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rabbit anti β actin  (Proteintech)


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    Structured Review

    Proteintech rabbit anti β actin
    Rabbit Anti β Actin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 3306 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+%CE%B2+actin+rabbit+polyclonal/beta+Actin+Polyclonal+antibody/pm42822338-56-0-9
    Average 96 stars, based on 3306 article reviews
    rabbit anti β actin - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Sandwich ELISA:

    Article Title: Elucidation of the Immunotoxicity of PEDOT: PSS on RAW264.7 Macrophages by Oxidative Stress, Inflammatory Response, and NF-κB Pathway Activation
    Article Snippet: Poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS) nanoparticles, widely used conductive polymers, pose environmental and health risks due to their nanoscale dispersion.. However, the characteristics of PEDOT: PSS in aquatic systems and the underlying mechanisms of its toxicity in animal and cell models remain poorly understood.. This study aimed to investigate the toxicological effects of PEDOT: PSS nanoparticles on macrophages, with a focus on RAW 264.7 cells.

    Western Blot:

    Article Title: ZIKV envelope protein is a strong blocker of early directional differentiation in the neural lineage.
    Article Snippet: The protein bands were visualized using the enhanced chemiluminescent (ECL) system (Perkin Elmer) and then analyzed using ChemoStar 6.0 Imaging Software (INTAS). .. Primary antibodies used in Western blotting include anti-DYKDDDDK-Tag-Mouse-Monoclonal (1:2000, Proteintech, Cat No. 66008-4-Ig), anti-PAX6-Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 12323–1-AP), antiβ-III-Tubulin-Mouse-Monoclonal (1:2000, Abclonal, Cat No. A18132), anti-Cleaved Caspase3-Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 25128-1-AP), anti- Caspase 9/P35-Rabbit-Polyclonal (1:300, Proteintech, Cat No. 10380-1-AP), anti-Phospho-P53(Ser15)-Rabbit-Polyclonal (1:2000, Proteintech, Cat No. 28961-1-AP), anti-BaxMouse-Polyclonal (1:10000, Proteintech, Cat No. 60283-2-Ig), anti-Bcl2-Rabbit-Polyclonal (1:500, Proteintech, AR TI CL E IN P RE SS Cat No. 26593-1-AP), anti-NLRP3-Rabbit-Polyclonal (1:1000, abcam, Cat No. ab4207), anti-GSDMD-RabbitMonoclonal (1:1000, abcam, Cat No. ab209845), anti-Caspase1-Rabbit-Monoclonal (1:1000, abcam, Cat No. ab207802), anti-KLF2-Rabbit-Polyclonal (1:200, Signalway Antibody, Cat No. #46591), anti-DPPA2-RabbitPolyclonal (1:1000, Signalway Antibody, Cat No. #62249), anti-Calretinin-Rabbit-Polyclonal (1:500, EpiZyme, Cat No. #P011307), anti-p57 Kip2-Rabbit-Monoclonal (1:500, Zenbio, Cat No. #R380868), anti-L1TD1-RabbitPolyclonal (1:1000, Signalway Antibody, Cat No. #62248), anti-WNT7A-Rabbit-Polyclonal (1:1000, Signalway Antibody, Cat No. #38653-1), anti-GRIK2-Rabbit-Monoclonal (1:500, Zenbio, Cat No. #R389225), anti-ROBO2Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 21635-1-AP), anti-β-actin-Rabbit-Polyclonal (1:2000, Proteintech, Cat No: 20536-1-AP), anti-GAPDH-Mouse-Polyclonal (1:5000, EpiZyme, Cat No. LF205). .. The secondary antibodies include horseradish peroxidase (HRP)-conjugated Goat anti-Rabbit IgG (H + L) (1:2000, Abclonal, Cat No. A5014) or HRP-conjugated Goat anti-Mouse IgG (H + L) (1:5000, Proteintech, Cat No. SA0000-1-1).

