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Cat. No. ARG1275

MS4A1 Knockout Raji Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Bone

  • Disease:

    Burkitt lymphoma

MS4A1 Knockout Raji Polyclonal Cells provide a CRISPR/Cas9-edited polyclonal knockout population of the human Raji B lymphoblastoid cell line, with targeted disruption of MS4A1, the gene encoding CD20. This loss-of-function model eliminates CD20 surface expression, which normally functions as a calcium channel and co-modulator of B-cell receptor (BCR) signaling through interactions with kinases such as Lyn and effectors including SYK and AKT. The polyclonal knockout cells retain the Raji background's mature B-cell phenotype and are ideal for investigating CD20-dependent signaling, B-cell lymphoma biology, and the mechanism of anti-CD20 therapeutics like rituximab. Research applications span flow cytometry, calcium flux assays, drug sensitivity testing, and target validation studies in oncology and immunology.

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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

    MS4A1

    Gene Identifier

    NCBI Gene ID 931

    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 MS4A1 Knockout Raji Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout population derived from the human Raji B lymphoblastoid cell line, with disruption of the MS4A1 gene encoding CD20. This polyclonal knockout model eliminates CD20 protein expression, generating a loss-of-function system that retains the heterogeneity of the parental line while enabling controlled studies of B-cell biology.

The Raji cell line, originating from a Burkitt lymphoma patient, is Epstein?CBarr virus-positive and expresses mature B-cell markers including CD19, CD20, and surface immunoglobulin. As a suspension cell line, it serves as a robust model for B-cell malignancies, immune signaling, and lymphomagenesis, and supports efficient CRISPR/Cas9 editing and downstream functional assays.

MS4A1 encodes CD20, a tetraspanin that acts as a calcium-permeable channel and co-modulates B-cell receptor (BCR) signaling. CD20 forms homo-oligomers and interacts with the BCR complex, MHC class II, CD40, and Src kinases like Lyn. Upon BCR stimulation, CD20 facilitates calcium influx, activating SYK, BTK, and PLC??2, which drive PI3K/AKT and NF-??B pathways. Transcriptional regulation by PAX5, EBF1, and IL-4 receptor signaling controls CD20 levels. Downstream targets include MAPK cascades, NFAT, and c-Myc, linking CD20 to proliferation, differentiation, and survival.

In Raji cells, CD20 contributes to oncogenic BCR signaling. Knockout of MS4A1 selectively abolishes CD20 expression without affecting other B-cell markers, enabling dissection of CD20-specific functions in calcium-dependent pathways. This model is relevant for B-cell non-Hodgkin lymphoma, chronic lymphocytic leukemia, and autoimmune diseases such as rheumatoid arthritis and multiple sclerosis, where anti-CD20 therapies are used.

Applications include flow cytometric assessment of CD20 loss, western blotting for Lyn and AKT, calcium flux assays, proliferation and apoptosis studies, and drug sensitivity testing with rituximab. The polyclonal population is suitable for co-immunoprecipitation of CD20 partners and screening for alternative therapeutics. For technical inquiries or ordering details, please contact Ascent Research.

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