|
Top :
New Forum Archives (2009-): :
1. Antibiotic not working in LB agar, fine in broth - (reply: 3)
3. Generating a cell line using sleeping beauty transposase and a gene that contain - (reply: 1)
5. Trouble transforming pET28a in E. coli BL21(DE3) - (reply: 5)
7. Designing Crispr guides and cloning into appropriate vectors - (reply: 1)
9. Cloning protein of interest into lentiviral vector - help - I have no experience - (reply: 20)
11. PCRed-vector approach to tag switching - (reply: 1)
13. Blunt-end ligation: what if the vector and insert are both phosphorylated? - (reply: 4)
15. Neomycin/Kanamycin Resistant gene - (reply: 2)
17. Why do I get two bands on the gel of a digested PCR product after purification w - (reply: 1)
19. Transformation - (reply: 3)
21. Ligate a very small insert into a vector - (reply: 3)
23. Plasmid dna size - (reply: 3)
25. Express two different membrane proteins on the same promoter - (reply: 1)
27. [Overexpression] Without upstream transcription terminator - (reply: 4)
29. Ampicillin LB agar reheating and reusing - (reply: 2)
3. Generating a cell line using sleeping beauty transposase and a gene that contain - (reply: 1)
5. Trouble transforming pET28a in E. coli BL21(DE3) - (reply: 5)
7. Designing Crispr guides and cloning into appropriate vectors - (reply: 1)
9. Cloning protein of interest into lentiviral vector - help - I have no experience - (reply: 20)
11. PCRed-vector approach to tag switching - (reply: 1)
13. Blunt-end ligation: what if the vector and insert are both phosphorylated? - (reply: 4)
15. Neomycin/Kanamycin Resistant gene - (reply: 2)
17. Why do I get two bands on the gel of a digested PCR product after purification w - (reply: 1)
19. Transformation - (reply: 3)
21. Ligate a very small insert into a vector - (reply: 3)
23. Plasmid dna size - (reply: 3)
25. Express two different membrane proteins on the same promoter - (reply: 1)
27. [Overexpression] Without upstream transcription terminator - (reply: 4)
29. Ampicillin LB agar reheating and reusing - (reply: 2)