Team:NRP-UEA-Norwich/Project Parts

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Revision as of 12:59, 15 October 2014

NRP UEA Norwich iGEM 2014

Parts

New Parts


Bax (Bba_K1467203)
A reporter gene which, when transcribed, produces Bax protein that has a role in positively regulating cell apoptosis. The part has been made compatible with the GoldenGate MoClo Assembly Standard by removal of internal BsaI and BpiI recognition sequences.

Improved parts


RFP coding device - Golden Gate Module Flipper (Bba_K1467100)
A "GoldenGate Flipper" that can be used to convert Pro + 5U (promoter and 5' untranslated leader) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.

RFP coding device - Golden Gate Module Flipper (Bba_K1467200)
A "GoldenGate Flipper" that can be used to convert CDS1 modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.

RFP coding device - Golden Gate Module Flipper (Bba_K1467300)
A "GoldenGate Flipper" that can be used to convert 3U + Ter (3' untranslated region and terminator) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.

RFP coding device - Golden Gate Module Flipper (Bba_K1467400)
This part is a "GoldenGate Flipper" that can be used to assemble complete transcriptional units from GoldenGate MoClo Standard Parts producing a standard BioBrick. It consists of the RFP reporter (from BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.

AmilCP (Bba_K1467201)
A reporter chromoprotein which produces strong blue colour when expressed. A variation of the part BBa_K592009 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard and RFC 105.

AmilGFP (Bba_K1467202)
A reporter chromoprotein which produces strong yellow colour when expressed. A variation of the part BBa_K592010 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard and RFC 105.

GFP (Bba_K1467204)
A reporter protein that produces green fluorescence under UV light when expressed. A variation of the part BBa_E0040 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard and RFC 105.

Plant specific parts


Mannopine synthase (MAS) Promoter (Bba_K1467104)
A plant specific constitute promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites.

BS3 Promoter (Bba_K1467102)
A plant specific, TALE inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of the TALE AvrBS3, driving the expression of coding regions.

PDF1.2 Promoter (Bba_K1467103)
A plant specific, Methyl Jasmonate inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of methyl jasmonate (high methyl jasmonate levels indicate plant stress, often as a result of pathogen infection), driving the expression of coding regions.

35s Promoter (Bba_K1467101)
A plant specific constitutive promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The part was originally obtained from the Cauliflower Mosaic Virus and is intended for use as a constitutive promoter for gene expression experiments in plants.

AvrBS3 TALE (Bba_K1467205)
TAL (transcription activator-like) Effector that induces the BS3 promoter allowing safe testing of pathogen induced systems in the laboratory. The part has been made compatible with the GoldenGate MoClo Assembly Standard by removal of internal BsaI and BpiI recognition sequences.

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