Uniprot