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  • mProX™ Human CDC42BPB Stable Cell Line

    [CAT#: S01YF-1023-PY12]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase Cell Lines

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    Host Cell Type:
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    Based on this stable cell line, we also provide cell-based in vitro assays to evaluate the effects of your compounds or antibodies.

    Sub Cat Product Name Target Protein Species Host Cell Type Assay Types Inquiry Datasheet
    S01YF-1122-KX1229 Magic™ Human MRCKβ(CDC42BPB) in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;BT-549
    Target Classification
    Kinase Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Chilton-Okur-Chung Neurodevelopmental Syndrome; Myotonic Dystrophy
    Gene ID
    Human:9578
    UniProt ID
    Human:Q9Y5S2

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    CDC42BPB (Cell Division Cycle 42 Binding Protein Beta) has been implicated in various biological processes and diseases. One case report discusses the presence of potentially harmful variants in the CDC42BPB gene in a patient with Cardiofaciocutaneous Syndrome (CFCS), expanding our understanding of the symptom spectrum of the disease. Additionally, a study demonstrates that the inhibition of CDC42/MRCK signaling pathways by the Zhuidu Formula (ZDF) can suppress the migratory and invasive properties of triple-negative breast cancer cells. Another study identifies CDC42BPB as a candidate modifier gene for the penetrance of Leber's Hereditary Optic Neuropathy (LHON), suggesting its potential role in influencing the development of this disease. Finally, a study examining the effects of Cdc42bpb deletion in mice shows that heterozygous deletion of the gene does not significantly alter ethanol-related behaviors, but it is associated with mild hyperactivity and urogenital deformities in mice. Overall, CDC42BPB has been implicated in cellular migration, cancer metastasis, disease penetrance, and normal mouse behavior.

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    FAQ

    chat Jordan Davis (Verified Customer)

    What disorders are associated with CDC42BPB gene variants? May 19 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Variants in the CDC42BPB gene, which encodes MRCKβ, have been linked to neurodevelopmental disorders including developmental delay, intellectual disability, autism, and certain structural brain abnormalities. May 19 2022

    chat Taylor Davis (Verified Customer)

    How do mutations in CDC42BPB affect its function? Jul 29 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Mutations in CDC42BPB, including missense, frameshift, and nonsense variants, can disrupt the gene's function, potentially leading to haploinsufficiency and contributing to neurodevelopmental disorders. Jul 29 2021

    Published Data

    Fig.1 Inhibition of cell proliferation was achieved through the knockdown of CDC42BPA and CDC42BPB.

    In BT549 cells, knockdown of CDC42BPA and CDC42BPB was carried out, followed by a 5-day culture period and subsequent staining with crystal violet. The graph displays the relative cell density, based on data from three independent experiments.

    Ref: Yamaguchi, Hirohito, et al. "MRCK as a Potential Target for Claudin-Low Subtype of Breast Cancer." Int. J. Biol. Sci 1 (2024): 1.

    Pubmed: NA

    DOI: 10.7150/ijbs.88285

    Research Highlights

    Tang, Qiong. et al. "A Case Report of Cardiofaciocutaneous Syndrome with MAP2K1 Pathogenic Variant." Pharmacogenomics and personalized medicine, 2023.
    Cardiofaciocutaneous syndrome (CFCS) is an extremely rare disorder characterized by craniofacial dysmorphism, cardiac abnormalities, ectodermal abnormalities, psychomotor delay, intellectual disability, and short stature. Despite its rarity, about 300 cases have been reported in the literature. This study presents a case of CFCS in a patient who lacked the typical heart malformations but displayed craniofacial features, skin abnormalities, intellectual disability, and short stature. Genetic testing identified three potentially harmful variants, including a variant in the BRAF gene and two in the MAP2K1 gene. Further research is needed to understand the underlying mechanisms and to develop targeted treatments for CFCS.
    Tang, Qiong. et al. "A Case Report of Cardiofaciocutaneous Syndrome with MAP2K1 Pathogenic Variant." Pharmacogenomics and personalized medicine, 2023.
    Pubmed: 37705935   DOI: 10.2147/PGPM.S411964

    Wu, Qinhang. et al. "Zhuidu Formula suppresses the migratory and invasive properties of triple-negative breast cancer cells via dual signaling pathways of RhoA/ROCK and CDC42/MRCK." Journal of ethnopharmacology, 2023.
    The Zhuidu Formula (ZDF) is a combination of three active ingredients found in Tripterygium wilfordii Hook. F, dried toad skin, and Taxus wallichiana var. chinensis (Pilg) Florin, namely triptolide, cinobufagin, and paclitaxel. Modern studies have displayed these natural compounds' ability to hinder DNA synthesis, trigger apoptosis in tumor cells, and disrupt the tubulin balance, making them effective against tumor growth. Despite this, the mechanism through which they inhibit metastasis in triple-negative breast cancer (TNBC) remains unclear.
    Wu, Qinhang. et al. "Zhuidu Formula suppresses the migratory and invasive properties of triple-negative breast cancer cells via dual signaling pathways of RhoA/ROCK and CDC42/MRCK." Journal of ethnopharmacology, 2023.
    Pubmed: 37196814   DOI: 10.1016/j.jep.2023.116644

    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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