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RLGS protocol
作者:未知 来源:本站原创 时间:2005-7-9
  • Rinse the precipitates with 99.5% ethanol.
  • Dry up the precipitates.
  • Dissolve the precipitate in 300 ul dH2O (or 1/10 x TE) containing 0.5 ul RNase-It (Stratagene).
  • Estimate the DNA concentration (by agarose gel electrophoresis with Etidium bromide or by Hoefer Dyna Quant 200) and make a solution adjusted at 750 ng/ul for RLGS analysis in this plant.
  • Ascertain the size of obtained DNA fragments are larger than lamda DNA using 0.5 % agarose gel electrophoresis (100 - 200 kb recommended).
     

    B. Preparation of gel holder

  • Cut teflon-tubing (NICHIAS AWG-11, inner diameter: 2.4 mm) into 65 cm (cut a top at an angle of about 20 degrees) for gel holder.
  • insert it into a glass tube from the bottom, and then a sharp tip of the tubing may exert form the top.
  • Pull out the tip about 2 cm with a plier.
  • Cut off the  top of the tubing leaving about 1 mm in height.
  • Push the top of the tubing onto a heated tip of a hand welder.
  • After a few seconds, push the top of the tubing onto a flat and smooth surface.
  • Cut off the tubing at the bottom to adjust the length of the gel holder to 62 cm.
     

    C. Preparation of 1-D Gel

  • Connect a 5 ml plastic syringe fitted with a three-way stopcock and the gel holder with 3 cm of silicon tubing.
  • Suck up the gel solution gradually to reach the height of 61 cm, and tap on the glass by a finger.
  • Close the stopcock and set it on a double buret clamp on a support stand.
  • Wait 10 min. to solidify the gel.
  • Turn the stopcock to make air free.
  • Remove the stopcock and silicon tubing.
  • If the gel does not reach the height of 61 cm, put on the gel solution up to the height of 61 cm using a 1 ml syringe with L-needle (19 gauge, right angle cut, 5 cm long) and wait 10 min.
  • Put 1-D buffer containing 20% sucrose on the gel to avoid drying.
  • Add 350 ml of 1x 1-D buffer to anodal tank (bottom) and fix the gels on the apparatus (Bio-craft) .
     

    D. Not I and EcoR V digestion

     
  • Mix the reaction solution mildly but completely with pipetting.
  • Centrifuge at 6,000 rpm for 1 min.
  • Incubate at 37oC for 3 hrs.
     

    E. Labelling

  • Mix a 10 ul DNA sample with a 3.2 ul labelling solution gently with pipetting ten times.
  • Incubate at 27oC for 30 min.
  • Add 3 ul Stop solution.
  • Fill the cathodal tank (top) with 300 ml of 1x 1-D buffer.
  • Wash out the 1-D buffer containing 20% sucrose from the top of the gel.
  • Apply 10 ul (about 0.15 ug DNA for rice, or about 0.45 ug DNA for egg plant) sample on a 1-D gel.
  • Run electrophoresis at 130 Volts (120 - 140 Volts) for 40 hrs (until the center of BPB reaches 40 cm and that of XC reaches 19 cm from the top of the gel)(Photo) .
     
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