    Article Title: ZIKV envelope protein is a strong blocker of early directional differentiation in the neural lineage
    Article Snippet: The protein bands were visualized using the enhanced chemiluminescent (ECL) system (Perkin Elmer) and then analyzed using ChemoStar 6.0 Imaging Software (INTAS). .. Primary antibodies used in Western blotting include anti-DYKDDDDK-Tag-Mouse-Monoclonal (1:2000, Proteintech, Cat No. 66008-4-Ig), anti-PAX6-Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 12323–1-AP), anti-β-III-Tubulin-Mouse-Monoclonal (1:2000, Abclonal, Cat No. A18132), anti-Cleaved Caspase3-Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 25128-1-AP), anti- Caspase 9/P35-Rabbit-Polyclonal (1:300, Proteintech, Cat No. 10380-1-AP), anti-Phospho-P53(Ser15)-Rabbit-Polyclonal (1:2000, Proteintech, Cat No. 28961-1-AP), anti-Bax-Mouse-Polyclonal (1:10000, Proteintech, Cat No. 60283-2-Ig), anti-Bcl2-Rabbit-Polyclonal (1:500, Proteintech, Cat No. 26593-1-AP), anti-NLRP3-Rabbit-Polyclonal (1:1000, abcam, Cat No. ab4207), anti-GSDMD-Rabbit-Monoclonal (1:1000, abcam, Cat No. ab209845), anti-Caspase1-Rabbit-Monoclonal (1:1000, abcam, Cat No. ab207802), anti-KLF2-Rabbit-Polyclonal (1:200, Signalway Antibody, Cat No. 46591), anti-DPPA2-Rabbit-Polyclonal (1:1000, Signalway Antibody, Cat No. 62249), anti-Calretinin-Rabbit-Polyclonal (1:500, EpiZyme, Cat No. P011307), anti-p57 Kip2-Rabbit-Monoclonal (1:500, Zenbio, Cat No. R380868), anti-L1TD1-Rabbit-Polyclonal (1:1000, Signalway Antibody, Cat No. 62248), anti-WNT7A-Rabbit-Polyclonal (1:1000, Signalway Antibody, Cat No. #38653-1), anti-GRIK2-Rabbit-Monoclonal (1:500, Zenbio, Cat No. R389225), anti-ROBO2-Rabbit-Polyclonal (1:1000, Proteintech, Cat No. 21635-1-AP), anti-β-actin-Rabbit-Polyclonal (1:2000, Proteintech, Cat No: 20536-1-AP), anti-GAPDH-Mouse-Polyclonal (1:5000, EpiZyme, Cat No. LF205). .. The secondary antibodies include horseradish peroxidase (HRP)-conjugated Goat anti-Rabbit IgG (H + L) (1:2000, Abclonal, Cat No. A5014) or HRP-conjugated Goat anti-Mouse IgG (H + L) (1:5000, Proteintech, Cat No. SA0000-1-1).



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    Signaling pathways of Garrya flavescens extract under LPS treatment in microglia. ( A ) Western blot analysis of BV-2 cells pre-treated with vehicle or GF, followed by LPS treatment at 10, 30 and 60 min. Antibodies against phosphorylated ERK, p38, AKT and <t>β-Actin</t> were used. ( B – D ) Quantitative analysis of the band intensities: p-ERK/β-Actin ( B ), p-p38/β-Actin ( C ), and p-AKT/β-Actin ( D ). * p < 0.05; ** p < 0.01; Student’s t -test. N = 3 independent cultures. Bars indicate mean ± SD. Abbreviations: GF, Garrya flavescens ; LPS, lipopolysaccharide; CGA, chlorogenic acid; ERK, extracellular signal-regulated kinase; p38, p38 mitogen-activated protein kinase; AKT, protein kinase B; β-actin, beta-actin.
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    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with <t>β-actin</t> used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.
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    ABclonal Biotechnology rabbit polyclonal anti β actin
    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with <t>β-actin</t> used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.
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    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with <t>β-actin</t> used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.
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    Proteintech rabbit polyclonal anti β actin
    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with <t>β-actin</t> used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.
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    Proteintech rabbit antibodies against β actin
    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with <t>β-actin</t> used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.
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    Image Search Results


