Welcome to
To date 11 ProteoCools are avallabile
Proteocool n° | Title | Page |
1 | Cloning methods overwiev | 1 |
2 | Primer Design: Restiction/Ligation | 1 |
3 | Primer Design: PIPE Cloning | 1 |
4 | PCR Colony screening | 1 |
5 | E.coli high cell density media overview | 2 |
6 | Rapid SDS-page coloration/decoloration using microwave | 3 |
7 | High cell density E.coli protein expression using EnpressoB media | 2 |
8 | Buffer Exchange methods overview | 3 |
9 | 2 Common mistakes causing sample lost using the AKTA Systems | 4 |
10 | PARAFILM a simple support for sample loading on agarose gel | 1 |
11 | Rapid buffer Exchange by PD-10 | 3 |
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