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Found 1 matching solution for this experiment
pET32(a)+-BLS
R., Sekhavati, Department of Animal Science, Faculty of Agricult
Upstream tips |
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The BLS fragments sub-cloned in pET32 (a) + vector (Novagen, USA), and subsequently was transformed into E.coli BL21 (DE3) expression host strain (Novagen, USA). The harboring transformed bacteria was spread on LB agar containing 50 µg/mL ampicillin (Sigma, Germany) cultivation and incubated at 37 °C overnight. |
To analyze the expression of recombinant BLS both the supernatant and the pellet were evaluated on SDS-PAGE 10% (upper gel was 8% and lower gel was 10%). |
Protocol tips |
The BLS fragments sub-cloned in pET32 (a) + vector (Novagen, USA), and subsequently was transformed into E.coli BL21 (DE3) expression host strain (Novagen, USA). The harboring transformed bacteria was spread on LB agar containing 50 µg/mL ampicillin (Sigma, Germany) cultivation and incubated at 37 °C overnight. |
Downstream tips |
To analyze the expression of recombinant BLS both the supernatant and the pellet were evaluated on SDS-PAGE 10% (upper gel was 8% and lower gel was 10%). |
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