Faculty of Science |
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N or C-terminal His tag. |
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pET28a-c
vector map
pET28a sequence pET28b sequence pET28c sequence |
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Parallel
vectors 1 & 3 contain N-terminal His (pET22), MBP (pMal) and GST (pGex)
with similar MCS for easy cloning.
Parallel vector 2 contains N and C-terminal His (pET22), MBP (pMal) and GST (pGex) with similar MCS for easy cloning. (The MCS is compatible to that of pFastBac for expression in insect cells) |
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pHis1, pHis2, pHis3 pGST1, pGST2, pGST3 pMBP1, pMBP2, pMBP3 |
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T7 promoter, N-term his tag followed by NusA fusion protein, another his-tag, S-tag, thrombin & enterkinase cleavage sites. HSV-tag and his-tags in the C-term are also available, provided a stop codon is not introduced. |
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(his tag [N,C] GST tag [N], MBP tag [N]) |
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pIVEX vectors were developed for in-vitro translation coupled with transcription by T7 polymerase (Roche RTS). Vectors containing N-term tags have a factor Xa cleavage site. The pIVEX vectors are not IPTG inducible and have a high copy origin. This may result in whole cells in constitutive protein expression which might harm the host cell. |
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1.
Gateway cloning technology - slides set
2. Invitrogen's Gateway main page 3. Gateway cloning technology - tutorial |
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Vector map +links to sequence |
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Vector map +links to sequence |
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N-terminal pelB signal sequence for potential periplasmic localization, plus optional C-terminal His tag. |
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pET22b
vector map
pET22b sequence |
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pET21a-d
vector map
pET21d sequence |
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Sumo3 Fusion Vector |
EMBL |
T7 promoter, his tag, TEV site, EGFP | Kan |
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Entries since October 2007
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