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rabbit polyclonal anti lc3 i ii  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit polyclonal anti lc3 i ii
    Rabbit Polyclonal Anti Lc3 I Ii, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+lc3/pmc13052180-62-119-124
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal anti lc3 i ii - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    other:

    Article Title: Non-Pharmaceutical Interventions Based on Diet Restriction and Exercise Improve Morphology and Function of Fatty Pancreas in Male WBN/Kob-Lepr (Fa/Fa) Rats
    Article Snippet: The following primary antibodies were used: rabbit anti-IL-6 (Abcam (Cambridge, UK), 6672), rabbit anti-XBP1 (Abcam, 37152), rabbit anti-LC3 (Cell Signaling (Danvers, MA, USA), 12741), rabbit anti-(SSAT1 (Proteintech (Rosemont, IL, USA), 10708-1-AP), rabbit anti-Glut4 (Millipore (Burlington, MA, USA), 07-1404), rabbit anti-HK2 (Millipore, AB3279), rabbit anti-CS (Cell Signaling, 14309), rabbit anti-COX IV (Cell Signaling, 4850), phosphorylated AMPKα Thr172 (Cell Signaling, 2535), and rabbit anti-PGC1 (Santacruz (Santa Cruz, CA, USA), SC-13067).

    Article Title: Mechanosensory channels mediate ER Ca 2+ transients to trigger assembly of autophagosome initiation sites for degradation of ER subdomains.
    Article Snippet: Article Mechanosensory channels mediate ER Ca2+ transients to trigger assembly of autophagosome initiation sites for degradation of ER subdomains

    Western Blot:

    Article Title: iPSCNPC transplantation alleviates brain injury after intracerebral hemorrhage in mice by downregulating autophagy via AMPK/ mTOR signaling pathway.
    Article Snippet: .. Protein extracts from brain tissues and astrocytes were prepared according to experimental requirements, and Western blotting was conducted as previously reported.33 Primary antibodies included: rabbit anti-AMPK (1:1000, CST), rabbit anti-phospho-AMPK (1:1000, CST), rabbit anti-mTOR (1:1000, CST), rabbit anti-phospho-mTOR (1:1000, CST), mouse anti-P62 (1:1000, Abcam), rabbit anti-LC3 (1:1000, CST), mouse anti-GFAP (1:1000, Servicebio), mouse anti-VIM (1:1000, Servicebio), and mouse anti-GAPDH (1:1000, Servicebio). .. Signals were detected using an enhanced chemiluminescence substrate (ThermoFisher Scientific) and imaged with a Tanon imaging system (Shanghai, China).

    Article Title: Early mitophagy activation by Urolithin A prevents, but late activation does not reverse, age-related cognitive impairment.
    Article Snippet: The fluo- rescent dyes used were: CM-H2DCFDA (catalog number C6827, Thermo Fisher Scientific), TPE-MI ( Tetraphenylethene maleimide)(Catalog number: HY-143218 Med Chem Express). .. The primary antibodies used were: mouse anti-β-actin (1:1000, sc-47778, Santa Cruz Biotechnology, Inc.), rabbit anti-GAPDH (1:1000, sc-25778, Santa Cruz Biotechnology, Inc.), rabbit anti-GAPDH (1:1000, sc25778, Santa Cruz Biotechnology, Inc.), mouse anti-synaptophysin (1:1000, sc-17750, Santa Cruz Biotechnology, Inc.), mouse anti-PSD95 (1:500, sc-32290, Santa Cruz Biotechnology, Inc.), mouse antiGluA1(1:100, sc13152, Santa Cruz Biotechnology,Inc.)., mouse anti-Total OXPHOS Human WB Antibody Cocktail (1:1000, ab110411, Abcam, Inc.), rabbit anti-Opa1 (1:1000, mAb 80471, Cell Signaling Technologies), mouse anti-Mfn1 (1:1000. sc-166644, Santa Cruz Biotechnology, Inc), rabbit antiMfn2 (1:1000, mAb 11925, Cell Signaling Technologies), rabbit anti-pDrp1 (1:1000 mAb 6319; mb 4494, Cell Signaling Technolo-gies), mouse anti-Drp1 (1:1000, sc-271583, Santa Cruz Biotechnology, Inc), rabbit anti-FUNDC1 (1:1000, PA5-77785, Invitrogen), mouse anti-TBK1 (sc-52957, Santa Cruz Biotechnology, Inc) mouse anti-PINK1 (1:1000, sc-517353, Santa Cruz Biotechnology, Inc.), mouse anti-Parkin (1:1000, sc-32282, Santa Cruz Biotechnology, Inc), rabbit anti-Nrf2 (1:1000, sc722, Santa Cruz Biotechnology, Inc.), mouse anti-PGC-1α (1:1000, sc-517380, Santa Cruz Biotechnology, Inc.), rabbit anti-p62 (1:1000, mAb 8025, Cell Signaling Technologies), rabbit anti-OPTN (1:1000, mAb 58981, Cell Signaling Technologies), rabbit anti-LC3 (1:1000, mAb 3868, Cell Signaling Technologies), rabbit anti-BNIP/NIX (1:1000, mAb 12396, Cell Signaling Technologies), rabbit antiSesn2 (1:1000, mAb 8487, Cell Signaling Technologies), rabbit anti-human tau (1:1000, 2024-10-31, Dako), mouse anti-tau PHF-1 (phosphorylated at Ser396 and Ser394) was a gift by Dr. Peter Davies (Department of Pathology, Albert Einstein College of Medicine, NY, USA. ..

