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Acrylamide bis solution

Manufactured by Serva Electrophoresis
Sourced in Germany

Acrylamide/bis solution is a pre-prepared mixture used in the preparation of polyacrylamide gels for electrophoresis. The solution contains acrylamide and N,N'-methylenebisacrylamide (bis) in a specific ratio, which allows for the formation of a cross-linked polyacrylamide matrix when polymerized.

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2 protocols using acrylamide bis solution

1

Synthesis and Characterization of Hydrogel Scaffolds

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Potassium dihydrogen phosphate and silver nitrate were obtained from Merck (Darmstadt, Germany). Di-sodium hydrogen phosphate, acetone, sodium dodecyl sulfate, tris(hydroxymethyl)aminomethane, acetic acid, sodium carbonate, ammonium persulfate, tetramethylenediamine, sodium chloride, sodium thiosulfate and poly(ethylene glycol) (PEG, Mn = 6000 g mol−1) were obtained from Carl Roth (Karlsruhe, Germany). Uranyl acetate and acrylamide/bis solution, 37.5 : 1 were purchased from Serva (Heidelberg, Germany). Spurr Low Viscosity Embedding Kit was obtained from Polysciences (Washington, USA). Poly(ethylene glycol) diacrylate (PEG-DA, Mn = 700 g mol−1) and formaldehyde were obtained from Sigma-Aldrich (Merck; Darmstadt, Germany). The radical photoinitiator 1-[4-(2-hydroxyethoxy)phenyl]-2-hydroxy-2-methyl-1-propan-1-one (Irgacure 2959) was a kind gift from Bodo Möller Chemie GmbH (Offenbach, Germany). A Micro BCA Protein Assay Kit was obtained from Thermo Scientific (Waltham, USA). All chemicals and reagent were used as received. Stock solutions containing 28 mg Irgacure 2959 in 3.972 g SPP buffer were obtained by gentle heating with a heat gun at 100 °C until all material was dissolved, and subsequent cooling to room temperature. Water was withdrawn from a Barnstead GenPure xCAD water purification system (Thermo Scientific, Waltham, USA).
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2

Protein-DNA Conjugation Protocol

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Thrombin from human plasma and apo-transferrin were purchased from Sigma-Aldrich (USA). BSA and fibrinogen from human plasma were purchased from Wako Pure Chemicals Industries (Japan). All ssDNAs, except for the random ssDNA library with its primer set, were synthesized by Sigma-Aldrich (USA). 2-Morpholinoethanesulfonic acid (MES; Wako, Japan), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimido hydrochloride (EDC; Wako, Japan), Dulbecco’s PBS(−) (Wako, Japan), 10% Tween 20 solution (Bio-Rad, USA), tris(hydroxymethyl)aminomethane (Tris; Wako, Japan), 1 M sodium chloride solution (Wako, Japan), 1 M magnesium chloride solution (Wako, Japan), 1 M sodium hydroxide solution (Agilent Technologies, USA), 0.5 M borate buffer at pH 8.5 ± 0.2 (Polysciences, USA), EDTA disodium salt dihydrate (Wako, Japan), and boric acid (Wako, Japan) were used as received. All solutions were prepared using ultrapure water from a Milli-Q water purification system (Merck Millipore, USA). For the preparation of gels, a 37.5:1 (40%, w/v) acrylamide/bis solution, 2.6% C (Serva Electrophoresis, Germany), ammonium persulphate (Bio-Rad, USA), and N,N,N’,N’-tetramethylethylene (TEMED; Bio-Rad, USA) were used. The loading buffer and a 25-bp DNA stepladder were purchased from Wako (Japan).
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