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Cat. No. ARG35908

ASGR1 Knockout CaSki Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Uterus (cervix)

  • Disease:

    Squamous cell carcinoma

The ASGR1 Knockout Ca Ski Polyclonal Cells provide a CRISPR/Cas9-edited polyclonal knockout population of human cervical carcinoma epithelial cells, enabling loss-of-function studies of the asialoglycoprotein receptor 1 (ASGR1). ASGR1 mediates clathrin-dependent endocytosis and may modulate JAK2/STAT3 signaling, relevant to cervical cancer biology. This model is designed for investigating ASGR1 function in glycoprotein metabolism, receptor-mediated endocytosis, and intracellular signaling. Researchers can employ western blotting, flow cytometry, endocytosis assays, and functional assays to explore its role in cell proliferation, apoptosis, migration, and ligand-based drug targeting.

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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

    ASGR1

    Gene Identifier

    NCBI Gene ID 432

    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 ASGR1 Knockout Ca Ski Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout cell population designed to disrupt the ASGR1 gene in the human cervical carcinoma cell line Ca Ski. This product provides a robust loss-of-function model to investigate the role of the asialoglycoprotein receptor 1 (ASGR1) in endocytosis, glycoprotein metabolism, and signaling. As a polyclonal knockout pool, cells harbor heterogeneous disruptions enabling pooled functional studies.

Ca Ski is a human cervical carcinoma epithelial line derived from a metastatic squamous cell carcinoma, containing integrated HPV16 DNA with constitutive E6/E7 expression. It is a widely used model for cervical cancer research, including viral oncoprotein function, epithelial carcinogenesis, and HPV-driven pathways. The epithelial origin and malignant phenotype make it a relevant host for studying genes influencing tumor cell behavior, adhesion, and immune modulation.

ASGR1 encodes the major subunit of the asialoglycoprotein receptor, which forms hetero-oligomers with ASGR2 to mediate clathrin-dependent endocytosis of desialylated glycoproteins via interactions with adaptor AP2 and clathrin. In non-hepatic cells, ASGR1 may engage JAK2/STAT3 signaling downstream of IL-6 and upstream regulators HNF4A, CEBPA, and STAT3, influencing NFKB1 and lysosomal enzyme expression. This positions ASGR1 at the intersection of receptor-mediated endocytosis and proliferative/survival pathways.

The functional role of ASGR1 in cervical cancer is not well established, making this knockout model valuable. Its depletion may affect cell adhesion and immune-related interactions, especially given ASGR1’s links to NF-??B and JAK-STAT pathways frequently altered in HPV-driven cancers. This model enables investigation of cross-talk between HPV oncoproteins and the host endocytic machinery, potentially revealing new targets.

Key applications include western blotting, RT-qPCR, immunofluorescence, and flow cytometry for confirming ASGR1 disruption and surface expression. Researchers can perform endocytosis assays with fluorescent asialoorosomucoid, proliferation, apoptosis, and migration assays, and co-immunoprecipitation for ASGR1?CASGR2 interactions. This product supports studies in glycobiology, cancer biology, and drug targeting. For further information, contact Ascent Research.

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