    Incubation:

    Article Title: Large increases in resistance training volume do not impair skeletal muscle hypertrophy or anabolic–catabolic molecular signalling in trained individuals
    Article Snippet: .. The membranes were incubated overnight at 4°C with the following antibodies at a dilution of 1:1000 in TBST with 5% bovine serum albumin (BSA): rabbit anti-MyHC (cat. no: 64038, Cell Signaling Technology); rabbit anti-polyubiquitin (cat. no: 3933, Cell Signaling Technology); rabbit 20S antibody cocktail (cat. no: PW8155, Enzo Life Sciences); rabbit anti-calpain-1 (cat. no: 2556, Cell Signaling Technology); rabbit anti-calpain-2 (cat. no: 70655, Cell Signaling Technology); rabbit anti-LC3 (cat. no: 2775, Cell Signaling Technology); rabbit anti-FOXO1 (cat. no: 9454, Cell Signaling Technology); rabbit anti-FOXO3 (cat. no: 24975, Cell Signaling Technology); rabbit anti-RPS6 (cat. no: 2217, Cell Signaling Technology); rabbit anti-4EBP1 (cat. no: 9644, Cell Signaling Technology); rabbit anti-phospho-4EBP1 (cat. no: 2855, Cell Signaling Technology); rabbit anti-p62 (cat. no: 5114, Cell Signaling Technology); mouse anti-SKIV2L2 (cat. no: sc-515828, Santa Cruz Technology); mouse anti-G3BP1 (cat. no: sc-365338, Santa Cruz Technology); rabbit anti-p70S6K (cat. no: 9234, Cell Signaling Technology); rabbit anti-phospho-p70S6K (cat. no: 2983, Cell Signaling Technology); rabbit anti-mTOR (cat. no: 5536, Cell Signaling Technology); rabbit anti-phospho-mTOR (cat. no: 2971, Cell Signaling Technology). ..



