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Team:Shenzhen SZMS

Team:Shenzhen SZMS

From 2013hs.igem.org . So the goal of our project is to provide an efficient and a more environment friendly method of detecting nitrates/nitrites and we strive to design biosensors to avoid the disadvantages of traditional methods. Our team is going to develop novel modular biosensors that enable cost-effective and on-site detection of .

Team:Chalmers-Gothenburg/Project

Team:Chalmers-Gothenburg/Project

Project. Contaminations – a problem you definitely want to get rid of as quickly as possible. It can destroy your product and lower the efficiency of the process, which in the end may lead to higher expenses. We have created a great system for both finding and combating contaminations in bioreactors.

Team:UrbanTundra Edmonton/Experimental

Team:UrbanTundra Edmonton/Experimental

The solution we settled upon was a modular multistage bioreactor. The bioreactor would consist of five main stages, each of each of which would be responsible for a separate task in the bioremediation process. The bioreactor would initially begin the extraction process with the introduction of the perchlorate rich soil into water.

Team:Toronto/Technology-Applications

Team:Toronto/Technology-Applications

Bioreactor Design. The goal of our project is to sunthesize bacteria that can effectively degrade Toluene. At the same time we are aware of the safety concerns and public perception of introduction of synthetic organisms into the environment.

Team:IISc Bangalore/Description

Team:IISc Bangalore/Description

As stated in the introduction, our project is an attempt to modify E coli to lower capital and running costs for rDNA bioreactor systems, by automating protein over-expression induction and separation of cell from growth media. . We acknowledge previous iGEM teams who have worked on Ag43 (Hokkaido University, 2012; Aberdeen Scotland, 2014 and .

Team:Toronto/Model

Team:Toronto/Model

Introduction The goal of the 2018 iGEM team was to explore an alternative waste-water cleaning mechanism that is both environmentally friendly and economically feasible. We hypothesized that one could genetically engineer E. coli to bind to waste particles, and then float to the surface of the reactor, allowing for easy E. coli removal.

Team:Wash U/Project

Team:Wash U/Project

Introduction. Our project goal is to maximize the photosynthetic productivity of a series of photobioreactors containing Rhodobacter sphaeroides under both high and low light intensities by synthetically regulating the size of the light-harvesting antenna complex LH2. We chose to undertake such a project using R. sphaeroides due to its well-characterized photosynthetic and genetic system.

Team:NYMU-Taipei/HP/Gold Integrated

Team:NYMU-Taipei/HP/Gold Integrated

After the 5th Asia-Pacific iGEM Conference, NYMU team had a chance to contact the primary instructor of NTHU team, Dr. Ya-Tang Yang, and his laboratory students. Dr. Yang is the associate professor of Institute of Electronics Engineering, National Tsing Hua University.They provided us with a set of Photo-Bioreactor made by themselves and taught .

Competition/Tracks/Hardware

Competition/Tracks/Hardware

Traditional hardware for synthetic biology tend to be expensive and complicated machines, creating a barrier to entry for many would-be innovators. iGEM teams in the past have met this challenge and built hardware that is affordable, easy to make, and open. Bioreactors. Engineered organisms typically require culturing in an in vitro environment.

iGEM in space: a Q&A with the Brown-Stanford team .

iGEM in space: a Q&A with the Brown-Stanford team .

May 24, 2012 · The Brown-Stanford iGEM team literally had the opportunity to do research which was, as described at the iGEM championship, "out of this world." Your projects tackle many different challenges .

Team:Calgary/Project/OSCAR/CatecholDegradation

Team:Calgary/Project/OSCAR/CatecholDegradation

This assay was completed by following the protocol written by the 2008 Edinburgh iGEM team. Figure 3: Results of the catechol visual assay using xylE BBa_K118021 . Cultures were grown overnight in LB and the pellets were washed with M9-MM at various times (From left .

Team:Humboldt Berlin/Hardware

Team:Humboldt Berlin/Hardware

So it was important to us, that every iGEM team who wants to continue our project,or any new project using a phototrophic organism, has a low-price but efficient way to fulfill their great ideas. For only 588 € it is possible to rebuild our bioreactor that offers many opportunities to design a set-up tailored to the needs of innovative projects.

Team:Tianjin/Project/Introduction

Team:Tianjin/Project/Introduction

(From TJU iGEM Team 2013) However, it is a long way to engineer a microorganism to produce alkanes and to optimize its productivity to satisfy the needs of industrial process. For researchers, it is important to detect and measure the concentration of alkanes, especially real time concentration of alkanes in vivo .

Team:Imperial College/MSDS

Team:Imperial College/MSDS

Safety forms were approved on October 2nd, 2013 by the iGEM Safety Committee. 1. Do the biological materials used in the lab work pose any risks to the safety and health of team members or others working in the lab? In the project, we used Escherichia. coli K-12 strains MG1655, NEB 10 beta, NEB 5 alpha and 0 (similar to E. coli K-12 DH 10 beta.

Team:UrbanTundra Edmonton/Experimental

Team:UrbanTundra Edmonton/Experimental

The solution we settled upon was a modular multistage bioreactor. The bioreactor would consist of five main stages, each of each of which would be responsible for a separate task in the bioremediation process. The bioreactor would initially begin the extraction process with the introduction of the perchlorate rich soil into water.

Team:Sheffield/modelling

Team:Sheffield/modelling

Introduction As a team we were adamant that the end goal of our project was not only to develop a novel biological process and demonstrate its success, but to design a product with potential for application in the real world. . The perfusion Bioreactor consists of a bioreactor which has two perforated 316L SS plates that house a bed of .

