sin3a (Proteintech)
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sin3a
Sin3a, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+sin3a+antibody/SIN3A+Antibody/pm41663400-400-56-57
Average 93 stars, based on 12 article reviews
Sin3a, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+sin3a+antibody/SIN3A+Antibody/pm41663400-400-56-57
Average 93 stars, based on 12 article reviews
sin3a - by Bioz Stars,
2026-09
93/100 stars
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Expressing:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Quantitative Proteomics:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Immunofluorescence:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Control:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Functional Assay:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The In Vitro:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Flow Cytometry:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Cell Culture:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Knockdown:Article Title: Counteracting FOX proteins epigenetically control the herpesvirus lytic-latent balance Article Snippet: Proteins were resolved on 10–12% SDS-polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore #IPVH00010) before being probed with the following antibodies at the following dilutions.. Primary antibodies: anti-Flag M2 antibody (1:2000, sigma #F1804); anti-HA antibody (1:2000, Sangon Biotech #D110004-0100); anti-actin antibody (1:10000, ABclonal #AC026); anti-H3 antibody (1:2000, Solarbio #K200033M); anti-FOXK1 antibody (1:1000, invitrogen PA5-36257); anti-FOXK2 antibody (1:1000, ABclonal #A14245); anti-CREBBP antibody (1:1000, Cell Signaling Technology #7389 s); anti-H3K27ac antibody (1:2000, Abcam #ab4729); anti-ARID1A antibody (1:2000, Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The Anti- Article Title: Identification of SIN3A as a Promising Epigenetic Target Against Allergic Rhinitis Article Snippet: Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.Proteins were separated via SDS-PAGE, electrotransferred to a PVDF membrane, treated with a primary antibody at 4°C overnight, washed three times, incubated with a secondary antibody for one hour at room temperature, and detected using chemiluminescent reagents.. The |
