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  • mProX™ Human SLAMF7 Stable Cell Line

    [CAT#: S01YF-1023-PY289]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:

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    Membrane Protein Engineering:
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    Product Information

    Target Family
    Other Targets
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;RAW264.7
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    Cancer Research
    Related Diseases
    Plasmablastic Lymphoma; Smoldering Myeloma
    Gene ID
    Human:57823
    UniProt ID
    Human:Q9NQ25

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    SLAMF7, also known as CS1, is a protein that has been studied in various medical contexts. In IgG4-related disease (IgG4-RD), SLAMF7 is being evaluated as a potential target for treatment, along with other biologics and targeted agents. In plasmablastic lymphoma (PBL), SLAMF7 is being investigated as a diagnostic marker and a potential target for therapy. In silica particles-induced pulmonary inflammation, SLAMF7 is implicated in autophagy dysfunction and m6A modification. In multiple myeloma (MM), SLAMF7 is considered a promising immunotherapeutic target, and monoclonal antibodies targeting SLAMF7 have shown positive outcomes in clinical trials. Additionally, SLAMF7 has been identified as a biomarker associated with MM in liquid biopsy analysis. These studies highlight the diverse applications of SLAMF7 in different diseases and its potential as a therapeutic target.

    Protocols

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    FAQ

    chat Cameron Davis (Verified Customer)

    What is the significance of SLAMF7 in multiple myeloma? Jun 11 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    SLAMF7 is highly expressed on immunosuppressive T cells in multiple myeloma, suggesting that anti-SLAMF7 antibodies can boost anti-tumor immune responses in cancer patients. Jun 11 2021

    chat Alex Smith (Verified Customer)

    How does SLAMF7 expression influence macrophage activation in inflammation? Jan 31 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    SLAMF7 up-regulation on macrophages drives superactivation in inflammatory human diseases, indicating its role in both acute and chronic inflammatory conditions. Jan 31 2022

    Published Data

    Fig.1 Reduced levels of proinflammatory cytokines were observed in RAW-SLAMF7 cells.

    A construction was undertaken to generate RAW264.7 cells that were stably expressed with SLAMF7 (termed RAW-SLAMF7), along with a set of control RAW-vector cells. The examination of mRNA levels for Tnf, Il1b, and Il6 in RAW-SLAMF7 cells in comparison to RAW vector cells was conducted at three distinct time points: 0 hours, 6 hours, and 12 hours post-LPS stimulation.

    Ref: Wu, Yongjian, et al. "SLAMF7 regulates the inflammatory response in macrophages during polymicrobial sepsis." The Journal of Clinical Investigation 133.6 (2023).

    Pubmed: 36749634

    DOI: 10.1172/JCI150224

    Research Highlights

    Groh, M. et al. "IgG4-related disease: A proteiform pathology with frequent chest manifestations." Revue des maladies respiratoires, 2023.
    IgG4-related disease (IgG4-RD) was first identified in the early 2000s, but its diverse symptoms had been previously documented under various terms. These symptoms are characterized by the presence of oligoclonal plasma cells and fibrosis associated with IgG4.
    Groh, M. et al. "IgG4-related disease: A proteiform pathology with frequent chest manifestations." Revue des maladies respiratoires, 2023.
    Pubmed: 37858433   DOI: 10.1016/j.rmr.2023.10.001

    Lin, Hui; Yan, Hai. "Newest Advances in Diagnosis and Treatment of Plasmablastic Lymphoma --Review." Zhongguo shi yan xue ye xue za zhi, No publication year..
    Plasmablastic lymphoma (PL/PBL) is a rare and highly aggressive type of lymphoma with a poor prognosis. Strict diagnostic and therapeutic criteria for PBL are lacking. Along with traditional plasma cell markers, SLAMF7 may serve as a valuable supplement for PBL diagnosis. High-dose chemotherapy in combination with bortezomib or lenalidomide shows promise as a first-line treatment. For second-line therapy, emerging treatments such as immune checkpoint inhibitors, CAR-T cell therapy, and novel targeted agents have shown potential to improve survival rates for PBL patients. This review focuses on the diagnosis, differentiation, first-line treatment, and management of relapsed/refractory PBL to further advance understanding of this disease.
    Lin, Hui; Yan, Hai. "Newest Advances in Diagnosis and Treatment of Plasmablastic Lymphoma --Review." Zhongguo shi yan xue ye xue za zhi, No publication year..
    Pubmed: 37846723   DOI: 10.19746/j.cnki.issn.1009-2137.2023.05.055

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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