|
1. Finding the mass of digested DNA by electrophoresis - (reply: 1)
2. Staining DNA and blotting - (reply: 1)
3. Why are my genotyping PCR bands blurry? - (reply: 4)
4. What casues dark zone in middle of DNA band on agarose gel? - (reply: 7)
5. Problems for DNA agarose gel visualization with a gel documentation system - (reply: 9)
6. Weird agarose melting at standard conditions - just at the wells?? - (reply: 1)
7. Faint band and primer dimer in PCR - (reply: 1)
8. Dye does not separe in acrylamide gel - (reply: 2)
9. 5X, 6X sds gel loading buffer - (reply: 4)
10. ethidium bromide contact - (reply: 1)
11. lower part of the gel was not stained - (reply: 7)
12. bands becoming wavy with colour of the dye changing to yellow - (reply: 1)
13. Fragment sizes smaller than expected - (reply: 1)
14. Electrophoresis problem: Frowning bands and smeary ladder - (reply: 1)
15. Agarose Gel consistency issues - (reply: 2)
16. very high salt concentration ?? - (reply: 4)
17. RNA electrophoresis - (reply: 2)
18. PCR product not migrating from wells...?? - (reply: 6)
19. How to determine gene knock-out from Agarose gel bands - (reply: 1)
20. An issue !! - (reply: 5)
21. What would be the adequate %gel/voltage/running time conditions for a ca. 320 kD - (reply: 3)
22. EMSA not detect a bindind - (reply: 7)
23. Visualization of DNA:RNA hybrid on TBE-UREA GEL - (reply: 8)
24. SDS page staning issue - (reply: 9)
25. All bands, including ladder, appear as double bands in EtBr stained gel - (reply: 6)
26. Forgot to wash the wells - (reply: 2)
27. Staining SDS-PAGE gel with EtBr? - (reply: 6)
28. DNA shows on Nanodrop but not on electrophoresis - (reply: 2)
29. Gel Bands - (reply: 1)
30. I want to separate two proteins having mw of 16.8 and 16.78 kDa. how can i accom - (reply: 2)
2. Staining DNA and blotting - (reply: 1)
3. Why are my genotyping PCR bands blurry? - (reply: 4)
4. What casues dark zone in middle of DNA band on agarose gel? - (reply: 7)
5. Problems for DNA agarose gel visualization with a gel documentation system - (reply: 9)
6. Weird agarose melting at standard conditions - just at the wells?? - (reply: 1)
7. Faint band and primer dimer in PCR - (reply: 1)
8. Dye does not separe in acrylamide gel - (reply: 2)
9. 5X, 6X sds gel loading buffer - (reply: 4)
10. ethidium bromide contact - (reply: 1)
11. lower part of the gel was not stained - (reply: 7)
12. bands becoming wavy with colour of the dye changing to yellow - (reply: 1)
13. Fragment sizes smaller than expected - (reply: 1)
14. Electrophoresis problem: Frowning bands and smeary ladder - (reply: 1)
15. Agarose Gel consistency issues - (reply: 2)
16. very high salt concentration ?? - (reply: 4)
17. RNA electrophoresis - (reply: 2)
18. PCR product not migrating from wells...?? - (reply: 6)
19. How to determine gene knock-out from Agarose gel bands - (reply: 1)
20. An issue !! - (reply: 5)
21. What would be the adequate %gel/voltage/running time conditions for a ca. 320 kD - (reply: 3)
22. EMSA not detect a bindind - (reply: 7)
23. Visualization of DNA:RNA hybrid on TBE-UREA GEL - (reply: 8)
24. SDS page staning issue - (reply: 9)
25. All bands, including ladder, appear as double bands in EtBr stained gel - (reply: 6)
26. Forgot to wash the wells - (reply: 2)
27. Staining SDS-PAGE gel with EtBr? - (reply: 6)
28. DNA shows on Nanodrop but not on electrophoresis - (reply: 2)
29. Gel Bands - (reply: 1)
30. I want to separate two proteins having mw of 16.8 and 16.78 kDa. how can i accom - (reply: 2)