Blue native PAGE | Nature Protocols
27/6/2006 · Schägger, H. & von Jagow, G. Tricine-sodium dodecyl sulfate polyacrylamide gel electrophoresis for the separation of proteins in the range from 1–100 kDalton. Anal. Biochem. 166 , 368–379 (1987).
Protein interface redesign facilitates the transformation of nanocage building blocks to 1D and 2D nanomaterials | Nature Communications
11/8/2021 · For native PAGE, a 4–20% polyacrylamide gradient gel was used and run at 5 mA for 10 h at 4 C. Gels were stained with Coomassie brilliant blue R250. High-resolution gel filtration chromatography
Reliable cation polyacrylamide cpam for Garments
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10X SDS MES Running Buffer for SDS-PAGE Gel Electrophoresis
5/3/2021 · 10X SDS MES Running Buffer for SDS-PAGE Gel Electrophoresis 1 Liter SDS MES Running Buffer sharpens the protein bands and get better resolution for small size proteins than the conventional. SDS MES running buffer is used for electrophoresis
10x Tris-Glycine-SDS Running Buffer (10xTGS buffer, 1L-10L)
1xTGS (After dilution): Tris 25 mM, Glycine 192 mM, 0.1%SDS, pH 8.3, Western blot running buffer. Tris-glycine-SDS (TGS) running buffer is the most commonly used buffer for sodium dodecyl sulfate – polyacrylamide gel electrophoresis (SDS-PAGE)
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6x Green Fluorescent DNA Loading Dye (1.0 ml, for UV & Blue LED light)
There is no need to add safe DNA gel stain or other fluorescent dye to the gel or running buffer. After the electrophoresis, the green DNA bands could be viewed under UV light and Blue LED light. Storage: Store at 4 °C. Shelf life: Two years
10x Tris Borate EDTA (10x TBE buffer, 1L-10L)
1x TBE (After dilution): Tris 89 mM, Boric acid 89 mM, EDTA 2 mM, pH 8.3. To prepare 1X TBE buffer add 100 ml of 10X TBE buffer to 900 ml of deionized water and mix well. Use fresh 1X TBE both for the gel and for the electrophoresis run.
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