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Millipore monoclonal anti β actin antibody
Monoclonal Anti β Actin Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/monoclonal anti β actin antibody/product/Millipore
Average 99 stars, based on 1 article reviews
Price from $9.99 to $1999.99
monoclonal anti β actin antibody - by Bioz Stars, 2021-03
99/100 stars

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Immunostaining:

Article Title: Interleukin-6 contributes to CNS axon regeneration upon inflammatory stimulation
Article Snippet: The blots were blocked either in 5% dried milk or in 2% ECL Advance blocking agent in Tris-buffered saline-Tween-20. .. They were then processed for immunostaining with either an antiserum against rat phospho-STAT3 (Tyr705; Cell Signaling; 1 : 5000), a monoclonal antibody against rat β -actin (Sigma; 1 : 7500), or a polyclonal antibody against the IL-6 receptor (R & D Systems; 1 : 6000) that was either preadsorbed to a cell-lysate from IL-6 receptor overexpressing HEK 293 cells (pread) or control HEK 293 cells (MOCK) at 4 °C overnight. .. Bound antibodies were visualized with anti-rabbit, anti-goat or anti-mouse immunoglobulin G (IgG) secondary antibodies conjugated with horseradish peroxidase diluted to 1 : 80 000 (all Sigma Holland).

Incubation:

Article Title: Inhibition of Steroid Receptor Coactivator-1 Blocks Estrogen and Androgen Action on Male Sex Behavior and Associated Brain Plasticity
Article Snippet: The primary antibody was visualized with a secondary goat antibody coupled to horseradish peroxidase (1:1000; Amersham Biosciences), and the peroxidase activity was revealed with the enhanced chemiluminescence system (ECL; Amersham Biosciences). .. The membranes were then stripped, extensively rinsed, and incubated for 1 h at room temperature with a monoclonal β-actin antibody (1:10,000; clone AC-74; Sigma) that was subsequently visualized as described above. ..

SDS Page:

Article Title: Inhibiting the integrated stress response pathway prevents aberrant chondrocyte differentiation thereby alleviating chondrodysplasia
Article Snippet: .. The lysate was subjected to SDS-PAGE under reducing conditions and probed with ATF4, BiP (ADI-SPA-826, Enzo) and beta-actin (A2228, Sigma) antibody. .. Luciferase assays were conducted using a dual luciferase reporter assay kit (Promega), according to the manufacturer’s protocol.

other:

Article Title: Tra2-Mediated Recognition of HIV-1 5? Splice Site D3 as a Key Factor in the Processing of vpr mRNA
Article Snippet: A mouse antibody against α-actin (A2228) was obtained from Sigma-Aldrich.

Produced:

Article Title: Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
Article Snippet: Purified mouse anti-p53 antibody (#554169) was acquired from Becton, Dickinson and Company (B & D) (United States). .. Monoclonal anti-β-actin antibody produced in mouse was obtained from Sigma-Aldrich (#A2228, United States). .. Secondary polyclonal anti-goat, anti-rabbit and anti-mouse antibodies labeled with horseradish peroxidase were purchased in Sigma-Aldrich, Corp. (United States).

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    Millipore mouse anti β actin
    K562 cells with ectopic HD5 expression. (A) Screening of cell lines for endogenous HD5 expression. HD5 mRNA levels were measured in total cellular RNA by qRT-PCR and expressed as percentages of <t>β-actin</t> (Act B) mRNA levels. (B) HD5 mRNA expression
    Mouse Anti β Actin, supplied by Millipore, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti β actin/product/Millipore
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse anti β actin - by Bioz Stars, 2021-03
    97/100 stars
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    K562 cells with ectopic HD5 expression. (A) Screening of cell lines for endogenous HD5 expression. HD5 mRNA levels were measured in total cellular RNA by qRT-PCR and expressed as percentages of β-actin (Act B) mRNA levels. (B) HD5 mRNA expression

    Journal: Journal of Virology

    Article Title: Studies on the Interaction of Tumor-Derived HD5 Alpha Defensins with Adenoviruses and Implications for Oncolytic Adenovirus Therapy

    doi: 10.1128/JVI.02030-16

    Figure Lengend Snippet: K562 cells with ectopic HD5 expression. (A) Screening of cell lines for endogenous HD5 expression. HD5 mRNA levels were measured in total cellular RNA by qRT-PCR and expressed as percentages of β-actin (Act B) mRNA levels. (B) HD5 mRNA expression

    Article Snippet: After blots were stripped with Restore Western blot striping buffer (Thermo Scientific, Waltham, MA), they were incubated with mouse anti-β-actin (Sigma, St. Louis, MO) (1:5,000).