Team:Shenzhen SZMS

Team:Shenzhen SZMS

From 2013hs.igem.org . So the goal of our project is to provide an efficient and a more environment friendly method of detecting nitrates/nitrites and we strive to design biosensors to avoid the disadvantages of traditional methods. Our team is going to develop novel modular biosensors that enable cost-effective and on-site detection of .

Competition/Tracks/Hardware

Competition/Tracks/Hardware

Traditional hardware for synthetic biology tend to be expensive and complicated machines, creating a barrier to entry for many would-be innovators. iGEM teams in the past have met this challenge and built hardware that is affordable, easy to make, and open. Bioreactors. Engineered organisms typically require culturing in an in vitro environment.

CRISPR

CRISPR

Introduction to CRISPR and Cas9. From UBC 2013: CRISPRs (Clustered Regularly Interspaced Short PalindromicRepeats) are specific regions in some bacterial and archaeal genomes that, together with associated Cas (CRISPR-associated) genes, function as an adaptive immune system in prokaryotes.While the specific 'adaptive' nature of this immunity is still under .

Team:WHU-China/Introduction

Team:WHU-China/Introduction

[1] Jugder B-E, Ertan H, Bohl S, Lee M, Marquis CP and Manefield M (2016) Organohalide Respiring Bacteria and Reductive Dehalogenases: Key Tools in Organohalide Bioremediation.Front. Microbiol. 7:249. doi: 10.3389/fmicb.2016.00249 [2] Karl AP Payne, Carolina P Quezada Reductive dehalogenase structure suggests a mechanism for B12-dependent dehalogenation Nature 2015 January 22; .

Team:Warsaw/Project

Team:Warsaw/Project

The pmrA/pmrB system, which our team used in the project, also belongs to this class. pmrB is a histidine kinase and pmrA is a response regulator which strongly enhances expression upon binding to Pmr C. In order to understand better the mechanism of the system and to prevent any problems before starting the experiments in the wetlab we decided .

Team:Toronto/Safety

Team:Toronto/Safety

The iGEM Toronto 2015 wet lab team was composed of 4 wet lab team leads, 3 lab managers and 15 general members. Due to the size and sensitivity of our project,following proper safety protocols was paramount. This was achieved by establishing safety controls at .

Team:Aachen/Hardware

Team:Aachen/Hardware

Introduction & Motivation. . which is too expensive if we want other teams to pick up on our project. The iGEM-team from Aachen of 2015 already built Do-It-Yourself peristaltic pumps based on a design from thingiverse. [4] . The pumps of the 2015 team were designed for continuous pumping in a bioreactor, where they did a great job, but they .

Team:Tokyo-NoKoGen/bmc

Team:Tokyo-NoKoGen/bmc

Team. Members. Project: EcoLion. BioBricks. Notebook. Protocols. Attribution. Safety. Sponsors. BMC (Bacterial micro compartment) – localizing target proteins into BMC . 1. Introduction. For our project EcoLion, we came up with an idea to localize and concentrate heavy metals captured by metallothioneins into a "bacterial micro compartment".

Team:Wash U/Biological Parts

Team:Wash U/Biological Parts

The puc promoterpromotes transcription of the LH2 pucB/A genes naturally in Rhodobacter sphaeroides.It is important that we are able to compare the transcription rate of the puc promoter in the natural system vs. our mutant system so that we can determine exactly how much efficiency is gained by adding a red light sensor.

Team:TU Kaiserslautern/Attributions

Team:TU Kaiserslautern/Attributions

Realizing a great project idea does not only take compassion but also committed people forming a team together. Without the help of all the people we attribute to our project wouldn't have gone this far. Thanks to everyone – for small favors, lending an ear, steady care and everything that has been done for us!

iGEM - CMD Moodle

iGEM - CMD Moodle

This team also won a gold medal. Past iGEM teams fromAmsterdam iCE. coli The Amsterdam team first competed in iGEM in 2011 with the project icE. coli. Their goal was to optimize E. coli growth at colder temperatures and survive freezing environments. This year, the VU University hosted the first European regional Jamboree, where the Amsterdam .

Team:Exeter/Design

Team:Exeter/Design

In DPRB, Cld, PcrA, and PcrC are transported to the periplasm using unique signal peptides and the bacteria's TAT transport system. We wanted to harness the E. coli TAT system, so we had to confirm that the signal pepides would interact wi the E. coli TAT system in the same way. We did this by attaching GFP to these signal peptides, self fractionating the cell and then performing a Western .

Team:TU Dresden/Project/Description

Team:TU Dresden/Project/Description

Description. Introduction. Our project is called SPACE-P (Structural Phage Assisted Continuous Evolution of Proteins) and is part of the Synthetic Biology field. It focuses on accelerating the process of developing protein binding partners, which is required in pharmaceutical research as well as biotechnology and many other fields of science.

Team:WHU-China/Introduction

Team:WHU-China/Introduction

[1] Jugder B-E, Ertan H, Bohl S, Lee M, Marquis CP and Manefield M (2016) Organohalide Respiring Bacteria and Reductive Dehalogenases: Key Tools in Organohalide Bioremediation.Front. Microbiol. 7:249. doi: 10.3389/fmicb.2016.00249 [2] Karl AP Payne, Carolina P Quezada Reductive dehalogenase structure suggests a mechanism for B12-dependent dehalogenation Nature 2015 January 22; .