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  • mProX™ Human PRKCD Stable Cell Line

    [CAT#: S01YF-1023-PY64]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase Cell Lines

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    Host Cell Type:
    Membrane Protein Engineering:
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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-1222-KX444 Magic™ Human PKCδ(PRKCD) in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;A2780
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Autoimmune Research
    Related Diseases
    Autoimmune Lymphoproliferative Syndrome, Type Iii; Systemic Lupus Erythematosus 16
    Gene ID
    Human:5580
    UniProt ID
    Human:Q05655

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    PRKCD, also known as protein kinase C delta, has various applications in different fields. In the field of cancer research, a study found that TRIM69, a protein, can suppress the resistance to cell death (anoikis) and metastasis in gastric cancer cells by promoting the degradation of PRKCD through a process called ubiquitin-proteasome-mediated degradation. This suggests that targeting PRKCD could be a potential therapeutic approach for metastatic gastric cancer. Additionally, PRKCD has been implicated in the antioxidant and anti-inflammatory properties of lipophilic extracts from Polyscias fruticosa leaves and Liriope platyphylla seeds. These extracts contain compounds that regulate PRKCD and other target genes involved in oxidative stress and inflammation-related pathways. The antioxidant and anti-inflammatory effects of these extracts make them promising candidates for the development of functional foods and nutraceuticals. Furthermore, PRKCD deficiency has been linked to systemic lupus erythematosus and other autoimmune and immunodeficiency disorders. Understanding the role of PRKCD in immune tolerance and effector functions against pathogens is crucial for the diagnosis and management of these conditions. Overall, PRKCD has diverse applications in cancer research, natural product development, and immunology.

    Protocols

    Please visit our protocols page.

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    There are currently no Customer reviews or questions for mProX™ Human PRKCD Stable Cell Line (S01YF-1023-PY64). Click the button above to contact us or submit your feedback about this product.

    FAQ

    chat Cameron Smith (Verified Customer)

    How does PRKCD regulate basal mitophagy? Apr 22 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    PRKCD localizes to mitochondria and regulates the recruitment of ULK1-ATG13 during the induction of mitophagy. Apr 22 2023

    chat Skyler Smith (Verified Customer)

    What is the role of PRKCD in chronic obstructive pulmonary disease? Oct 17 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    PRKCD might be a potential therapeutic target for COPD by promoting inflammatory response, apoptosis, mitochondrial dysfunction, and MUC5AC hypersecretion. Oct 17 2020

    Published Data

    Fig.1 The proliferation of A2780 cells was assessed using the CCK-8 assay.

    Following PRKCD knockdown, a notable inhibition of A2780 proliferation was observed when compared to the control group.

    Ref: Yao, Lijuan, et al. "MiR181c inhibits ovarian cancer metastasis and progression by targeting PRKCD expression." International journal of clinical and experimental medicine 8.9 (2015): 15198.

    Pubmed: 26629004

    DOI: NA

    Research Highlights

    Sun, Linqing. et al. "TRIM69 suppressed the anoikis resistance and metastasis of gastric cancer through ubiquitin,Äíproteasome-mediated degradation of PRKCD." Oncogene, 2023.
    The tripartite motif (TRIM) protein family has been extensively studied in various human cancers, including gastric cancer (GC). However, the specific role of TRIM69 in the resistance to anoikis and metastasis of GC cells has yet to be determined. Through RNA-sequencing analysis, differentially expressed genes were identified in anoikis-resistant GC cells. The interaction between TRIM69 and PRKCD was further investigated through coimmunoprecipitation and mass spectrometry. The results revealed that TRIM69 was significantly downregulated in anoikis-resistant GC cells. Overexpression of TRIM69 effectively suppressed anoikis resistance and metastasis of GC cells in both in vitro and in vivo experiments, while silencing TRIM69 had the opposite effects. Mechanistically, TRIM69 was found to interact with PRKCD via its B-box domain and induce K48-linked polyubiquitination of PRKCD. Furthermore, TRIM69 also inhibited the production of BDNF in a PRKCD-dependent manner. Of note, the overexpression of PRKCD or BDNF counteracted the effects of TRIM69 on anoikis resistance and metastasis of GC cells. Interestingly, a TRIM69 mutant lacking ubiquitin E3 ligase activity failed to inhibit BDNF production.
    Sun, Linqing. et al. "TRIM69 suppressed the anoikis resistance and metastasis of gastric cancer through ubiquitin,Äíproteasome-mediated degradation of PRKCD." Oncogene, 2023.
    Pubmed: 37864033   DOI: 10.1038/s41388-023-02873-6

    H G Rarison, Razanamanana. et al. "Antioxidant and Anti-Inflammatory Mechanisms of Lipophilic Fractions from Polyscias fruticosa Leaves Based on Network Pharmacology, In Silico, and In Vitro Approaches." Foods (Basel, Switzerland), 2023.
    This research paper examines the relationship between social media usage and academic performance among college students. Data was gathered through surveys and interviews, revealing a negative impact of social media on students' academic performance. The study suggests that promoting awareness among students about managing their social media usage and implementing limits can help mitigate the distracting effects on academic responsibilities.
    H G Rarison, Razanamanana. et al. "Antioxidant and Anti-Inflammatory Mechanisms of Lipophilic Fractions from Polyscias fruticosa Leaves Based on Network Pharmacology, In Silico, and In Vitro Approaches." Foods (Basel, Switzerland), 2023.
    Pubmed: 37835296   DOI: 10.3390/foods12193643

    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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