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fasn  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc fasn
    Fasn, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 841 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fasn/Fatty+Acid+Synthase+Rabbit+mAb/pm42882471-83-41-42
    Average 96 stars, based on 841 article reviews
    fasn - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    SDS Page:

    Article Title: Impaired hepatic BMAL1-FGF21 signaling drives adverse metabolic outcomes of ketogenic diet.
    Article Snippet: Aims The ketogenic diet (KD) has gained popularity for its metabolic benefits; however, its effects vary markedly across physiological and pathological conditions.. This study aimed to determine the mechanisms underlying differential metabolic responses to KD.. Materials and Methods Db/db, liver-specific fibroblast growth factor 21 (FGF21) knockdown mice, and liverspecific brain and muscle aryl hydrocarbon receptor nuclear translocator-like 1 (BMAL1) knockout mice were treated with isocaloric KD for 8 weeks.

    Article Title: FASN-mediated metabolic reprogramming drives CD4 + T cell hyperactivation in Sjögren’s syndrome via fatty acid oxidation-dependent oxidative phosphorylation
    Article Snippet: Then protein extraction was carried out with RIPA lysis buffer (Beyotime, Shanghai, China). .. After SDS-PAGE separation and PVDF membrane transfer, the membrane was briefly sealed and detected overnight at 4 °C with primary antibodies targeting cell cycle regulators, including CDK2 (2546, CST, USA) and CDK4 (12790, CST, USA), oxidative phosphorylation related proteins, including COXIV (ab16056, Abcam, UK), ATP5A (ab176569, Abcam, UK), NDUFB8 (ab192878, Abcam, UK), FASN (3180, CST, USA) and β-Tublin (HRP-66240, Proteintech, China) (all diluted 1:1000). ..

    Membrane:

    Article Title: Impaired hepatic BMAL1-FGF21 signaling drives adverse metabolic outcomes of ketogenic diet.
    Article Snippet: Aims The ketogenic diet (KD) has gained popularity for its metabolic benefits; however, its effects vary markedly across physiological and pathological conditions.. This study aimed to determine the mechanisms underlying differential metabolic responses to KD.. Materials and Methods Db/db, liver-specific fibroblast growth factor 21 (FGF21) knockdown mice, and liverspecific brain and muscle aryl hydrocarbon receptor nuclear translocator-like 1 (BMAL1) knockout mice were treated with isocaloric KD for 8 weeks.

    Article Title: Citrulline Modulates Milk Fat Metabolism via the RTN3-FABP5 Axis in Bovine Mammary Epithelial Cells.
    Article Snippet: Milk fat critically determines the nutritional value, flavor, and processing characteristics of dairy products.. Citrulline, a nonproteinogenic amino acid enriched in cucurbitaceous fruits, has been implicated in lipid metabolism and metabolic health.. However, its function in milk fat synthesis within bovine mammary epithelial cells (BMECs) and the associated molecular mechanisms remain undefined.

    Article Title: FASN-mediated metabolic reprogramming drives CD4 + T cell hyperactivation in Sjögren’s syndrome via fatty acid oxidation-dependent oxidative phosphorylation
    Article Snippet: Then protein extraction was carried out with RIPA lysis buffer (Beyotime, Shanghai, China). .. After SDS-PAGE separation and PVDF membrane transfer, the membrane was briefly sealed and detected overnight at 4 °C with primary antibodies targeting cell cycle regulators, including CDK2 (2546, CST, USA) and CDK4 (12790, CST, USA), oxidative phosphorylation related proteins, including COXIV (ab16056, Abcam, UK), ATP5A (ab176569, Abcam, UK), NDUFB8 (ab192878, Abcam, UK), FASN (3180, CST, USA) and β-Tublin (HRP-66240, Proteintech, China) (all diluted 1:1000). ..