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    LIPUS promotes mitophagy in high glucose-stimulated HUVECs. ( A – D ) Representative protein bands and quantitative analysis of p62, <t>LC3-II,</t> and TOM20 protein levels; one-way ANOVA ( n = 3). ( E ) Immunofluorescence co-staining of LC3 (green), TOM20 (red), and DAPI (blue). The scale bar was set to 20 μm ( n = 3). ( F ) 3D surface plot of LC3 fluorescence. ( G ) Fluorescence intensity distribution profiles for LC3 and TOM20. Green represents LC3; red represents TOM20. ( H ) Quantification of LC3-TOM20 co-localization. Co-localization was quantified with the overlap coefficient calculated with ImageJ (Colocalization Finder plugin). A total of 16–21 cells per group were analyzed; one-way ANOVA ( n = 3); ns, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars represent SD of the mean.
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    Cell Signaling Technology Inc rabbit polyclonal anti lc3 i ii
    LIPUS promotes mitophagy in high glucose-stimulated HUVECs. ( A – D ) Representative protein bands and quantitative analysis of p62, <t>LC3-II,</t> and TOM20 protein levels; one-way ANOVA ( n = 3). ( E ) Immunofluorescence co-staining of LC3 (green), TOM20 (red), and DAPI (blue). The scale bar was set to 20 μm ( n = 3). ( F ) 3D surface plot of LC3 fluorescence. ( G ) Fluorescence intensity distribution profiles for LC3 and TOM20. Green represents LC3; red represents TOM20. ( H ) Quantification of LC3-TOM20 co-localization. Co-localization was quantified with the overlap coefficient calculated with ImageJ (Colocalization Finder plugin). A total of 16–21 cells per group were analyzed; one-way ANOVA ( n = 3); ns, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars represent SD of the mean.
    Rabbit Polyclonal Anti Lc3 I Ii, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc rabbit anti lc3
    LIPUS promotes mitophagy in high glucose-stimulated HUVECs. ( A – D ) Representative protein bands and quantitative analysis of p62, <t>LC3-II,</t> and TOM20 protein levels; one-way ANOVA ( n = 3). ( E ) Immunofluorescence co-staining of LC3 (green), TOM20 (red), and DAPI (blue). The scale bar was set to 20 μm ( n = 3). ( F ) 3D surface plot of LC3 fluorescence. ( G ) Fluorescence intensity distribution profiles for LC3 and TOM20. Green represents LC3; red represents TOM20. ( H ) Quantification of LC3-TOM20 co-localization. Co-localization was quantified with the overlap coefficient calculated with ImageJ (Colocalization Finder plugin). A total of 16–21 cells per group were analyzed; one-way ANOVA ( n = 3); ns, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars represent SD of the mean.
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    ANXA3 did not regulate myocardial free fatty acid uptake or lipolysis but positively modulated macroautophagy in T2DM mice. (A-C) Relative p62 protein expression level and <t>LC3</t> II/I ratio in heart tissues of db/m and db/db mice analyzed by Western blot, n = 4. (D-F) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of mice analyzed by Western blot, n = 4. (G-I) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6. (J-L) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6-8. The data were presented as the mean ± SD. ∗ P < 0.05 versus the db/m group or the db/db + OE-GFP group; ∗∗ P < 0.01 versus the db/m group or the vehicle group or the OE-NC + vehicle group; ∗∗∗ P < 0.001 versus the vehicle group or the OE-NC + vehicle group; # P < 0.05 versus the OE-NC + HGPA group; ### P < 0.001 versus the OE-NC + HGPA group.
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    Novus Biologicals rabbit anti lc3
    ANXA3 did not regulate myocardial free fatty acid uptake or lipolysis but positively modulated macroautophagy in T2DM mice. (A-C) Relative p62 protein expression level and <t>LC3</t> II/I ratio in heart tissues of db/m and db/db mice analyzed by Western blot, n = 4. (D-F) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of mice analyzed by Western blot, n = 4. (G-I) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6. (J-L) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6-8. The data were presented as the mean ± SD. ∗ P < 0.05 versus the db/m group or the db/db + OE-GFP group; ∗∗ P < 0.01 versus the db/m group or the vehicle group or the OE-NC + vehicle group; ∗∗∗ P < 0.001 versus the vehicle group or the OE-NC + vehicle group; # P < 0.05 versus the OE-NC + HGPA group; ### P < 0.001 versus the OE-NC + HGPA group.
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    ANXA3 did not regulate myocardial free fatty acid uptake or lipolysis but positively modulated macroautophagy in T2DM mice. (A-C) Relative p62 protein expression level and <t>LC3</t> II/I ratio in heart tissues of db/m and db/db mice analyzed by Western blot, n = 4. (D-F) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of mice analyzed by Western blot, n = 4. (G-I) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6. (J-L) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6-8. The data were presented as the mean ± SD. ∗ P < 0.05 versus the db/m group or the db/db + OE-GFP group; ∗∗ P < 0.01 versus the db/m group or the vehicle group or the OE-NC + vehicle group; ∗∗∗ P < 0.001 versus the vehicle group or the OE-NC + vehicle group; # P < 0.05 versus the OE-NC + HGPA group; ### P < 0.001 versus the OE-NC + HGPA group.
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    Image Search Results


    LIPUS promotes mitophagy in high glucose-stimulated HUVECs. ( A – D ) Representative protein bands and quantitative analysis of p62, LC3-II, and TOM20 protein levels; one-way ANOVA ( n = 3). ( E ) Immunofluorescence co-staining of LC3 (green), TOM20 (red), and DAPI (blue). The scale bar was set to 20 μm ( n = 3). ( F ) 3D surface plot of LC3 fluorescence. ( G ) Fluorescence intensity distribution profiles for LC3 and TOM20. Green represents LC3; red represents TOM20. ( H ) Quantification of LC3-TOM20 co-localization. Co-localization was quantified with the overlap coefficient calculated with ImageJ (Colocalization Finder plugin). A total of 16–21 cells per group were analyzed; one-way ANOVA ( n = 3); ns, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars represent SD of the mean.

