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1. agarose gel electrophoresis of RNA - (reply: 1)
2. EtBr in agarose gel and running buffer - (reply: 3)
3. 15% SDS-PAGE issues - (reply: 4)
4. Protein of 460 kD on western blot - (reply: 3)
5. Help with bad electrophoresis run. - (reply: 3)
6. How to make gradient gel (10-20%), how to control the speed of flow? - (reply: 4)
7. Straight bands on DNA gel - (reply: 3)
8. Western blot- bands weak - (reply: 10)
9. western blotting troubleshooting - (reply: 2)
10. Application for calculating ELFO fragment length - (reply: 1)
11. Plasmides run higher than marker - (reply: 4)
12. Odd Bands on Gel - (reply: 3)
13. Agarose gell electrophoresis - (reply: 1)
14. Elchrom Origins - (reply: 1)
15. Pattern/cloud appearing on agarose gel - (reply: 15)
16. TBE buffer-what is the role of each component? - (reply: 1)
17. Problems with having to run the gels for so long - (reply: 14)
18. Ethidium Bromide Agarose Gel Hazard - (reply: 6)
19. Single Plasmid Gel Band - (reply: 1)
20. Buffer in Gel - (reply: 6)
21. agarose gel electrophoresis - (reply: 5)
22. Uneven bands denaturing agarose - (reply: 2)
23. What gel percent and Voltage is needed to separate 2680bp and 2600bp DNA nicely - (reply: 7)
24. Smear on agarose gel from QIAGEN extracted plant samples - (reply: 1)
25. E gels and the E gel opener - (reply: 1)
26. Why do we use sponges in the Western Transfer? - (reply: 5)
27. Non-hazardous substitute for ethidium bromide? - (reply: 17)
28. What causes surface fluorescence on agarose gels? - (reply: 6)
29. Problems with PAGE gels - (reply: 1)
30. carpet in gels for PCR products - (reply: 2)
2. EtBr in agarose gel and running buffer - (reply: 3)
3. 15% SDS-PAGE issues - (reply: 4)
4. Protein of 460 kD on western blot - (reply: 3)
5. Help with bad electrophoresis run. - (reply: 3)
6. How to make gradient gel (10-20%), how to control the speed of flow? - (reply: 4)
7. Straight bands on DNA gel - (reply: 3)
8. Western blot- bands weak - (reply: 10)
9. western blotting troubleshooting - (reply: 2)
10. Application for calculating ELFO fragment length - (reply: 1)
11. Plasmides run higher than marker - (reply: 4)
12. Odd Bands on Gel - (reply: 3)
13. Agarose gell electrophoresis - (reply: 1)
14. Elchrom Origins - (reply: 1)
15. Pattern/cloud appearing on agarose gel - (reply: 15)
16. TBE buffer-what is the role of each component? - (reply: 1)
17. Problems with having to run the gels for so long - (reply: 14)
18. Ethidium Bromide Agarose Gel Hazard - (reply: 6)
19. Single Plasmid Gel Band - (reply: 1)
20. Buffer in Gel - (reply: 6)
21. agarose gel electrophoresis - (reply: 5)
22. Uneven bands denaturing agarose - (reply: 2)
23. What gel percent and Voltage is needed to separate 2680bp and 2600bp DNA nicely - (reply: 7)
24. Smear on agarose gel from QIAGEN extracted plant samples - (reply: 1)
25. E gels and the E gel opener - (reply: 1)
26. Why do we use sponges in the Western Transfer? - (reply: 5)
27. Non-hazardous substitute for ethidium bromide? - (reply: 17)
28. What causes surface fluorescence on agarose gels? - (reply: 6)
29. Problems with PAGE gels - (reply: 1)
30. carpet in gels for PCR products - (reply: 2)