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Cat. No. ARG1456

EXOC6 Knockout Raji Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Bone

  • Disease:

    Burkitt lymphoma

The EXOC6 Knockout Raji Polyclonal Cells provide a CRISPR/Cas9-edited polyclonal knockout population from Burkitt lymphoma Raji B lymphocytes, disrupting EXOC6/Sec15 within the exocyst complex. This targeting impairs vesicle tethering, regulated by RalA/B and Arf6 GTPases, which is critical for cytokine secretion and membrane protein trafficking. This model allows investigation of exocytosis-dependent B cell functions including activation, immune synapse formation, and adhesion, with implications for lymphoma progression. Key applications encompass ELISA, flow cytometry, co-immunoprecipitation, and cellular activation assays, facilitating detailed mechanistic studies in immunology and oncology.

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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

    EXOC6

    Gene Identifier

    NCBI Gene ID 54536

    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% 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 EXOC6 Knockout Raji Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout cell population derived from the human Raji B lymphocyte line. This model employs CRISPR/Cas9-mediated gene disruption to generate a heterogeneous pool of EXOC6-deficient cells, serving as a loss-of-function tool for studying the exocyst complex in immune cell biology.

The Raji cell line is a lymphoblastoid B cell model isolated from a Burkitt lymphoma patient, characterized by EBV transformation and a hallmark MYC/IGH translocation. These suspension cells produce immunoglobulins and are widely employed to investigate B cell signaling, lymphoma pathogenesis, and therapeutic interventions due to their robust growth and well-characterized molecular features.

EXOC6 encodes Sec15, a core subunit of the exocyst complex responsible for tethering post-Golgi secretory vesicles to the plasma membrane. Its activity is governed by upstream regulators including RalA, RalB, and Arf6 GTPases, acting downstream of PI3K and growth factor receptors. Sec15 directly associates with exocyst partners SEC5, SEC3, SEC8, EXO70, and EXO84, and coordinates with vesicle SNARE proteins and actin regulators to facilitate polarized exocytosis. This machinery is essential for targeted secretion of cytokines and surface receptor delivery, processes critical for B cell activation and immune synapse formation.

In the Raji B cell context, EXOC6 knockout disrupts exocyst-dependent trafficking, impairing cytokine release and membrane protein localization. This provides a physiologically relevant system to dissect how defective secretion alters B cell receptor signaling, adhesion, and intercellular communication, and how such dysfunctions contribute to lymphoma progression and immune evasion.

Researchers can leverage this polyclonal population in a variety of assays: RT-qPCR and Western blotting for knockout confirmation, ELISA to quantify secreted cytokines, immunofluorescence and flow cytometry to analyze surface marker expression, co-immunoprecipitation to assess exocyst complex assembly, and B cell activation assays to evaluate functional outcomes. This product is a versatile platform for investigations into exocyst-mediated secretion in lymphocytes and for exploring trafficking-related mechanisms in cancer. For more information, please contact Ascent Research.

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