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rabbit anti lc3a b  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti lc3a b
    Rabbit Anti Lc3a B, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 4879 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lc3a+b+antibody/LC3A%2FB+Antibody/pmc12885221-442-12-15
    Average 97 stars, based on 4879 article reviews
    rabbit anti lc3a b - by Bioz Stars, 2026-09
    97/100 stars

    Images

    Related Articles

    Blocking Assay:

    Article Title: Radiosensitizing effects of Withaferin A in gastric cancer cells via autophagy Inhibition and mitochondrial disruption.
    Article Snippet: .. After blocking, the membranes were incubated at 4 °C overnight with the following primary antibodies(1:1000): cleaved caspase-3 antibody (ab2302;Abcam, Cambridge, UK), caspase-3 antibody (ab32351;Abcam), cleaved PARP1 antibody (ab32561;Abcam); PARP1 antibody (ab32138;Abcam); LC3A/B antibody (4108 S, Cell Signaling Technology, MA, USA), SQSTM1/p62 antibody (8025,Cell Signaling Technology), β-actin (3700 S, Cell Signaling Technology) and then with HRPconjugated secondary antibodies (1:5000; Cell Signaling Technology) at room temperature for 1 h, followed by washing with TBST. ..

    Incubation:

    Article Title: Radiosensitizing effects of Withaferin A in gastric cancer cells via autophagy Inhibition and mitochondrial disruption.
    Article Snippet: .. After blocking, the membranes were incubated at 4 °C overnight with the following primary antibodies(1:1000): cleaved caspase-3 antibody (ab2302;Abcam, Cambridge, UK), caspase-3 antibody (ab32351;Abcam), cleaved PARP1 antibody (ab32561;Abcam); PARP1 antibody (ab32138;Abcam); LC3A/B antibody (4108 S, Cell Signaling Technology, MA, USA), SQSTM1/p62 antibody (8025,Cell Signaling Technology), β-actin (3700 S, Cell Signaling Technology) and then with HRPconjugated secondary antibodies (1:5000; Cell Signaling Technology) at room temperature for 1 h, followed by washing with TBST. ..

    Article Title: TFEB overexpression alleviates autophagy-lysosomal deficits caused by progranulin insufficiency
    Article Snippet: .. Fixed cells were blocked in 3% BSA (Fisher Scientific) and 0.5% saponin (MilliporeSigma) in PBS, then incubated overnight with an LC3A/B antibody (Cell Signaling Technologies #12741) in the same solution. .. The following day, coverslips were washed in PBS before incubation with an AlexaFluor 594 donkey anti-rabbit antibody (Thermo Fisher) before mounting onto slides with Prolong Gold reagent.

    FLAG-tag:

    Article Title: Transcription factor GATA5 enhances autophagy by modulating miR-2765 in Penaeus vannamei under ammonia nitrogen stress.
    Article Snippet: The transcription factor GATA is recognized as a key regulator of cell generation and differentiation, playing a significant regulatory role in immune responses triggered by both biotic and abiotic stress.. However, the regulatory network of GATA in crustaceans remains poorly understood.. In this study, we identified a GATA5-like protein, designated as PvGATA5, from Penaeus vannamei.



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    Cell Signaling Technology Inc anti lc3 antibody
    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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    Cell Signaling Technology Inc lc3a b
    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.
    Lc3a B, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc antibodies against lc3a b
    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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    Cell Signaling Technology Inc lc3ii
    ADAMTS13 exerted partial inhibitory effects on both autophagy and mitophagy in DN mice. (A) Representative images and quantification of Beclin-1 <t>and</t> <t>LC3II/I</t> by western blot analysis ( N = 3). (B, C) Representative renal immunohistochemical staining of PINK1 and PARK2/Parkin in the kidney and quantitative analysis. Scale bar: 30 μm ( N = 5). Results were presented as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, one-way ANOVA followed by Tukey’s post hoc test.
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    Cell Signaling Technology Inc rabbit anti lc3b antibody
    ADAMTS13 exerted partial inhibitory effects on both autophagy and mitophagy in DN mice. (A) Representative images and quantification of Beclin-1 <t>and</t> <t>LC3II/I</t> by western blot analysis ( N = 3). (B, C) Representative renal immunohistochemical staining of PINK1 and PARK2/Parkin in the kidney and quantitative analysis. Scale bar: 30 μm ( N = 5). Results were presented as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, one-way ANOVA followed by Tukey’s post hoc test.
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    Image Search Results


    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

    ADAMTS13 exerted partial inhibitory effects on both autophagy and mitophagy in DN mice. (A) Representative images and quantification of Beclin-1 and LC3II/I by western blot analysis ( N = 3). (B, C) Representative renal immunohistochemical staining of PINK1 and PARK2/Parkin in the kidney and quantitative analysis. Scale bar: 30 μm ( N = 5). Results were presented as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, one-way ANOVA followed by Tukey’s post hoc test.

    Journal: Renal Failure

    Article Title: ADAMTS13 ameliorates diabetic nephropathy by Nrf2/GPX4/eNOS signaling pathway

    doi: 10.1080/0886022X.2026.2646089

    Figure Lengend Snippet: ADAMTS13 exerted partial inhibitory effects on both autophagy and mitophagy in DN mice. (A) Representative images and quantification of Beclin-1 and LC3II/I by western blot analysis ( N = 3). (B, C) Representative renal immunohistochemical staining of PINK1 and PARK2/Parkin in the kidney and quantitative analysis. Scale bar: 30 μm ( N = 5). Results were presented as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, one-way ANOVA followed by Tukey’s post hoc test.

    Article Snippet: Equal amounts of protein were loaded on 8–12% sodium dodecyl sulfate-polyacrylamide gels, transferred to polyvinylidene fluoride membrane (PVDF) (Thermo Fisher Scientific, Waltham, MA), and blocked with 5% skim milk powder for 2 h. Membranes were incubated overnight at 4 °C with the following primary antibodies: Beclin-1 (A7353, ABclonal, Wuhan, China); LC3II/I (#4108, 14/16 kDa, CST, Danvers, MA); Nrf2 (ab31163, Abcam, Cambridge, UK); SOD1 (A12537, ABclonal, Wuhan, China); SOD2 (A21805, ABclonal, Wuhan, China); GPX4 (A1933, ABclonal, Wuhan, China); eNOS (#32027, CST, Danvers, MA); p-eNOS (Ser 1177) (AF5812, Beyotime, Shanghai, China); β-actin (AF5002, Beyotime, Shanghai, China); GAPDH (AC001, ABclonal, Wuhan, China); Histone H3 (A2348, ABclonal, Wuhan, China).

    Techniques: Western Blot, Immunohistochemical staining, Staining