    Techniques: Expressing, Quantitative RT-PCR, Activated Clotting Time Assay

    ShRNA plasmid design and in vitro LGI1-shRNA downregulation. A) shRNA construct: LGI1-shRNA is under the promoter mU6 (murine U6 small-non-coding-RNA), meanwhile the EGFP (enhanced green fluorescent protein) is under the independent promoter PGK (phosphoglycerate kinase). NeoR/KanR (Neomycin/Kanamycin Resistance). B) LGI1 expression in neuronal cultures. The first lane is the endogenous level of LGI1 in untreated primary cultures, the second lane shows the levels of LGI1 in cultures transduced with scramble virus and the fourth and last lane shows the levels of LGI1 in cultures transduced with shRNA-LGI1. The β-actin and EGFP signals are also shown. EGFP intensity was detected to evaluate that the reporter gene was also expressed at the same time as the shRNA and hence could be a reliable source of transduction rate. C) Quantification of LGI1 concentrations detected by the western blot method. p=0.005 two-tailed Student’s t-test (blots n=5 from 5 distinct preparations).

    Journal: bioRxiv

    Article Title: LGI1 downregulation increases neuronal circuit excitability

    doi: 10.1101/2019.12.17.879833

    Figure Lengend Snippet: ShRNA plasmid design and in vitro LGI1-shRNA downregulation. A) shRNA construct: LGI1-shRNA is under the promoter mU6 (murine U6 small-non-coding-RNA), meanwhile the EGFP (enhanced green fluorescent protein) is under the independent promoter PGK (phosphoglycerate kinase). NeoR/KanR (Neomycin/Kanamycin Resistance). B) LGI1 expression in neuronal cultures. The first lane is the endogenous level of LGI1 in untreated primary cultures, the second lane shows the levels of LGI1 in cultures transduced with scramble virus and the fourth and last lane shows the levels of LGI1 in cultures transduced with shRNA-LGI1. The β-actin and EGFP signals are also shown. EGFP intensity was detected to evaluate that the reporter gene was also expressed at the same time as the shRNA and hence could be a reliable source of transduction rate. C) Quantification of LGI1 concentrations detected by the western blot method. p=0.005 two-tailed Student’s t-test (blots n=5 from 5 distinct preparations).

    Article Snippet: The following antibodies and dilutions were used: 1:250 polyclonal goat-anti-LGI1 (Santa Cruz, c-19), 1:4000 monoclonal mouse-anti β-actin (Sigma), 1:1000 rabbit-anti-GFP (Abcam ab6556).

    Techniques: shRNA, Plasmid Preparation, In Vitro, Construct, Expressing, Transduction, Western Blot, Two Tailed Test

    Effects of various concentrations of the resveratrol on KGN cells. Cells were incubated with resveratrol at 0, 10, 25, 50, and 100 μmol/L for 24 h. A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Journal: Reproductive Medicine and Biology

    Article Title: Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia, et al. Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia

    doi: 10.1002/rmb2.12323

    Figure Lengend Snippet: Effects of various concentrations of the resveratrol on KGN cells. Cells were incubated with resveratrol at 0, 10, 25, 50, and 100 μmol/L for 24 h. A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Article Snippet: Blots were then incubated for 1 hour at room temperature (25°C) with rabbit monoclonal SIRT1 antibody (1:400; Santa Cruz Biotechnology, Inc), rabbit monoclonal HIF‐1a antibody (1:1000; Epitomics), or mouse monoclonal β‐actin antibody (1:5000; Sigma‐Aldrich) as the primary antibody, and anti‐rabbit immunoglobulin IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) or anti‐mouse IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) as the secondary antibody.

