chip dna clean concentrator kit (Zymo Research)
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Chip Dna Clean Concentrator Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 99/100, based on 1500 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/pmc13109728-100-15-21
Average 99 stars, based on 1500 article reviews
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Chromatin Immunoprecipitation:Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha Article Snippet: HiYield Gel/PCR DNA Fragments Extraction Kit , RBC Bioscience , Cat#YDF300. .. Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3–UPF1 splicing and surveillance axis Article Snippet: .. Samples were then treated with 400 μg/mL RNase A (Thermo Fisher, #EN0531) at 37 °C for 45 min, followed by protein digestion with 200 μg/mL protease K—50 mM Tris–HCl at pH 7.5 and 10 mM EDTA—at 65 °C for 1 h. DNA was purified using Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha. Article Snippet: .. Note: This protocol used the Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha Article Snippet: .. Note: This protocol used the Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice. Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using Purification:Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3–UPF1 splicing and surveillance axis Article Snippet: .. Samples were then treated with 400 μg/mL RNase A (Thermo Fisher, #EN0531) at 37 °C for 45 min, followed by protein digestion with 200 μg/mL protease K—50 mM Tris–HCl at pH 7.5 and 10 mM EDTA—at 65 °C for 1 h. DNA was purified using Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice. Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using Sonication:Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo other:Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3-UPF1 splicing and surveillance axis. Article Snippet: Supernatants were diluted 5-fold with immunoprecipitation (IP) dilution buffer—20 mM Tris-HCl at pH 8.0, 150 mM NaCl, 1 mM EDTA, and 1% Triton X-100—and incubated overnight at 4°C with anti-FLAG-M2 affinity gel (Sigma, #A2220). Incubation:Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice. Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using |