    Incubation:

    Article Title: Impaired hepatic BMAL1-FGF21 signaling drives adverse metabolic outcomes of ketogenic diet.
    Article Snippet: Aims The ketogenic diet (KD) has gained popularity for its metabolic benefits; however, its effects vary markedly across physiological and pathological conditions.. This study aimed to determine the mechanisms underlying differential metabolic responses to KD.. Materials and Methods Db/db, liver-specific fibroblast growth factor 21 (FGF21) knockdown mice, and liverspecific brain and muscle aryl hydrocarbon receptor nuclear translocator-like 1 (BMAL1) knockout mice were treated with isocaloric KD for 8 weeks.

    Article Title: LINC01357 reprograms fatty acid metabolism to facilitate the progression of triple-negative breast cancer by activating the MYH9-mediated Notch pathway
    Article Snippet: .. Membranes were incubated at 4 °C 215 overnight with the following primary antibodies: PCNA (60097-1-Ig, Proteintech, Wuhan, 216 China), E-cadherin (60335-1-Ig, Proteintech), N-cadherin (66219-1-Ig, Proteintech), 217 Vimentin (60330-1-Ig, Proteintech), HEY1 (19929-1-Ig, Proteintech), HES5 (22666-1-218 AP, Proteintech), Notch1 (10062-2-AP, Proteintech), ACC1 (21923-1-AP, Proteintech), 219 CD36 (18836-1-AP, Proteintech), CPT1A (15184-1-AP, Proteintech), MYH9 (11128-1-220 AP, Proteintech), α-Tubulin (66031-1-Ig, Proteintech), HES1 (A11718, Abclonal), Slug 221 (WL01508, Wanleibio, Shenyang, China), FASN (3180S, CST, Danvers, Massachusetts, 222 USA), Ki-67 (ab16667, Abcam, Cambridge, UK), and GAPDH (AP0063, Bioworld, 223 Nanjing, China). ..

    Phospho-proteomics:

    Article Title: FASN-mediated metabolic reprogramming drives CD4 + T cell hyperactivation in Sjögren’s syndrome via fatty acid oxidation-dependent oxidative phosphorylation
    Article Snippet: Then protein extraction was carried out with RIPA lysis buffer (Beyotime, Shanghai, China). .. After SDS-PAGE separation and PVDF membrane transfer, the membrane was briefly sealed and detected overnight at 4 °C with primary antibodies targeting cell cycle regulators, including CDK2 (2546, CST, USA) and CDK4 (12790, CST, USA), oxidative phosphorylation related proteins, including COXIV (ab16056, Abcam, UK), ATP5A (ab176569, Abcam, UK), NDUFB8 (ab192878, Abcam, UK), FASN (3180, CST, USA) and β-Tublin (HRP-66240, Proteintech, China) (all diluted 1:1000). ..

    Cell-Signaling:

    Article Title: Distinct OA:PA Ratios Generate Discrete Hepatocellular Phenotypes in HepG2 Cells.
    Article Snippet: Proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), transferred to polyvinylidene difluoride (PVDF) membranes (Bio-Rad, Hercules, CA, USA), blocked with 5% skim milk for 1 h, and incubated with primary antibodies overnight at 4 ◦C. .. Primary antibodies (all 1: 1000): AMPKα [Cell Signaling Technology (CST, Danvers, MA, USA) #2532], BAX (CST, Cat. No. 5023), BCL-2 (CST, Cat. No. 15071), BiP (CST, Cat. No. 3177S), CHOP (CST, Cat. No. 2895S), COX-2 (Abcam, Cambridge, UK, Cat. No. ab283574), FASN (CST, Cat. No. 3180S), FoxO3a (CST, Cat. No. 2497S), IL-1β (CST, https://doi.org/10.3390/cells15191774 Cat. No. 12242S), LC3A/B (CST, Cat. No. 4108S), mTOR (CST, Cat. No. 2983), NF-κB p65 (Abcam, Cat. No. ab32536), p62/SQSTM1 (CST, Cat. No. 5114S), phospho-AMPKα Thr172 (CST, Cat. No. 2535), phospho-FoxO3a Ser253 (CST, Cat. No. 9466S), phospho-mTOR Ser2448 (CST, Cat. No. 2971), phospho-NF-κB p65 Ser536 (CST, Cat. No. 3033S), SREBP-1 (CST, Cat. No. 95879S), and TNF-α (CST, Cat. No. 3707S). .. GAPDH–horseradish peroxidase (HRP) (ServiceBio, Wuhan, China, Cat. No. ZB15004-HRP; 1:5000) served as loading control for the main figure panels; recombinant anti-β-actin–HRP (ServiceBio, Cat. No. ZB15001HRP; 1:5000) served as loading control for the BAX/BCL-2 blots (Supplementary Figure S1).