    Signaling pathways of Garrya flavescens extract under LPS treatment in microglia. ( A ) Western blot analysis of BV-2 cells pre-treated with vehicle or GF, followed by LPS treatment at 10, 30 and 60 min. Antibodies against phosphorylated ERK, p38, AKT and β-Actin were used. ( B – D ) Quantitative analysis of the band intensities: p-ERK/β-Actin ( B ), p-p38/β-Actin ( C ), and p-AKT/β-Actin ( D ). * p < 0.05; ** p < 0.01; Student’s t -test. N = 3 independent cultures. Bars indicate mean ± SD. Abbreviations: GF, Garrya flavescens ; LPS, lipopolysaccharide; CGA, chlorogenic acid; ERK, extracellular signal-regulated kinase; p38, p38 mitogen-activated protein kinase; AKT, protein kinase B; β-actin, beta-actin.

    Journal: Plants

    Article Title: Anti-Inflammatory Properties of Garrya flavescens : Phytochemical Profiling and Mitigation of LPS-Induced Neuroinflammation via ERK Signaling and Mitochondrial Modulation

    doi: 10.3390/plants15091319

    Figure Lengend Snippet: Signaling pathways of Garrya flavescens extract under LPS treatment in microglia. ( A ) Western blot analysis of BV-2 cells pre-treated with vehicle or GF, followed by LPS treatment at 10, 30 and 60 min. Antibodies against phosphorylated ERK, p38, AKT and β-Actin were used. ( B – D ) Quantitative analysis of the band intensities: p-ERK/β-Actin ( B ), p-p38/β-Actin ( C ), and p-AKT/β-Actin ( D ). * p < 0.05; ** p < 0.01; Student’s t -test. N = 3 independent cultures. Bars indicate mean ± SD. Abbreviations: GF, Garrya flavescens ; LPS, lipopolysaccharide; CGA, chlorogenic acid; ERK, extracellular signal-regulated kinase; p38, p38 mitogen-activated protein kinase; AKT, protein kinase B; β-actin, beta-actin.

    Article Snippet: Rabbit anti-β-actin antibody (bs-0061R) was obtained from Bioss (Beijing, China).

    Techniques: Protein-Protein interactions, Western Blot

    Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with β-actin used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.

    Journal: Biomedicines

    Article Title: Ionic Extracts of Magnesium Powders Promote In Vitro Lymphangiogenesis

    doi: 10.3390/biomedicines14040913

    Figure Lengend Snippet: Effects of magnesium extracts on lymphangiogenesis-related gene and protein expression in LECs. ( A ) Relative Vegfa mRNA expression levels in LECs treated with Control, Mg (1:10), Mg (1:100), and Mg (1:1000), as determined by qRT-PCR. ( B ) Relative Vegfc mRNA expression levels in LECs under the same treatment conditions. ( C ) Representative Western blot images showing VEGFA and VEGFC protein expression in LECs after treatment with different concentrations of magnesium extracts, with GAPDH used as the internal loading control. ( D ) Additional Western blot analysis showing VEGFR3 protein expression under the same treatment conditions, with β-actin used as the internal loading control. Data in ( A , B ) are presented as the mean ± SD ( n = 3). Statistical analysis for ( A , B ) was performed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Statistical significance is indicated as * p < 0.05, ** p < 0.01; ns, not significant.

    Article Snippet: The primary antibodies used in this study included anti-VEGFA rabbit polyclonal antibody (ZEN-BIOSCIENCE Co., Ltd., Chengdu, China), anti-VEGFC rabbit polyclonal antibody (ZEN-BIOSCIENCE Co., Ltd., Chengdu, China), anti-VEGFR3 rabbit polyclonal antibody (Affinity Biosciences, Shanghai, China), anti-GAPDH rabbit polyclonal antibody (Affinity Biosciences, Shanghai, China), and anti-β-actin rabbit polyclonal antibody (Affinity Biosciences, Shanghai, China).

    Techniques: Expressing, Control, Quantitative RT-PCR, Western Blot