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Cat. No. ARG37723

C1orf159 Knockout HEK293T Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Kidney

C1orf159 Knockout HEK293T Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout cell population targeting the uncharacterized transmembrane protein C1orf159 in HEK293T human embryonic kidney cells. This loss-of-function model enables functional studies of C1orf159??s potential roles in intracellular signaling or metabolism, despite the absence of known interacting factors. Ideal for functional genomics, phenotypic screening, and drug target validation, the polyclonal format supports assays such as RNA-seq, proliferation, and co?immunoprecipitation. These cells offer a cost-effective discovery tool for researchers investigating novel gene functions in a widely used cellular background. Contact Ascent Research for additional details.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    HEK293T

    Sex of Donor

    Female

    Age

    Fetus

    Derived From Site

    Fetal kidney

    Gene Name

    C1orf159

    Gene Identifier

    NCBI Gene ID 54991

    Growth Mode

    Adherent

    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

C1orf159 Knockout HEK293T Polyclonal Cells consist of a CRISPR/Cas9-edited polyclonal knockout cell population targeting the C1orf159 gene in HEK293T cells. C1orf159 encodes a predicted transmembrane protein with unknown function. The polyclonal format ensures robust gene disruption across a heterogeneous cell pool, creating a loss-of-function model suitable for functional genomics without single-cell cloning. This approach retains natural population diversity while ablating C1orf159 expression, enabling comparative analyses against wild-type controls.

HEK293T cells, derived from human embryonic kidney cells, stably express the SV40 large T antigen, which permits episomal replication of plasmids containing the SV40 origin. This feature makes them a preferred host for high-level transient protein expression and lentiviral/retroviral vector production. Widely adopted across cell biology, HEK293T cells are valued for high transfectability, rapid growth, and broad experimental versatility, serving as a standard model for signaling, protein interaction, and functional genomics studies.

The biological function of C1orf159 is unclear; domain analysis predicts a multi-pass transmembrane protein, hinting at roles in intracellular signaling or metabolism. Currently, no upstream regulators, downstream effectors, or interacting proteins have been experimentally validated. The CRISPR/Cas9-mediated disruption in this polyclonal knockout pool creates a potent loss-of-function tool to probe C1orf159??s involvement in processes like proliferation, migration, or signal transduction. These cells enable discovery-driven phenotypic profiling and interactome studies, offering a path to delineate C1orf159??s molecular partners for the first time.

Using HEK293T as the genetic background leverages the line??s robust growth and ease of manipulation for high-throughput assays. Pairing an uncharacterized target with this well-defined host provides a clean system to attribute phenotypic changes directly to C1orf159 loss. Moreover, HEK293T??s prominent role in protein production and viral packaging allows assessment of whether C1orf159 affects heterologous protein yield or viral life cycle steps, extending the model??s utility beyond basic biology toward translational research.

Researchers can employ these polyclonal knockout cells in diverse applications, including RNA-seq, quantitative RT?PCR, Western blotting, immunofluorescence, and flow cytometry. Functional assays measuring proliferation, migration, invasion, or co?immunoprecipitation are readily supported. The polyclonal format is ideal for CRISPR-based genetic screens, drug target validation in cancer biology, and functional characterization of uncharacterized genes. The C1orf159 Knockout HEK293T Polyclonal Cells thus represent a cost-effective, scalable resource for the biomedical community. For additional information or custom inquiries, please contact Ascent Research.

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