Team:Warsaw/Calendar-Main/1 August 2008

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<img src="https://static.igem.org/mediawiki/2008/7/7c/Cos.jpg" width=300/> <var><b>Fig. 1. Colony PCR to find proper clones of pACYC177_OmpA_alpha+deltaA and pACYC177_OmpA_omega+deltaA</b><br>  
<img src="https://static.igem.org/mediawiki/2008/7/7c/Cos.jpg" width=300/> <var><b>Fig. 1. Colony PCR to find proper clones of pACYC177_OmpA_alpha+deltaA and pACYC177_OmpA_omega+deltaA</b><br>  
Upper gel:<br>
Upper gel:<br>

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Cloning of truncated fragment of protein A

Michał K.

  1. Colony PCR on pACYC177+OmpA_alpha + ΔA and pACYC177+OmpA_omega + ΔA colonies of tranformants.
  2. Gel electrophoresis of PCR products (Fig. 1.).

Fig. 1. Colony PCR to find proper clones of pACYC177_OmpA_alpha+deltaA and pACYC177_OmpA_omega+deltaA
Upper gel:
1. Marker
2-13. colony PCR products to find proper clone of pACYC177_OmpA_alpha+deltaA
Lower gel:
1. Marker
2-11. colony PCR products to find proper clone of pACYC177_OmpA_omega+deltaA
12. positive control - pACYC_OmpA_A_alpha
13. negative control - pACYC_OmpA_Z_alpha



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