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Top : New Forum Archives (2009-): : Electrophoresis
61. Plasmides run higher than marker - (reply: 4)
62. Odd Bands on Gel - (reply: 3)
63. Agarose gell electrophoresis - (reply: 1)
64. Elchrom Origins - (reply: 1)
65. Pattern/cloud appearing on agarose gel - (reply: 15)
66. TBE buffer-what is the role of each component? - (reply: 1)
67. Problems with having to run the gels for so long - (reply: 14)
68. Ethidium Bromide Agarose Gel Hazard - (reply: 6)
69. Single Plasmid Gel Band - (reply: 1)
70. Buffer in Gel - (reply: 6)
71. agarose gel electrophoresis - (reply: 5)
72. Uneven bands denaturing agarose - (reply: 2)
73. What gel percent and Voltage is needed to separate 2680bp and 2600bp DNA nicely - (reply: 7)
74. Smear on agarose gel from QIAGEN extracted plant samples - (reply: 1)
75. E gels and the E gel opener - (reply: 1)
76. Why do we use sponges in the Western Transfer? - (reply: 5)
77. Non-hazardous substitute for ethidium bromide? - (reply: 17)
78. What causes surface fluorescence on agarose gels? - (reply: 6)
79. Problems with PAGE gels - (reply: 1)
80. carpet in gels for PCR products - (reply: 2)
81. Native blue page - (reply: 1)
82. What % native urea gel do I use for Fab and F(ab')2? - (reply: 2)
83. protein extraction from GEL - (reply: 5)
84. Problem with visibility on third comb in gels - (reply: 4)
85. Secondary Ab is M.I.A. ... how long can I leave my membrane in wash buffer? - (reply: 1)
86. Product help: Inexpensive Agarose Gel - (reply: 1)
87. what is your DNA concentration after gel extraction? - (reply: 5)
88. RNase h electrophoresis - (reply: 1)
89. Using 4-year old precast gels - (reply: 4)
90. Why do supposedly sharp bands sometimes appear unclear in agarose gel? - (reply: 1)

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