    Techniques: Incubation, Real-time Polymerase Chain Reaction, Western Blot, Enzyme-linked Immunosorbent Assay

    Protective effects of resveratrol against CoCl 2 ‐induced hypoxic stress. KGN cells were cultured in medium containing 100 μmol/L CoCl 2 with or without the 50 μmol/L resveratrol. A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control protein. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Journal: Reproductive Medicine and Biology

    Article Title: Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia, et al. Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia

    doi: 10.1002/rmb2.12323

    Figure Lengend Snippet: Protective effects of resveratrol against CoCl 2 ‐induced hypoxic stress. KGN cells were cultured in medium containing 100 μmol/L CoCl 2 with or without the 50 μmol/L resveratrol. A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control protein. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Article Snippet: Blots were then incubated for 1 hour at room temperature (25°C) with rabbit monoclonal SIRT1 antibody (1:400; Santa Cruz Biotechnology, Inc), rabbit monoclonal HIF‐1a antibody (1:1000; Epitomics), or mouse monoclonal β‐actin antibody (1:5000; Sigma‐Aldrich) as the primary antibody, and anti‐rabbit immunoglobulin IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) or anti‐mouse IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) as the secondary antibody.

    Techniques: Cell Culture, Real-time Polymerase Chain Reaction, Western Blot, Enzyme-linked Immunosorbent Assay

    Effects of CoCl 2 ‐induced hypoxic stress on mRNA expression and protein secretion. KGN cells were incubated for 24 h in medium containing with 10 μmol/L or 100 μmol/L CoCl 2 . A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Journal: Reproductive Medicine and Biology

    Article Title: Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia, et al. Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia

    doi: 10.1002/rmb2.12323

    Figure Lengend Snippet: Effects of CoCl 2 ‐induced hypoxic stress on mRNA expression and protein secretion. KGN cells were incubated for 24 h in medium containing with 10 μmol/L or 100 μmol/L CoCl 2 . A, SIRT1 mRNA levels were assessed by real‐time PCR and calculated after normalization to EF1α mRNA levels. B, The protein levels of SIRT1 were quantified by Western blotting, and β‐actin was used as the control. C, The protein levels were quantified using ImageJ. D, VEGF protein levels were analyzed by ELISA. E, The mtDNA copy number was determined using real‐time PCR. Fold differences are shown compared with the control, for which the value was defined as 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Article Snippet: Blots were then incubated for 1 hour at room temperature (25°C) with rabbit monoclonal SIRT1 antibody (1:400; Santa Cruz Biotechnology, Inc), rabbit monoclonal HIF‐1a antibody (1:1000; Epitomics), or mouse monoclonal β‐actin antibody (1:5000; Sigma‐Aldrich) as the primary antibody, and anti‐rabbit immunoglobulin IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) or anti‐mouse IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) as the secondary antibody.

    Techniques: Expressing, Incubation, Real-time Polymerase Chain Reaction, Western Blot, Enzyme-linked Immunosorbent Assay

    Effect of resveratrol on HIF‐1α. KGN cells were incubated for 24 h in medium containing 100 μmol/L CoCl 2 with or without 50 μmol/L resveratrol (n = 3). A, The expression of HIF‐1α was quantified by Western blotting. The levels of HIF‐1α were normalized to levels of β‐actin (n = 3). B, The protein levels were quantified using ImageJ. C, VEGF protein levels were analyzed by ELISA. Fold differences are shown compared with the control, for which the value was defined 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Journal: Reproductive Medicine and Biology

    Article Title: Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia, et al. Resveratrol protects mitochondrial quantity by activating SIRT1/PGC‐1α expression during ovarian hypoxia

    doi: 10.1002/rmb2.12323

    Figure Lengend Snippet: Effect of resveratrol on HIF‐1α. KGN cells were incubated for 24 h in medium containing 100 μmol/L CoCl 2 with or without 50 μmol/L resveratrol (n = 3). A, The expression of HIF‐1α was quantified by Western blotting. The levels of HIF‐1α were normalized to levels of β‐actin (n = 3). B, The protein levels were quantified using ImageJ. C, VEGF protein levels were analyzed by ELISA. Fold differences are shown compared with the control, for which the value was defined 1.0. The data are presented as the mean ± SEM, n = 3. Statistically significant differences are indicated by brackets: * P

    Article Snippet: Blots were then incubated for 1 hour at room temperature (25°C) with rabbit monoclonal SIRT1 antibody (1:400; Santa Cruz Biotechnology, Inc), rabbit monoclonal HIF‐1a antibody (1:1000; Epitomics), or mouse monoclonal β‐actin antibody (1:5000; Sigma‐Aldrich) as the primary antibody, and anti‐rabbit immunoglobulin IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) or anti‐mouse IgG peroxidase‐labeled secondary antibody (1:10 000; GE Healthcare Life Science) as the secondary antibody.

