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BlueNativeGelElectrophoresis

Blue Native Gel ElectrophoresisStock solutions49.5%T, 3%C Acrylamide 24 g acrylamide, 0.75 g bisacrylamide / 50 ml H2O Store at RT3 x Gel buffer 150 mM BisTris-HCl, 1.5 M 6-amino-caproic acid, pH 7.0 Adjust pH to 7.0 with HCl at 4°C Store at 4°C75% (w/v) Glycerol Store at 4°C10 x Cathode buffer 0.5 M Tricine, 150 mM BisTris No need to adjust pH Store at 4°C5 x Anode buffer 0.25 M BisTris-HCl, pH 7.0 Adjust pH to 7.0 ......阅读全文

Blue Native Gel Electrophoresis

Blue Native Gel ElectrophoresisStock solutions49.5%T, 3%C Acrylamide 24 g acrylamide, 0.75 g bisacrylamide / 50 ml H2O Store at RT3 x Gel buffer 150 m

Native gel electrophoresis(非变性电泳)

Native gel electrophoresis Under native PAGE conditions, polypeptides retain their higher-order structure and often retain enzymatic activity and inte

Agarose gel electrophoresis

General Procedure Cast a gel Place it in gel box in running buffer Load samples Run the gel Image the gel Casting Gels 0.7% ag

Gel Electrophoresis of DNA

What is Electrophoresis? Electrophoresis is a technique used in the laboratory that results in the separation of charged molecules. In this CyberLab

Agarose Gel Electrophoresis

实验概要 Separating nucleic acid fragments by agarose gel electrophoresis. 实验原理   Agarose  gel electrophoresis remains the most widely used technique

RNA gel electrophoresis

实验概要RNA gel electrophoresis主要试剂DEPC H2ODEPC 0.1% (v/v)q.s. de-ioinized H2O37ºC x1 hr, or r.t. overnightAutoclave.(NaOAc, EDTA and ethidium bromide sol

RNA gel electrophoresis

MaterialsDEPC H2ODEPC 0.1% (v/v)q.s. de-ioinized H2O37ºC x1 hr, or r.t. overnightAutoclave.(NaOAc, EDTA and ethidium bromide solutions should also be

Alkaline agarose gel electrophoresis

Alkaline agarose gel electrophoresis (Sambrook et al., 1989) Alkaline agarose gels can be used to determine the size and quality of first and second

Polyacrylamide Gel Electrophoresis of Oligonucleotides

1. Pour and polymerize a 20% polyacrylamide gel, no Urea. 2. Remove clamps. Rinse with water. Remove comb. Rinse top of gel well. 3. Insert comb te

Agarose Gel Electrophoresis of DNA

1) Dissolve 1 g of agarose in 100 ml of 1X TAE or TBE buffer (gives a 1% gel). See note for making LMP agarose gel. 2) Cast the gel with the comb in p