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Top : New Forum Archives (2009-): : Electrophoresis
31. How to make gradient gel (10-20%), how to control the speed of flow? - (reply: 4)
32. Straight bands on DNA gel - (reply: 3)
33. Western blot- bands weak - (reply: 10)
34. western blotting troubleshooting - (reply: 2)
35. Application for calculating ELFO fragment length - (reply: 1)
36. Plasmides run higher than marker - (reply: 4)
37. Odd Bands on Gel - (reply: 3)
38. Agarose gell electrophoresis - (reply: 1)
39. Elchrom Origins - (reply: 1)
40. Pattern/cloud appearing on agarose gel - (reply: 15)
41. TBE buffer-what is the role of each component? - (reply: 1)
42. Problems with having to run the gels for so long - (reply: 14)
43. Ethidium Bromide Agarose Gel Hazard - (reply: 6)
44. Single Plasmid Gel Band - (reply: 1)
45. Buffer in Gel - (reply: 6)
46. agarose gel electrophoresis - (reply: 5)
47. Uneven bands denaturing agarose - (reply: 2)
48. What gel percent and Voltage is needed to separate 2680bp and 2600bp DNA nicely - (reply: 7)
49. Smear on agarose gel from QIAGEN extracted plant samples - (reply: 1)
50. E gels and the E gel opener - (reply: 1)
51. Why do we use sponges in the Western Transfer? - (reply: 5)
52. Non-hazardous substitute for ethidium bromide? - (reply: 17)
53. What causes surface fluorescence on agarose gels? - (reply: 6)
54. Problems with PAGE gels - (reply: 1)
55. carpet in gels for PCR products - (reply: 2)
56. Native blue page - (reply: 1)
57. What % native urea gel do I use for Fab and F(ab')2? - (reply: 2)
58. protein extraction from GEL - (reply: 5)
59. Problem with visibility on third comb in gels - (reply: 4)
60. Secondary Ab is M.I.A. ... how long can I leave my membrane in wash buffer? - (reply: 1)

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