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Cat. No. ARG34269

ITM2B Knockout A549 Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Lung

  • Disease:

    Lung adenocarcinoma

CRISPR/Cas9-edited polyclonal ITM2B knockout cells derived from the A-549 human lung adenocarcinoma line. ITM2B (BRI2) modulates gamma-secretase activity and amyloid precursor protein (APP) processing by interacting with the gamma-secretase complex, including presenilin-1 (PSEN1), thereby influencing amyloid-beta generation and Notch signaling. This model enables study of neurodegeneration-linked pathways and cancer cell migration in a lung cancer background. Ideal for investigating gamma-secretase regulation, Notch signaling, and cell adhesion/migration. Applicable techniques include gamma-secretase activity assays, amyloid-beta ELISA, co-immunoprecipitation, and invasion assays. Please contact Ascent Research for further details.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    A549

    Sex of Donor

    Male

    Age

    58 years

    Derived From Site

    Lung

    Gene Name

    ITM2B

    Gene Identifier

    NCBI Gene ID 9445

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    MEM

    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

ITM2B Knockout A-549 Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout population derived from A-549 human lung adenocarcinoma cells. This product features targeted disruption of the ITM2B (BRI2) gene, generating a loss-of-function model suitable for investigating ITM2B-dependent processes. The polyclonal format provides a heterogeneous pool of edited genes for bulk assays without clonal bias.

A-549 cells, established from lung adenocarcinoma tissue, represent a widely used type II alveolar epithelial model. These cells retain malignant properties, including rapid proliferation, migration, and invasion, while maintaining key epithelial characteristics. Their well-studied genome and relevance to non-small cell lung cancer make them an optimal platform for genetic perturbation studies, particularly for interrogating pathways involved in tumorigenesis and metastasis.

ITM2B encodes a type II transmembrane protein cleaved by furin and ADAM10, releasing a secreted fragment that interacts with APP and regulates the gamma-secretase complex composed of PSEN1, PSEN2, nicastrin, APH-1, and PEN-2. Through this interaction, ITM2B modulates amyloid-beta production and Notch receptor processing, influencing NICD-mediated transcription. Additionally, ITM2B is implicated in cell adhesion and migration, connecting it to both neurodegeneration and cancer phenotypes.

In the A-549 background, ITM2B knockout enables dissection of gamma-secretase activity and Notch signaling within a cancer-relevant context. While ITM2B is traditionally associated with Alzheimer??s and familial dementias, its impact on cell migration and adhesion suggests roles in metastatic progression. This model thus bridges neurobiology and oncology, allowing researchers to examine how a neuroprotective factor affects lung adenocarcinoma behavior.

Typical applications include gamma-secretase activity assays using APP or Notch substrates, amyloid-beta ELISA, co-immunoprecipitation with gamma-secretase components, and cell migration/invasion analyses. Researchers can also perform western blotting and RT-qPCR for knockout validation, as well as Notch reporter assays. For custom inquiries or additional product details, please contact Ascent Research.

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