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Cat. No. ARG1541

PAK4 Knockout Raji Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Bone

  • Disease:

    Burkitt lymphoma

The PAK4 Knockout Raji Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout population in the Raji B lymphocyte suspension line, enabling loss-of-function studies of the serine/threonine kinase PAK4. PAK4 functions downstream of Cdc42 and Rac1 to regulate cytoskeletal dynamics, proliferation, and survival via LIMK1/cofilin and ERK/AKT pathways, and is implicated in B-cell lymphomagenesis and therapy resistance. This product is suitable for signaling dissection, drug discovery, and functional genomics applications using assays such as Western blot, proliferation, migration, and reporter gene analysis in the context of Burkitt lymphoma-derived cells.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    Raji

    Cell Type

    B cell line

    Sex of Donor

    Male

    Age

    11 years

    Derived From Site

    In situ; Maxilla

    Gene Name

    PAK4

    Gene Identifier

    NCBI Gene ID 10298

    Morphology

    Lymphoblast-like

    Growth Mode

    Suspension

    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% COâ‚‚

  • 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. It 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 PAK4 Knockout Raji Polyclonal Cells comprise a CRISPR/Cas9-edited polyclonal knockout cell population with targeted disruption of the PAK4 gene in Raji B lymphocytes. This mixed population provides a loss-of-function model for studying PAK4-dependent mechanisms without clonal selection artifacts, and is well-suited for pooled functional screens and robust signaling analyses.

Raji cells are an EBV-positive B lymphoblastoid line derived from a Burkitt lymphoma patient, widely used as a model for B-cell malignancies. They retain characteristics of mature B lymphocytes and support investigation of B-cell receptor signaling, lymphomagenesis, and therapeutic responses, making them an ideal host for gene-editing studies.

PAK4 is a serine/threonine kinase acting downstream of the Rho GTPases Cdc42 and Rac1, which are activated by upstream signals such as HGF, EGF, and integrin ligation. PAK4 phosphorylates key substrates including LIMK1, cofilin, ??-catenin, and Bad, regulating cytoskeletal dynamics, cell migration, proliferation, and survival. It also phosphorylates transcription factors CREB and Smad2/3 and drives Wnt/??-catenin-mediated transcription of cyclin D1 and c-Myc. The kinase cross-talks with MAPK/ERK and PI3K/AKT pathways and interacts with scaffold proteins PIX, GIT1, and ILK to localize signaling.

In Raji cells, PAK4 knockout provides a physiologically relevant system to examine its roles in B-cell lymphomagenesis and therapy resistance. Disruption of PAK4 in this EBV-immortalized background allows dissection of its contributions to B-cell receptor downstream cascades, NF-??B activation, and survival programs. The model also facilitates study of integrin-mediated adhesion and migration pathways that influence lymphoma dissemination.

Applications include Western blot detection of phosphorylated LIMK1, ERK, and ??-catenin; proliferation assays (MTS, EdU); Transwell migration/invasion; apoptosis assays (annexin V); cytoskeletal staining; TCF/LEF reporter assays; and RT-qPCR of target genes. This polyclonal knockout product is also amenable to functional genomics screening and drug-resistance profiling. For additional information or to discuss your project, please contact Ascent Research.

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