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    Pathway enrichment analysis of the 25-gene signature. (A) Reactome enrichment analysis identified significant pathways, including fatty acid metabolism, cholesterol biosynthesis, and nuclear receptor signaling. (B) WikiPathways analysis corroborated the involvement of these genes in lipid metabolism pathways, including SREBF and MIR33 (microRNA 33) in cholesterol and lipid homeostasis. (C) Gene–pathway interaction network highlighting the central roles of lipid metabolism regulators fatty acid (FA) synthase ( <t>FASN</t> ) and stearoyl-coenzyme A (CoA) desaturase <t>(</t> <t>SCD</t> ) and other genes involved in the cell cycle and membrane trafficking, including TPD52 like 1 ( TPD52L1 ), leucine-rich repeats and immunoglobulin-like domains 1 ( LRIG1 ), keratin 7 ( KRT7 ), homeobox C4 ( HOXC4 ), and CDC42 effector protein 3 ( CDC42EP3 ).
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    Image Search Results


    Journal: iScience

    Article Title: A pan-tissue multi-omics resource atlas of coordinated immune, metabolic, and fibrotic alterations in diet-induced MASH

    doi: 10.1016/j.isci.2026.117139

    Figure Lengend Snippet:

    Article Snippet: Fatty Acid Synthase (FASN) Rabbit mAb , ABclonal , Cat# A19050; RRID: AB_2100796.

    Techniques: Recombinant, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Activity Assay, Transcriptomics, Mass Spectrometry, Reverse Transcription Polymerase Chain Reaction, Software

    Pathway enrichment analysis of the 25-gene signature. (A) Reactome enrichment analysis identified significant pathways, including fatty acid metabolism, cholesterol biosynthesis, and nuclear receptor signaling. (B) WikiPathways analysis corroborated the involvement of these genes in lipid metabolism pathways, including SREBF and MIR33 (microRNA 33) in cholesterol and lipid homeostasis. (C) Gene–pathway interaction network highlighting the central roles of lipid metabolism regulators fatty acid (FA) synthase ( FASN ) and stearoyl-coenzyme A (CoA) desaturase ( SCD ) and other genes involved in the cell cycle and membrane trafficking, including TPD52 like 1 ( TPD52L1 ), leucine-rich repeats and immunoglobulin-like domains 1 ( LRIG1 ), keratin 7 ( KRT7 ), homeobox C4 ( HOXC4 ), and CDC42 effector protein 3 ( CDC42EP3 ).

    Journal: Computational and Structural Biotechnology Journal

    Article Title: Epigenomics-Guided Multi-Omics Integration Uncovers a Lipid-Metabolic Signature with Translational Utility in Bladder Cancer

    doi: 10.34133/csbj.0139

    Figure Lengend Snippet: Pathway enrichment analysis of the 25-gene signature. (A) Reactome enrichment analysis identified significant pathways, including fatty acid metabolism, cholesterol biosynthesis, and nuclear receptor signaling. (B) WikiPathways analysis corroborated the involvement of these genes in lipid metabolism pathways, including SREBF and MIR33 (microRNA 33) in cholesterol and lipid homeostasis. (C) Gene–pathway interaction network highlighting the central roles of lipid metabolism regulators fatty acid (FA) synthase ( FASN ) and stearoyl-coenzyme A (CoA) desaturase ( SCD ) and other genes involved in the cell cycle and membrane trafficking, including TPD52 like 1 ( TPD52L1 ), leucine-rich repeats and immunoglobulin-like domains 1 ( LRIG1 ), keratin 7 ( KRT7 ), homeobox C4 ( HOXC4 ), and CDC42 effector protein 3 ( CDC42EP3 ).

