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Cat. No. ARG35946

IL27 Knockout CaSki Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Uterus (cervix)

  • Disease:

    Squamous cell carcinoma

The IL27 Knockout Ca Ski Polyclonal Cells comprise a CRISPR?Cas9?edited polyclonal population of Ca Ski cervical carcinoma cells (HPV?16?positive) with targeted disruption of the IL27 gene. This model ablates expression of the IL?27 alpha subunit (p28), preventing formation of the functional IL?27 heterodimer with EBI3, and allows investigation of IL?27?dependent signaling in a clinically relevant epithelial context. IL?27 normally signals through IL?27RA/gp130, activating JAK1?CSTAT1/STAT3 cascades to modulate T?cell differentiation and inflammation. The knockout cells are designed for studying IL?27 biology in cervical cancer immunology, including cytokine profiling, phospho?STAT analysis, T?cell co?cultures, and drug screening, facilitating research on immune checkpoint regulation and HPV?driven oncogenesis.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    CaSki

    Sex of Donor

    Female

    Age

    40 years

    Derived From Site

    Metastatic; Small intestine

    Gene Name

    IL27

    Gene Identifier

    NCBI Gene ID 246778

    Morphology

    Epithelial-like

    Growth Mode

    Adherent

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    RPMI 1640

    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 IL27 Knockout Ca Ski Polyclonal Cells are a CRISPR/Cas9?edited cell population generated from the Ca Ski human cervical carcinoma cell line, featuring targeted disruption of the IL27 gene. Supplied as a polyclonal pool, this model enables loss?of?function interrogation without clonal selection, facilitating robust studies of IL?27?dependent processes. The knockout eliminates the p28 subunit required for assembly of the functional IL?27 cytokine, thereby abrogating downstream signaling initiated by the IL?27 heterodimer.

The Ca Ski cell line is an epithelial, HPV?16?positive cervical carcinoma model originally derived from an epidermoid carcinoma metastasis. Extensively used in HPV oncogenesis research, Ca Ski cells retain integrated HPV?16 genomes and express viral oncoproteins E6 and E7, providing a clinically relevant context for investigating cytokine networks that intersect with viral transformation and immune escape.

IL27 encodes the IL?27 alpha subunit (p28), which partners with EBI3 to form the IL?27 heterodimeric cytokine. Secreted IL?27 binds a receptor complex of IL?27RA (WSX?1/TCCR) and gp130, triggering JAK1/JAK2?mediated phosphorylation of STAT1 and STAT3. Upstream activators include TLR agonists, IFN???, TNF???, and IL?1??, while downstream targets encompass SOCS1, SOCS3, T?bet, and IL?10. Through this pathway, IL?27 exerts context?dependent control over T?cell differentiation, inflammation, and immune regulation.

In the Ca Ski background, IL?27 signaling contributes to the modulation of the tumor microenvironment, potentially influencing immune surveillance and tumor progression. Disruption of IL27 permits dissection of how HPV?16 oncoproteins coordinate with IL?27?mediated STAT1/STAT3 activation to regulate checkpoint molecules, inflammatory mediators, and cellular functions such as migration and apoptosis. This knockout system thus offers a powerful model to explore the interplay between viral pathogenesis and IL?27 biology.

Applications include cytokine/chemokine profiling, phospho?STAT1/STAT3 flow cytometry, RT?qPCR analysis of IL?27 target genes, immune cell co?cultures, and migration/invasion assays. The polyclonal pool is also suitable for RNA?seq transcriptomic profiling and compound screening targeting the IL?27 pathway. For further technical information, please contact Ascent Research.

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