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anti actin antibody sc 1615  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology anti actin antibody sc 1615
    Anti Actin Antibody Sc 1615, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 22508 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/actin+sc+1615/Actin+Antibody/us12559863-828-12-15
    Average 96 stars, based on 22508 article reviews
    anti actin antibody sc 1615 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation.
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Cell line-dependent difference in glutathione levels affects the cigarette sidestream smoke-induced inhibition of nucleotide excision repair.
    Article Snippet: We recently reported that cigarette sidestream smoke (CSS) induced inhibition of nucleotide excision repair (NER) and the cause was NER molecule degradation by aldehydes contained in CSS [Carcinogenesis 39, 56–65, 2018; Mutat.. Res.. 834, 42–50, 2018].

    Incubation:

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation.
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Cell line-dependent difference in glutathione levels affects the cigarette sidestream smoke-induced inhibition of nucleotide excision repair.
    Article Snippet: We recently reported that cigarette sidestream smoke (CSS) induced inhibition of nucleotide excision repair (NER) and the cause was NER molecule degradation by aldehydes contained in CSS [Carcinogenesis 39, 56–65, 2018; Mutat.. Res.. 834, 42–50, 2018].

    Expressing:

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation.
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation
    Article Snippet: The treated cells were scraped, pelleted, suspended in lysis buffer (100 mM Tris-HCl (pH 8.0), 50 mM EDTA, 0.5% Triton X-100) containing protease inhibitors (Wako #161-26023), sonicated for 30 s, mixed with an equal volume of 2x sample buffer (0.1 M Tris-HCl (pH6.8), 4% SDS, 20% glycerol, 12% 2-mercaptoethanol, 0.004% bromophenol blue), and boiled for 5 min. Proteins were separated by 10 or 15% polyacrylamide gels and transferred to polyvinylidene fluoride membranes. .. After blocking with 0.2% skim milk or albumin, membranes were incubated with primary antibodies against global N-terminal acetyl-histone H3 (#06-599), acetyl-histone H3 (Lys 9) (#06-942), acetyl-histone H3 (Lys 14) (#06-911) (Merck Millipore, Burlington, MA), MMP-1 (GTX100534) (GeneTex, Alton Pkwy Irvine, CA), and actin (sc-1615) (Santa Cruz Biotechnology, Dallas, TX) overnight at 4°C, then incubated with secondary antibody conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, PA) for 2 h. Protein expression was visualized with an enhanced chemiluminescence plus detection kit (Thermo Fisher Scientific, Waltham, MA). ..

    Article Title: Cell line-dependent difference in glutathione levels affects the cigarette sidestream smoke-induced inhibition of nucleotide excision repair.
    Article Snippet: We recently reported that cigarette sidestream smoke (CSS) induced inhibition of nucleotide excision repair (NER) and the cause was NER molecule degradation by aldehydes contained in CSS [Carcinogenesis 39, 56–65, 2018; Mutat.. Res.. 834, 42–50, 2018].

    other:

    Article Title: Emetine exerts anticancer effects in U2OS human osteosarcoma cells via activation of p38 and inhibition of ERK, JNK, and β-catenin signaling pathways.
    Article Snippet: Funding information Ministry of Education Korea, Grant/Award Number: NRF‐ 2018R1D1A1B07040998 Abstract Osteosarcoma (OS) is a primary bone neoplasm that is highly malignant.. As advances in chemotherapy for the treatment of OS have stagnated, discovery of new reagents is required.. Emetine is a phytochemical which can be isolated from a medicinal herb Cephaelis ipecacuanha and is traditionally used for amoebicides.

    Article Title: The Metabolism of 2-arachidonoylglycerol in Rod Outer Segments Is Modulated by Proteins Involved in the Phototransduction Process.
    Article Snippet: We previously reported that 2-arachidonoylglycerol (2-AG) synthesis by diacylglycerol lipase (DAGL) and lysophosphatidate phosphohydrolase (LPAP) and hydrolysis by monoacylglycerol lipase (MAGL) in rod outer segments (ROS) from bovine retina were differently modified by light applied to the retina.. Based on these findings, the aim of the present research was to evaluate whether 2-AG metabolism could be modulated by proteins involved in the visual process.. To this end, ROS kept in darkness (DROS) or obtained in darkness and then subjected to light (BROS) were treated with GTPγS and GDPβS, or with low and moderate ionic strength buffers for detaching soluble and peripheral proteins, or soluble proteins, respectively.



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