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  • mProX™ Human FCGR1A Stable Cell Line

    [CAT#: S01YF-1023-PY156]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Fc Receptor Cell Lines

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    Product Information

    Target Family
    Fc Receptor
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;SK-OV-3
    Target Classification
    Fc Receptor Cell Lines
    Target Research Area
    Infectious Research
    Related Diseases
    Peritonitis; Pharyngitis
    Gene ID
    Human:2209
    UniProt ID
    Human:P12314

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    FCGR1A, also known as Fc gamma receptor Ia, has been studied in various contexts. In the field of tuberculosis, FCGR1A gene expression has been found to differ significantly between individuals with latent TB infection (LTBI) and active TB (ATB), suggesting its potential as a biomarker for distinguishing between the two conditions. In rheumatoid arthritis, FCGR1A has been identified as a molecular imaging marker for characterizing synovitis, a key feature of the disease. FCGR1A has also been implicated in maintaining sperm fertilization capacity during semen cryopreservation in sheep. Additionally, in the context of hereditary angioedema (HAE), FCGR1A gene expression levels have been found to be associated with disease severity. Finally, in the field of neuroinflammation induced by lead exposure, FCGR1A has been studied in the context of microglia and astroglia activation. Overall, FCGR1A has shown potential in various applications, including as a biomarker, imaging marker, and regulator of cellular function in different disease contexts.

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    FAQ

    chat Peyton Miller (Verified Customer)

    What is the role of FCGR1A in Alzheimer's disease? Jun 25 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    FCGR1A, along with other immune pathway genes, has been identified to associate with Alzheimer's disease through deleterious protein-coding variants. Jun 25 2020

    chat Jordan Miller (Verified Customer)

    Can FCGR1A serve as a biomarker in cancer? Aug 10 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    FCGR1A has been identified as a potential biomarker and is correlated with immune infiltration in various cancer types. Aug 10 2020

    Published Data

    Fig.1 The promotion of ovarian cancer cell proliferation by FCGR1A was observed, with a notable impact on cellular growth rates.

    Quantification was performed on CCK8 assays conducted with shctrl and shFCGR1A SKOV3 cells, encompassing a total of three replications. The findings unveiled a noteworthy decline in the growth of ovarian cancer (OC) cells as a direct consequence of FCGR1A knockdown.

    Ref: Jiang, Hui, et al. "CRISPR/Cas9-based genome-wide screening for Metastasis ability identifies FCGR1A regulating the metastatic process of ovarian cancer by targeting LSP1." (2023).

    Pubmed: NA

    DOI: NA

    Research Highlights

    Mutua, Florence. et al. "Type I interferons and Mycobacterium tuberculosis whole cell lysate induce distinct transcriptional responses in M. tuberculosis infection." Tuberculosis (Edinburgh, Scotland), 2023.
    Type I interferon (IFN)-induced genes exhibit promise in distinguishing active tuberculosis (ATB) from latent TB infection (LTBI) and healthy controls (HC), tracking treatment progress, and identifying individuals at risk of progressing to active disease. Researchers investigated the distinct impacts of IFN-α, IFN-β, and Mycobacterium tuberculosis whole cell lysate (Mtb WCL) stimulation on specific IFN-stimulated genes in peripheral blood mononuclear cells from individuals with LTBI, ATB, and HC. IFN-α and IFN-β stimulation led to increased gene expression, whereas Mtb WCL stimulation mostly maintained baseline levels, except for IL-1A and IL-1B genes, which were downregulated. Differential expression of specific genes in response to these stimuli showed promise in distinguishing between LTBI and ATB, suggesting potential for further mechanistic exploration and host-directed therapeutic strategies.
    Mutua, Florence. et al. "Type I interferons and Mycobacterium tuberculosis whole cell lysate induce distinct transcriptional responses in M. tuberculosis infection." Tuberculosis (Edinburgh, Scotland), 2023.
    Pubmed: 37729851   DOI: 10.1016/j.tube.2023.102409

    F Theeuwes, Wessel. et al. "CD64 as novel molecular imaging marker for the characterization of synovitis in rheumatoid arthritis." Arthritis research & therapy, 2023.
    Rheumatoid arthritis (RA) is a common and severe form of joint disease observed globally. Its main feature is inflammation of the synovial membrane (synovitis), which is closely associated with joint damage. To determine the presence and severity of synovitis, magnetic resonance imaging and ultrasonography are commonly utilized. Nonetheless, these diagnostic methods do not provide information on the activation status of certain inflammatory cells, particularly macrophages, which express the Fc gamma receptor CD64 and are known to play a significant role in synovitis.
    F Theeuwes, Wessel. et al. "CD64 as novel molecular imaging marker for the characterization of synovitis in rheumatoid arthritis." Arthritis research & therapy, 2023.
    Pubmed: 37653557   DOI: 10.1186/s13075-023-03147-y

    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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