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1. Can glucose-6-phosphate enter human cells? - (reply: 1)
2. Co-localisation Analysis - immunofluorescence - (reply: 5)
3. black spots are found in cells and medium - (reply: 1)
4. Cell Membranes as an active barrier - (reply: 1)
5. Normalise cell count for protein analysis - (reply: 3)
6. Blockage of cadherin bindings of MCF-10A cells without harming hydrogels and cal - (reply: 2)
7. Should Lineage marker cocktail be used in cell lines to remove lineage specific - (reply: 1)
8. When overexpressing several genes using different vectors, what negative control - (reply: 2)
9. Transfection - (reply: 2)
10. The true monomers making RNA and DNA ? - (reply: 1)
11. Co-transfection of multiple plasmids - (reply: 1)
12. Culturing LoVo cells - (reply: 1)
13. Luciferase assay - experimental design - (reply: 1)
14. Cytotoxicity of hoechst staining in overnight experiment - (reply: 1)
15. Lentivirus packaging (no fluorescence) - (reply: 1)
16. exosome isolation - (reply: 1)
17. Synchronization of HEK293T cells for IP - (reply: 2)
18. About closing a Class II safety cabinet - (reply: 2)
19. Cell volume and reciprocal cell volume? Whaaat? - (reply: 1)
20. The adipose cell culturing - (reply: 2)
21. Migration Inhibitors - (reply: 1)
22. E-Cadherin Expression in OAW-42 Cells - (reply: 1)
23. Why HepG2 cells looked like that? - (reply: 2)
24. Cell death determination - (reply: 2)
25. Does anyone know of a stict S phase marker? - (reply: 2)
26. Jurkat cell - normal receptor/gene expressivity - (reply: 1)
27. GFP+ Transf. HEK293 GFP- in fluorescence microscopy? - (reply: 1)
28. Viral-Exososme Neutralization - (reply: 2)
29. control shRNA - (reply: 2)
30. Is any other method to maintain without changing media, or store cell culture fo - (reply: 2)
2. Co-localisation Analysis - immunofluorescence - (reply: 5)
3. black spots are found in cells and medium - (reply: 1)
4. Cell Membranes as an active barrier - (reply: 1)
5. Normalise cell count for protein analysis - (reply: 3)
6. Blockage of cadherin bindings of MCF-10A cells without harming hydrogels and cal - (reply: 2)
7. Should Lineage marker cocktail be used in cell lines to remove lineage specific - (reply: 1)
8. When overexpressing several genes using different vectors, what negative control - (reply: 2)
9. Transfection - (reply: 2)
10. The true monomers making RNA and DNA ? - (reply: 1)
11. Co-transfection of multiple plasmids - (reply: 1)
12. Culturing LoVo cells - (reply: 1)
13. Luciferase assay - experimental design - (reply: 1)
14. Cytotoxicity of hoechst staining in overnight experiment - (reply: 1)
15. Lentivirus packaging (no fluorescence) - (reply: 1)
16. exosome isolation - (reply: 1)
17. Synchronization of HEK293T cells for IP - (reply: 2)
18. About closing a Class II safety cabinet - (reply: 2)
19. Cell volume and reciprocal cell volume? Whaaat? - (reply: 1)
20. The adipose cell culturing - (reply: 2)
21. Migration Inhibitors - (reply: 1)
22. E-Cadherin Expression in OAW-42 Cells - (reply: 1)
23. Why HepG2 cells looked like that? - (reply: 2)
24. Cell death determination - (reply: 2)
25. Does anyone know of a stict S phase marker? - (reply: 2)
26. Jurkat cell - normal receptor/gene expressivity - (reply: 1)
27. GFP+ Transf. HEK293 GFP- in fluorescence microscopy? - (reply: 1)
28. Viral-Exososme Neutralization - (reply: 2)
29. control shRNA - (reply: 2)
30. Is any other method to maintain without changing media, or store cell culture fo - (reply: 2)