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  • mProX™ Human MLNR Stable Cell Line

    [CAT#: S01YF-0923-PY123]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    MLNR
    Target Family
    Motilin Family
    Target Protein Species
    Human
    Host Cell Type
    MRC5-SV40;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Digestive and Renal Research;Metabolic Research
    Related Diseases
    Gastroparesis;Diabetic Autonomic Neuropathy
    Gene ID
    Human: 2862
    UniProt ID
    Human: O43193

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The Motilin Receptor (MLNR) is a G-protein-coupled receptor that plays a pivotal role in gastrointestinal motility and the regulation of interdigestive migrating contractions. Research has shown that MLNR is a target for motilin, a peptide hormone, which is crucial for stimulating gastric motility. The activation of MLNR by motilin leads to increased gastrointestinal motility, which is essential for the movement of food and waste through the digestive tract. In therapeutic applications, MLNR agonists have been explored as potential treatments for gastrointestinal motility disorders, such as gastroparesis.

    Protocols

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    FAQ

    chat William (Verified Customer)

    What is the prognostic value of MLNR in gastric cancer patients? Apr 08 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    MLNR, or metastatic lymph node ratio, is a significant predictor for the survival of patients with gastric cancer. It can provide insights into the extent of lymph node involvement and metastasis. Apr 08 2022

    chat Jessica (Verified Customer)

    How does MLNR relate to colon cancer prognosis? Aug 10 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    The combined detection of MLNR and serum CEA (carcinoembryonic antigen) can predict distant metastasis in stage II-III colon cancer patients after radical resection. Aug 10 2022

    Published Data

    Fig.1 The DNA damage-up phenotypes were validated by MLNR knockdown using two separate siRNAs.

    Knockdown experiments using two distinct siRNAs, targeting MLNR, MME, and POMC, successfully validated the induction of DNA damage-associated traits. The assessment of DNA damage was performed through either the median fluorescence intensity measurement or the identification of a DNA-damage positive subpopulation. Displayed below are representative dot plots from flow cytometry illustrating instances of the DNA-damage positive subpopulation.

    Ref: Liu, Yanhong, et al. "Rare deleterious germline variants and risk of lung cancer." NPJ precision oncology 5.1 (2021): 12.

    Pubmed: 33594163

    DOI: 10.1038/s41698-021-00146-7

    Research Highlights

    Caliskan Yildirim E, et al. "Treatment Outcomes and Prognostic Factors in N3 Stage Gastric Cancer After ." Cancer management and research, 2023.
    N3 gastric cancer is known for its high incidence of lymph node metastasis and unfavorable outcomes despite optimal treatment. To accurately predict the prognosis of patients who underwent curative surgery for N3 gastric cancer, a comprehensive evaluation tool is needed due to the limitations of TNM classification. This study examined the overall survival (OS) of 169 patients who underwent (sub)total gastrectomy and regional lymph node dissection between November 2005 and September 2018. Cox regression analysis revealed significant prognostic factors such as gender, patient performance status, metastatic lymph node ratio (MLNR), tumor grade, and adjuvant chemotherapy. The five-year OS rate was 15%, and most recurrences occurred as distant metastases. Poor prognostic factors included male gender, poor performance status, grade 3 tumors, MLNR> 0.37, and lack of adjuvant chemotherapy. Given the high recurrence rates, further research is necessary to improve treatment approaches for N3 gastric cancer.
    Pubmed: 37809035   DOI: 10.2147/CMAR.S412270

    He Z, et al. "Development and external validation of a nomogram predicting overall survival for ." Scandinavian journal of gastroenterology, 2023.
    The aim of the study was to develop and validate a nomogram for predicting the overall survival (OS) of patients with gastric adenocarcinoma who underwent radical gastrectomy. The training cohort consisted of 3492 patients from 2012 to 2017. Prognostic factors were identified through survival analysis and COX analysis. The nomogram included age, type of surgery, tumor size, T stage, grade, and metastatic lymph node ratio (MLNR). The nomogram outperformed the American Joint Committee on Cancer (AJCC) TNM staging in both the training and external validation cohorts. The nomogram also showed good agreement with actual survival rates and improved predictive ability for 1-year, 3-year, and 5-year OS. The study highlights the potential of using the MLNR-based nomogram to guide clinical treatment decisions and improve survival outcomes for patients with gastric adenocarcinoma.
    Pubmed: 37632275   DOI: 10.1080/00365521.2023.2250497

    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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