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  • mProX™ Human CLDN3 Stable Cell Line

    [CAT#: S01YF-1023-PY263]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:

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    Product Information

    Target Family
    Other Targets
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;Huh-7;HepG2
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    Cancer Research
    Related Diseases
    Papillary Carcinoma; Williams-Beuren Syndrome
    Gene ID
    Human:1365
    UniProt ID
    Human:O15551

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    CLDN3, a member of the claudin family of tight junction proteins, has been studied in various contexts. One study investigated the impact of chronic exposure to arsenate through drinking water on the intestinal barrier and found that chronic exposure to As(V) affects the expression of CLDN3, among other proteins, leading to increased paracellular permeability and endotoxemia. Another study focused on the role of CLDN3 in regulating epithelial tight junction architecture. It was found that CLDN23, in association with CLDN3 and CLDN4, reshapes tight junctions and regulates barrier function. Additionally, CLDN3 has been studied in the context of fructans, where it was found that specific fructans can protect the expression of CLDN3 and other tight junction genes, contributing to gut homeostasis. Lastly, CLDN3 was examined in pulmonary adenoid cystic carcinoma and mucoepidermoid carcinoma, where overexpression of CLDN3 was observed. These studies highlight the diverse applications of CLDN3 in understanding intestinal barrier function, tight junction architecture, and disease pathology.

    Protocols

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    FAQ

    chat Skyler Johnson (Verified Customer)

    What is the significance of CLDN3 overexpression in ovarian cancer? Apr 22 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Overexpression of CLDN3 in ovarian cancer promotes cellular viability, migration, and invasion, suggesting that targeting CLDN3 could provide new therapeutic opportunities. Apr 22 2023

    chat Jordan Williams (Verified Customer)

    How does CLDN3 expression affect breast cancer? May 04 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Loss of CLDN3 expression in breast cancer cells may play a role in invasion and metastasis, indicating its potential as a biomarker for cancer progression. May 04 2021

    Published Data

    Fig.1 Overexpression of CLDN3 in HCC cell lines.

    Confirmation of CLDN3 ectopic expression in HCC cell lines (HepG2 and Huh-7) through western blot analysis was carried out.

    Ref: Jiang, Lei, et al. "CLDN3 inhibits cancer aggressiveness via Wnt-EMT signaling and is a potential prognostic biomarker for hepatocellular carcinoma." Oncotarget 5.17 (2014): 7663.

    Pubmed: 25277196

    DOI: 10.18632/oncotarget.2288

    Research Highlights

    Domene, Adri√°n. et al. "Impact of Chronic Exposure to Arsenate through Drinking Water on the Intestinal Barrier." Chemical research in toxicology, 2023.
    Chronic exposure to inorganic arsenic, specifically As(III) and As(V), has been found to increase the risk of certain types of cancer and other non-carcinogenic conditions in a significant portion of the population. While the primary route of exposure is through oral ingestion, it has been noted that children may be at a heightened risk due to their vulnerability. This issue affects millions of individuals worldwide.
    Domene, Adri√°n. et al. "Impact of Chronic Exposure to Arsenate through Drinking Water on the Intestinal Barrier." Chemical research in toxicology, 2023.
    Pubmed: 37819996   DOI: 10.1021/acs.chemrestox.3c00201

    Raya-Sandino, Arturo. et al. "Claudin-23 reshapes epithelial tight junction architecture to regulate barrier function." Nature communications, 2023.
    It is shown that CLDN23 is highly expressed in luminal intestinal epithelial cells and plays a crucial role in strengthening the barrier. The study also reveals that CLDN23 interacts with CLDN3 and CLDN4 to regulate paracellular ion and macromolecule permeability. Computational modeling suggests that CLDN23 forms heteromeric and heterotypic complexes with unique pore architecture and overall net charge. These findings shed light on the organization of tight junctions and propose a model wherein different claudins form distinct complexes to modify epithelial barrier function.
    Raya-Sandino, Arturo. et al. "Claudin-23 reshapes epithelial tight junction architecture to regulate barrier function." Nature communications, 2023.
    Pubmed: 37798277   DOI: 10.1038/s41467-023-41999-9

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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