BBa_M45091BBa_M45091 Version 1 (Component)AGA1: Agglutinins, mating type specific cell surface Proteins, are synthesized by haploid cell of Sa
BBa_K242151BBa_K242151 Version 1 (Component)lacI promoter + lux I + TER + ptet-luxR-TER + lux pR - RFP
BBa_K1947023BBa_K1947023 Version 1 (Component)This part serves as a catch system expressed in <i>E. coli.
BBa_K547000BBa_K547000 Version 1 (Component)ready-to-inject backbone for T3SS, SlrP taged, with Bsa I cloning site
BBa_K802003BBa_K802003 Version 1 (Component)Shuttle vector for <i> E. coli</i> and <i>B. subtilis</i>
BBa_K1487073BBa_K1487073 Version 1 (Component)eYFP Reporter for tcpE gRNA target with strong promoter.
BBa_K1216014BBa_K1216014 Version 1 (Component)BBa_K1216014 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216012BBa_K1216012 Version 1 (Component)BBa_K1216012 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216013BBa_K1216013 Version 1 (Component)BBa_K1216013 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216011BBa_K1216011 Version 1 (Component)BBa_K1216007 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216010BBa_K1216010 Version 1 (Component)BBa_K1216010 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL. (
BBa_K223021BBa_K223021 Version 1 (Component)SoxS + Part:BBa_K152005 (Promoterless Synthetic Operon of CrtE,B,I,Y and GFP)
BBa_K1747012BBa_K1747012 Version 1 (Component)Fatty acid promoter - GFP - crt Z,E,B,I,Y - term - Repressor circuit
BBa_M11410BBa_M11410 Version 1 (Component)Type 2 promoter of sigE gene. Sigma factor regulates light and nitrogen responses, and has been obse
BBa_K1766008BBa_K1766008 Version 1 (Component)EnvZ_V5 osmoregulatory histidine kinase from <i>E.coli</i>.
BBa_K1766014BBa_K1766014 Version 1 (Component)EnvZ osmoregulatory histidine kinase from <i>E.coli.</i>
BBa_K2088006BBa_K2088006 Version 1 (Component)It encodes a kind of protein named 2Fe-2S ferredoxin, a 2Fe-2S iron-sulfur cluster binding domain. I
BBa_K187416BBa_K187416 Version 1 (Component)trpE in pAB
BBa_K809603BBa_K809603 Version 1 (Component)Bovine Pancreatic DNase I (in yeast mt codon table)
BBa_M11407BBa_M11407 Version 1 (Component)Type 1 promoter of hspA gene in Synechocystis sp. PCC 6803
BBa_M11408BBa_M11408 Version 1 (Component)Type 1 promoter of sigA gene in Synechocystis sp. PCC 6803
BBa_M11404BBa_M11404 Version 1 (Component)Type 1 promoter of psbA2 gene in Synechocystis sp. PCC 6803
BBa_M11411BBa_M11411 Version 1 (Component)Type 2 promoter of lrtA gene. Gene is expressed during darkness. Potentially darkness-induced promot
SEGASEGA_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.