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  • mProX™ Human GDF15 Stable Cell Line

    [CAT#: S01YF-1023-PY272]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:

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    Product Information

    Target Family
    Other Targets
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;HeLa;HT-3
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    Cardiovascular Research
    Related Diseases
    Heart Disease; Colorectal Cancer
    Gene ID
    Human:9518
    UniProt ID
    Human:Q99988

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Growth differentiation factor 15 (GDF15) has various applications in different fields. In the context of systemic sclerosis (SSc), GDF15 is implicated as a biomarker and potential therapeutic target due to its involvement in the fibrotic process of SSc. In older men undergoing resistance training, soy milk ingestion along with resistance training resulted in significant changes in muscular-related biomarkers, including GDF15, indicating its role in muscle mass, strength, and power. In patients with osteoarthritis (OA), GDF15 is identified as one of the characteristic genes associated with apoptosis and OA development. Additionally, GDF15 is found to be elevated in patients with Helicobacter pylori (HP) infection, suggesting a correlation between GDF15 levels and subclinical atherosclerosis. In mesangial cells, GDF15 interference regulates proliferation, inflammation, and autophagy by inhibiting the PI3K/AKT/mTOR signaling pathway. Overall, GDF15 has potential applications in the diagnosis, treatment, and understanding of various diseases and conditions.

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    FAQ

    chat Alex Johnson (Verified Customer)

    Does GDF15 play a role in normal erythroid differentiation? Jun 18 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GDF15 is essential in normal erythropoiesis and in the ineffective erythroid differentiation of patients with refractory anaemia with ring-sideroblasts, suggesting its significant role in erythroid development. Jun 18 2021

    chat Taylor Miller (Verified Customer)

    Can GDF15 influence mitochondrial membrane potential and antioxidant gene expression? Jul 31 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GDF15 enhances mitochondrial membrane potential and upregulates antioxidant genes, potentially improving embryo viability and implantation potential in mouse blastocysts cultured under low oxygen tension. Jul 31 2023

    Published Data

    Fig.1 The inhibition of EMT-related gene expression in cervical cancer cells was observed upon the knockdown of GDF15.

    The inhibition of EMT-related gene expression in cervical cancer cells was achieved through the knockdown of GDF15. In HT-3 and Hela cells, transfection with sh-GDF15 or sh-NC led to the detection of GDF15 expression using western blot assays.

    Ref: Li, Li, et al. "GDF15 knockdown suppresses cervical cancer cell migration in vitro through the TGF-β/Smad2/3/Snail1 pathway." FEBS Open Bio 10.12 (2020): 2750-2760.

    Pubmed: 33098235

    DOI: 10.1002/2211-5463.13013

    Research Highlights

    Muruganandam, Maheswari. et al. "Biomarkers in the Pathogenesis, Diagnosis, and Treatment of Systemic Sclerosis." Journal of inflammation research, 2023.
    Systemic sclerosis (SSc) is a complex autoimmune disease with vascular damage, vasoinstability, and decreased perfusion, leading to inflammation and fibrosis of the skin and internal organs. Biomarkers are important indicators of the disease processes within an individual and their accurate and reproducible measurement is crucial. The field of biomarkers in SSc is extensive, with over 240 pathways and proteins being implicated in the disease's development. Anti-nuclear antibodies (ANA) are classical biomarkers, with well-defined clinical classifications and are present in more than 90% of SSc patients. Transforming growth factor-β (TGF-β) is a central biomarker in SSc's fibrotic process, along with other newly identified biomarkers such as tyrosine kinases, interferon-1 signaling, IL-6 signaling, endogenous thrombin, PPARs, lysophosphatidic acid receptors, and amino acid metabolites. Several other biomarkers, including STAT4, CD226, IRF5, IRAK1, CTGF, NLRP1, CD3ζ, and the NLR family, have been implicated in a subtype of SSc called SSc-ILD. Genetic factors, including HLDRB1 alleles, also play a significant role in SSc. The role of various interleukins and chemokines (CCL, CXC, and CX3CL1) have also been identified as potential biomarkers, along with adiponectin and maresin-1, which are reduced in SSc patients. To determine disease activity and response to therapy, there has been a recent trend of using biomarker panels with complex multifactor analysis, machine learning, and artificial intelligence. This review discusses the various biomarkers involved in the pathology of SSc, including molecules, pathways, and receptors.
    Muruganandam, Maheswari. et al. "Biomarkers in the Pathogenesis, Diagnosis, and Treatment of Systemic Sclerosis." Journal of inflammation research, 2023.
    Pubmed: 37868834   DOI: 10.2147/JIR.S379815

    Hooshmand-Moghadam, Babak. et al. "Effects of soy milk ingestion immediately after resistance training on muscular-related biomarkers in older men: a randomized controlled trial." Biology of sport, 2023.
    The study aimed to investigate the impact of soy milk consumption on changes in body composition, strength, power, and biomarkers related to muscle function over a 12-week period of resistance training in older men. A total of 30 healthy older men (average age of 65.63 ± 3.16 years and body mass of 62.63 ± 3.86 kg) were randomly assigned to two groups: one receiving soy milk alongside resistance training (SR group) and the other receiving a placebo alongside resistance training (PR group). The SR group consumed 240 ml of non-dairy vanilla-flavored soy milk after each training session and on non-training days. Results showed significant differences in muscle mass, upper limb body strength (UBS), lower limb aerobic power (LAP), activin A, and GDF15 between the two groups (P < 0.05). Both groups experienced a significant decrease in body mass, body fat %, activin A, GDF15, and TGFβ1, as well as an increase in muscle mass, UBS, lower limb body strength, upper limb aerobic power, LAP, BDNF, and irisin compared to baseline (P < 0.05). The findings suggest that the consumption of soy milk during resistance training in older men can improve lean mass, strength, and power, and modulate the levels of skeletal muscle regulatory markers.
    Hooshmand-Moghadam, Babak. et al. "Effects of soy milk ingestion immediately after resistance training on muscular-related biomarkers in older men: a randomized controlled trial." Biology of sport, 2023.
    Pubmed: 37867735   DOI: 10.5114/biolsport.2023.123894

    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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