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Cat. No. ARG35251

KRT19 Knockout A2780 Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Ovary

  • Disease:

    Endometrioid carcinoma

The KRT19 Knockout A2780 Polyclonal Cells are a CRISPR/Cas9-edited polyclonal cell population from the A2780 ovarian cancer line, designed for KRT19 loss-of-function studies. KRT19 encodes an intermediate filament protein that partners with KRT8 and links cytoskeletal regulation to Rho GTPase, PI3K/AKT, and Wnt/beta-catenin signaling. Knockout disrupts keratin networks and may promote epithelial-mesenchymal transition, altering migration and invasion. These cells suit ovarian cancer metastasis, EMT, drug resistance, and biomarker studies. Common assays include western blot, immunofluorescence, wound healing, invasion, and co-IP to probe KRT19 interactions with beta-catenin and AKT.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    A2780

    Sex of Donor

    Female

    Age

    Unknown

    Derived From Site

    In situ; Ovary

    Gene Name

    KRT19

    Gene Identifier

    NCBI Gene ID 3880

    Morphology

    Epithelial-like

    Growth Mode

    Adherent and suspension

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    DMEM

    Supplement(s)

    10% Fetal Bovine Serum, 1% Penicillin-Streptomycin Solution

    Temperature

    37°C

    Atmosphere

    5% CO₂

  • Quality Control

    Sterility testing

    The bacterial, yeast, and fungi are not detected in these cells by daily monitor.

    Mycoplasma testing

    Negative for mycoplasma through PCR analysis

  • Disclaimer

    Intended Use

    This product is intended for laboratory in vitro use only. lt is not intended for diagnostic, therapeutic, or clinical applications.

    Disclaimer

    Ascent Research endeavors to provide accurate and up-to-date product information. However, no warranties or representations are made regarding its completeness or reliability. References to scientific literature and patents are for informational purposes only, and the customer assumes sole responsibility for verifying their accuracy.

    By accepting this product, the customer acknowledges and agrees to assume all risks associated with its receipt, handling, storage, disposal, and use, including compliance with all applicable safety and environmental regulations and precautions. Relevant laws, regulations, and ethical guidelines must be followed in conducting any research, modifications, or derivatives derived from this product.

    This product is provided "AS IS", and except as expressly stated herein, Ascent Research disclaims all other warranties, express or implied. Under no circumstances shall Ascent Research, its affiliates, or representatives be liable for indirect, incidental, consequential, or punitive damages arising from the use of this material. While Ascent Research employs rigorous quality control measures, we shall not be held responsible for damages resulting from misidentification or misinterpretation of the provided materials.

Description

The KRT19 Knockout A2780 Polyclonal Cells are a CRISPR/Cas9-edited polyclonal cell population for studying KRT19 loss in ovarian cancer. Generated from A2780 cells, this model pools cells with targeted disruptions in the KRT19 gene, encoding cytokeratin 19. The polyclonal format avoids clonal selection bias and provides a robust loss-of-function tool for cytoskeletal and signaling research.

A2780 is an epithelial ovarian carcinoma cell line established from an untreated patient, widely used for metastasis and drug resistance studies. These cells maintain epithelial characteristics and responsiveness to chemotherapeutics, making them a relevant host for investigating cytoskeletal gene function in a cancer context.

KRT19, a type I intermediate filament protein, heterodimerizes with KRT8 to form keratin networks essential for epithelial architecture. KRT19 interacts with beta-catenin, 14-3-3 proteins, PKC, and AKT, and its expression is regulated by transcription factors GATA3, FOXA1, SOX9, p63 and signals like EGF and TGF-beta. Downstream, KRT19 modulates E-cadherin, vimentin, and MMP expression, influencing beta-catenin/TCF/LEF activity. Its loss may disrupt RhoA-ROCK-LIMK-cofilin and PI3K/AKT/mTOR pathways, promoting cytoskeletal reorganization and EMT.

In A2780 cells, KRT19 knockout likely impairs keratin filament integrity, altering cell adhesion and morphology. This mimics EMT, marked by reduced E-cadherin and increased vimentin, potentially enhancing migration and invasion. The model enables dissection of how cytoskeletal disruption impacts ovarian cancer progression, circulating tumor cell biology, and apoptosis resistance, particularly through cross-talk with Wnt and PI3K/AKT signaling.

Applications include western blotting, RT-qPCR, immunofluorescence, wound healing, and Transwell invasion assays to study migration and invasion. Flow cytometry, caspase activity assays, and MTT assays facilitate apoptosis and drug resistance studies. Co-immunoprecipitation and RNA-seq can probe protein interactions and transcriptomic changes. This product supports EMT research, biomarker validation, and mechanistic cancer studies. For further information, contact Ascent Research.

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