    Article Snippet: In summary, 5,637 cells (1,000 cells per well) and J82 cells (500 cells per well) were seeded into 6-well plates and incubated at 37 °C for 24 h. The following day, one group served as the control and was maintained in the growth medium, while the experimental group received an addition of 50 μM FASN inhibitor (MedChemExpress, TVB-3664, catalog no. HY-120062) and SCD inhibitor (MedChemExpress, A939572, catalog no. HY-50709) to the growth medium and was cultured for a duration of 13 d. Subsequently, the cells were fixed with 4% formaldehyde (Sigma-Aldrich) and stained with 0.5% crystal violet (Sigma-Aldrich).

    Techniques: Membrane

    Prognostic validation and functional assessment of lipid metabolism regulators, fatty acid synthase ( FASN ) and stearoyl-coenzyme A desaturase ( SCD ). (A) Kaplan–Meier survival analysis indicating the prognostic significance of high expression levels of FASN (hazard ratio [HR] = 1.41) and SCD (HR = 1.8) in patients with bladder cancer (BLCA). (B) Expression analysis across stages revealed no significant variation (ANOVA, P = 0.3). (C) Colony formation assays demonstrating significantly reduced proliferation in BLCA cell lines (J82 and 5637) treated with the FASN inhibitor (FASNi; TVB-3664) and SCD inhibitor (SCDi; A939572). (D) Migration assays confirmed significantly impaired motility upon FASN and SCD inhibition, underscoring their roles in tumor aggressiveness. * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Journal: Computational and Structural Biotechnology Journal

    Article Title: Epigenomics-Guided Multi-Omics Integration Uncovers a Lipid-Metabolic Signature with Translational Utility in Bladder Cancer

    doi: 10.34133/csbj.0139

    Figure Lengend Snippet: Prognostic validation and functional assessment of lipid metabolism regulators, fatty acid synthase ( FASN ) and stearoyl-coenzyme A desaturase ( SCD ). (A) Kaplan–Meier survival analysis indicating the prognostic significance of high expression levels of FASN (hazard ratio [HR] = 1.41) and SCD (HR = 1.8) in patients with bladder cancer (BLCA). (B) Expression analysis across stages revealed no significant variation (ANOVA, P = 0.3). (C) Colony formation assays demonstrating significantly reduced proliferation in BLCA cell lines (J82 and 5637) treated with the FASN inhibitor (FASNi; TVB-3664) and SCD inhibitor (SCDi; A939572). (D) Migration assays confirmed significantly impaired motility upon FASN and SCD inhibition, underscoring their roles in tumor aggressiveness. * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Article Snippet: In summary, 5,637 cells (1,000 cells per well) and J82 cells (500 cells per well) were seeded into 6-well plates and incubated at 37 °C for 24 h. The following day, one group served as the control and was maintained in the growth medium, while the experimental group received an addition of 50 μM FASN inhibitor (MedChemExpress, TVB-3664, catalog no. HY-120062) and SCD inhibitor (MedChemExpress, A939572, catalog no. HY-50709) to the growth medium and was cultured for a duration of 13 d. Subsequently, the cells were fixed with 4% formaldehyde (Sigma-Aldrich) and stained with 0.5% crystal violet (Sigma-Aldrich).

    Techniques: Biomarker Discovery, Functional Assay, Expressing, Migration, Inhibition