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Top : New Forum Archives (2009-): : Electrophoresis
1. Weird agarose melting at standard conditions - just at the wells?? - (reply: 1)
2. Faint band and primer dimer in PCR - (reply: 1)
3. Dye does not separe in acrylamide gel - (reply: 2)
4. 5X, 6X sds gel loading buffer - (reply: 4)
5. ethidium bromide contact - (reply: 1)
6. lower part of the gel was not stained - (reply: 7)
7. bands becoming wavy with colour of the dye changing to yellow - (reply: 1)
8. Fragment sizes smaller than expected - (reply: 1)
9. Electrophoresis problem: Frowning bands and smeary ladder - (reply: 1)
10. Agarose Gel consistency issues - (reply: 2)
11. very high salt concentration ?? - (reply: 4)
12. RNA electrophoresis - (reply: 2)
13. PCR product not migrating from wells...?? - (reply: 6)
14. How to determine gene knock-out from Agarose gel bands - (reply: 1)
15. An issue !! - (reply: 5)
16. What would be the adequate %gel/voltage/running time conditions for a ca. 320 kD - (reply: 3)
17. EMSA not detect a bindind - (reply: 7)
18. Visualization of DNA:RNA hybrid on TBE-UREA GEL - (reply: 8)
19. SDS page staning issue - (reply: 9)
20. All bands, including ladder, appear as double bands in EtBr stained gel - (reply: 6)
21. Forgot to wash the wells - (reply: 2)
22. Staining SDS-PAGE gel with EtBr? - (reply: 6)
23. DNA shows on Nanodrop but not on electrophoresis - (reply: 2)
24. Gel Bands - (reply: 1)
25. I want to separate two proteins having mw of 16.8 and 16.78 kDa. how can i accom - (reply: 2)
26. Sequencing gels equipment query - (reply: 2)
27. Electrophoresis Imaging - (reply: 1)
28. Electrophoresis after PCR : too many bands - (reply: 6)
29. Homogenous Cell Lysates - (reply: 1)
30. SDS PAGE sample prep - (reply: 3)

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