    Techniques: Incubation, Expressing, Western Blot, Enzyme-linked Immunosorbent Assay

    Temporal changes in synaptic plasticity-related signals in the mouse hippocampus following methotrexate (MTX) administration. (A) N-methyl-D-aspartic acid receptor 1 (NMDAR1). (B) Calcium/calmodulin-dependent protein kinase II (CaMKII). (C) Extracellular signal-regulated kinase 1/2 (ERK1/2). (D) cAMP responsive element-binding protein (CREB). (E) Glutamate receptor 1 (GluR1). The relative expression levels of phosphorylated (P) and total (T) forms were determined by densitometry and normalized to β-actin signals. Furthermore, to examine the activation levels of each signal, the relative levels of the P forms were normalized to their T-forms. Data are reported as mean ± SEM of three mice per time point. Values for protein expression levels from the hippocampus of vehicle-treated controls were arbitrarily defined as 1 (bar graphs). a P

    Journal: Neural Regeneration Research

    Article Title: Temporal profiles of synaptic plasticity-related signals in adult mouse hippocampus with methotrexate treatment ☆

    doi: 10.3969/j.issn.1673-5374.2012.21.008

    Figure Lengend Snippet: Temporal changes in synaptic plasticity-related signals in the mouse hippocampus following methotrexate (MTX) administration. (A) N-methyl-D-aspartic acid receptor 1 (NMDAR1). (B) Calcium/calmodulin-dependent protein kinase II (CaMKII). (C) Extracellular signal-regulated kinase 1/2 (ERK1/2). (D) cAMP responsive element-binding protein (CREB). (E) Glutamate receptor 1 (GluR1). The relative expression levels of phosphorylated (P) and total (T) forms were determined by densitometry and normalized to β-actin signals. Furthermore, to examine the activation levels of each signal, the relative levels of the P forms were normalized to their T-forms. Data are reported as mean ± SEM of three mice per time point. Values for protein expression levels from the hippocampus of vehicle-treated controls were arbitrarily defined as 1 (bar graphs). a P

    Article Snippet: Membranes were stripped and re-probed with a mouse monoclonal anti-β-actin (1:20 000; Sigma-Aldrich) for normalization.

    Techniques: Binding Assay, Expressing, Activation Assay, Mouse Assay

    Time-response changes of neurotrophic factors in the mouse hippocampus following administration of methotrexate (MTX). (A) Brain-derived neurotrophic factor (BDNF). (B) Glial cell line-derived neurotrophic factor (GDNF). The relative expression levels of proteins were determined by densitometry and normalized to β-actin signals. Data are reported as mean ± SEM. n = 3 mice per time point. Values for protein expression levels from the hippocampus of vehicle-treated controls (Cont) were arbitrarily defined as 1 (bar graphs). a P

    Journal: Neural Regeneration Research

    Article Title: Temporal profiles of synaptic plasticity-related signals in adult mouse hippocampus with methotrexate treatment ☆

    doi: 10.3969/j.issn.1673-5374.2012.21.008

    Figure Lengend Snippet: Time-response changes of neurotrophic factors in the mouse hippocampus following administration of methotrexate (MTX). (A) Brain-derived neurotrophic factor (BDNF). (B) Glial cell line-derived neurotrophic factor (GDNF). The relative expression levels of proteins were determined by densitometry and normalized to β-actin signals. Data are reported as mean ± SEM. n = 3 mice per time point. Values for protein expression levels from the hippocampus of vehicle-treated controls (Cont) were arbitrarily defined as 1 (bar graphs). a P

    Article Snippet: Membranes were stripped and re-probed with a mouse monoclonal anti-β-actin (1:20 000; Sigma-Aldrich) for normalization.

    Techniques: Derivative Assay, Expressing, Mouse Assay