    Journal: Metabolites

    Article Title: Regulation of Mitophagy by Low-Intensity Pulsed Ultrasound Attenuates Endothelial Dysfunction

    doi: 10.3390/metabo16050329

    Figure Lengend Snippet: LIPUS promotes mitophagy in high glucose-stimulated HUVECs. ( A – D ) Representative protein bands and quantitative analysis of p62, LC3-II, and TOM20 protein levels; one-way ANOVA ( n = 3). ( E ) Immunofluorescence co-staining of LC3 (green), TOM20 (red), and DAPI (blue). The scale bar was set to 20 μm ( n = 3). ( F ) 3D surface plot of LC3 fluorescence. ( G ) Fluorescence intensity distribution profiles for LC3 and TOM20. Green represents LC3; red represents TOM20. ( H ) Quantification of LC3-TOM20 co-localization. Co-localization was quantified with the overlap coefficient calculated with ImageJ (Colocalization Finder plugin). A total of 16–21 cells per group were analyzed; one-way ANOVA ( n = 3); ns, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars represent SD of the mean.

    Article Snippet: The primary antibody, Rabbit anti-LC3 antibody (1:200, Abmart, T55992 ) and mouse anti-TOM20 antibody (1:200, Proteintech, Wuhan, China, 666777-1-Ig), diluted in blocking solution, was applied overnight at 4 °C.

    Techniques: Immunofluorescence, Staining, Fluorescence

    ANXA3 did not regulate myocardial free fatty acid uptake or lipolysis but positively modulated macroautophagy in T2DM mice. (A-C) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of db/m and db/db mice analyzed by Western blot, n = 4. (D-F) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of mice analyzed by Western blot, n = 4. (G-I) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6. (J-L) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6-8. The data were presented as the mean ± SD. ∗ P < 0.05 versus the db/m group or the db/db + OE-GFP group; ∗∗ P < 0.01 versus the db/m group or the vehicle group or the OE-NC + vehicle group; ∗∗∗ P < 0.001 versus the vehicle group or the OE-NC + vehicle group; # P < 0.05 versus the OE-NC + HGPA group; ### P < 0.001 versus the OE-NC + HGPA group.

    Journal: Redox Biology

    Article Title: YY1 nitration participates in DbCM cardiomyocyte lipotoxicity by inhibiting ANXA3 -induced microlipophagy

    doi: 10.1016/j.redox.2026.104085

    Figure Lengend Snippet: ANXA3 did not regulate myocardial free fatty acid uptake or lipolysis but positively modulated macroautophagy in T2DM mice. (A-C) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of db/m and db/db mice analyzed by Western blot, n = 4. (D-F) Relative p62 protein expression level and LC3 II/I ratio in heart tissues of mice analyzed by Western blot, n = 4. (G-I) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6. (J-L) Relative p62 protein expression level and LC3 II/I ratio in AC16 cardiomyocytes analyzed by Western blot, n = 6-8. The data were presented as the mean ± SD. ∗ P < 0.05 versus the db/m group or the db/db + OE-GFP group; ∗∗ P < 0.01 versus the db/m group or the vehicle group or the OE-NC + vehicle group; ∗∗∗ P < 0.001 versus the vehicle group or the OE-NC + vehicle group; # P < 0.05 versus the OE-NC + HGPA group; ### P < 0.001 versus the OE-NC + HGPA group.

    Article Snippet: Blocked with 5% (w/v) non-fat-dried milkat room temperature for 1 h. Then the membranes were incubated with the anti-ANXA3 antibody (Proteintech, 11804-1-AP; 1:1000 [v/v]), the anti-YY1 antibody (Proteintech, 22156-1-AP; 1:1000 [v/v]) the anti-PLIN2 antibody (Proteintech, 15294-1-AP; 1:1000 [v/v]), the anti-SQSTM1/p62 antibody (Cell Signaling Technology, 23214; 1:1000 [v/v]), the anti-LC3 antibody (Cell Signaling Technology, 12741; 1:1000 [v/v]), the anti-Rab7 antibody (Proteintech, 55469-1-AP; 1:1000 [v/v])or the rabbit anti-α-Tubulin antibody (ABclonal, AC031; 1:1000 [v/v])overnight at 4 °C.

    Techniques: Expressing, Western Blot