BBa_K1456021
BBa_K1456021 Version 1 (Component)
Glutathione Peroxidase-1 (GPx-1) enzyme forward primer-2 with restriction site and kozak sequence

BBa_K1189020
BBa_K1189020 Version 1 (Component)
Light chain human ferritin with his-tag and E-coil under the lacI inducible promoter

BBa_K1179008
BBa_K1179008 Version 1 (Component)
A mutant DNA binding Cas9 with a C-terminal linker and BsaI site for ligation

BBa_K1456022
BBa_K1456022 Version 1 (Component)
Glutathione Peroxidase(GPx1) enzyme reverse primer-2 with restriction site, two stop codon and 6xHis

BBa_K1456024
BBa_K1456024 Version 1 (Component)
Human Tissue Plasminogen Activator reverse primer-2 with restriction site, 2 stop codons and 6XHis

BBa_K1189019
BBa_K1189019 Version 1 (Component)
Heavy chain human ferritin with his-tag and E-coil under the lacI inducible promoter

BBa_M1532
BBa_M1532 Version 1 (Component)
Thermal Hysteresis (Antifreeze) Protein (variant YL1) with 8-His tag with secretion tag and GFP

BBa_M1533
BBa_M1533 Version 1 (Component)
Thermal Hysteresis (Antifreeze) Protein (variant YL4) with 8-His tag with secretion tag and GFP

BBa_K079026
BBa_K079026 Version 1 (Component)
GFP reporter protein and LacI gene sequence under the control of J23118 constitutive promoter

BBa_K079024
BBa_K079024 Version 1 (Component)
LacI repressor under the control of the J23118 costitutive promoter and Lac 1 operator

BBa_K2116038
BBa_K2116038 Version 1 (Component)
AND gate103

BBa_I715069
BBa_I715069 Version 1 (Component)
Test part to see if RE and pLac +hixc can be expressed with GFP

BBa_K1657000
BBa_K1657000 Version 1 (Component)
It is called BAT. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid

BBa_M11051
BBa_M11051 Version 1 (Component)
Captures light energy and uses it to move protons across the membrane out of the cell.

BBa_K1172304
BBa_K1172304 Version 1 (Component)
Riboflavin synthesis gene cluster from s. oneidensis under control of T7 promoter and strong RBS

BBa_K1159309
BBa_K1159309 Version 1 (Component)
19 AA Linker with N-terminal <i>Strep</i>-tag II and C-terminal TEV cleavage site in RFC[25]

BBa_K1132037
BBa_K1132037 Version 1 (Component)
AND-inverted RFP gate (BBa_K1132034) with T7 polymerase under the control of a strong promoter

BBa_K1985014
BBa_K1985014 Version 1 (Component)
Sequence coding for Sup35(residues 1-61) and Cytochrome b562 with an arabinose inducible promoter

BBa_K1316009
BBa_K1316009 Version 1 (Component)
yqjF promoter coupled to mKate2 reporter gene and ybiJ promoter coupled to mKate2 reporter gene

BBa_K750008
BBa_K750008 Version 1 (Component)
Quorum sensing system based on LuxI and LuxR to control the expression of parts behind

pLacIQ+eGF
BBa_K193207 Version 1 (Component)
TmTHP with promotor for constituitive expression and with EGFP for fusion of Anti-Freeze Protein

T7+eGFP+Tm
BBa_K193208 Version 1 (Component)
TmTHP with promotor for constituitive expression and with EGFP for fusion of Anti-Freeze Protein

BBa_K774102
BBa_K774102 Version 1 (Component)
Multi sensor - for calculation of specific concentrations of nitrates nitrites and nitric oxide usin

BBa_K1412600
BBa_K1412600 Version 1 (Component)
Endow the CL-1(E.coli engineered strain) the ability of chemotaxis and quorum sensing

BBa_K1861020
BBa_K1861020 Version 1 (Component)
Fusion protein of the TALE constant domain and a SpyTag in an expression cassette

BBa_K325239
BBa_K325239 Version 1 (Component)
Red Firefly Luciferase and LRE (under pBAD)<BR><i>L. Cruciata<BR>(E. coli optimised)</i>

BBa_K594013
BBa_K594013 Version 1 (Component)
A device that can accepts the 3--O-C6-HSL and then produces 3-O-C12-HSL

BBa_M45760
BBa_M45760 Version 1 (Component)
K208010:M45710, A composite part for AvrA with a Lac promoter and ribosome binding site.

BBa_K539691
BBa_K539691 Version 1 (Component)
promoter(lacI regulated)+Alss+ilvC+ilvD(each preceded by own RBS)and RNA thermometer+terminator

BBa_K542012
BBa_K542012 Version 1 (Component)
Catechol 2,3-dioxygenase with a C-terminal Arg-tag and Double Terminator (no promoter/RBS)

BBa_K1647019
BBa_K1647019 Version 1 (Component)
Cap-AAP2, a improved antimicrobial peptide which can kill the S.mutans selectively and have changeab

BBa_K112223
BBa_K112223 Version 1 (Component)
{a~ihfB!} The ihf beta gene ready to have rbs attached and stop codon, BBb format

BBa_J54141
BBa_J54141 Version 1 (Component)
AND GATE"AHL and oleate"

BBa_K1657002
BBa_K1657002 Version 1 (Component)
It is called TAB. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid

BBa_K1657001
BBa_K1657001 Version 1 (Component)
It is called BAT. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid

BBa_K833014
BBa_K833014 Version 1 (Component)
constitutive promoter followed by a lox site with a bidirectional terminator and then a lox site.

BBa_K1657004
BBa_K1657004 Version 1 (Component)
It is called TAB. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid

BBa_K1657003
BBa_K1657003 Version 1 (Component)
It is called BAT. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid

SEGA
SEGA_collection Version 1 (Collection)
In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.

BBa_K880001
BBa_K880001 Version 1 (Component)
Asymmetrically digestible reporter to assay the activity of DNA recombinases FimE K137007 and HbiF K

BBa_K2176001
BBa_K2176001 Version 1 (Component)
Cassette for the constitutive production of GAL4-KaiCp and LexA-SasA, linked by a self-cleaving P2A

BBa_K1362061
BBa_K1362061 Version 1 (Component)
N-terminal chitin binding domain with triglycine linker and His-tag as RFC[105] insert

xis
BBa_K112204 Version 1 (Component)
{a~xis!} The bacteriophage lambda xis gene ready to have rbs attached and stop codon; assembly stand

BBa_K325109
BBa_K325109 Version 1 (Component)
EPIC Firefly Luciferase and LRE (under pBAD)<BR><i>P. Pyralis<BR>(E. coli optimised)</i>