Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.

Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The Electro-regulated promoters are a collection of promoter responding to electrical signals in liquid media. These promoter were screened using the our High Throughput Electro Actuator (HTEA) Hardware and through the experiment described here.
Briefly, we use the HTEA to expose individaul clones of a library of 2000 E. coli promoter fused to Green Fluorescent protein. We mesure fold changes in the expression of the fluorescent protein between different shock conditions describe bellow:

• Condition B : Exposure to 1volt peak to peak AC Current, 100HZ for 2.5 seconds
• Condition C : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds
• Condition D : Exposure to 1volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours
• Condition E : Exposure to 3volt peak to peak AC Current, 100HZ for 20 seconds every 15 minutes for 2 hours

The figure on the left detail show the fold change fluorescence of the screened promoter compared to its control when exposed to specific electrical signals

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The pDuet_Bettencourt Vectors is a sets of 3 compatible vector for transformation in E. coli. We re-engineered the pETDuet System and cloned the Transcriptional unit of a GFP from the V35 vector of the CIDAR MoClo[1,2] flanked with BsaI restriction site and barcode A and E of the Moclo for assembly of entire transcriptional unit. Like so, during a Golden Gate Cloning, after the BsaI cut, the GFP is replaced by the insert. This allow for easy selection against Green fluorescence (compatible with the mScarlet reporter used in all of our toolkit)

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The pDuet_Bettencourt Vectors is a sets of 3 compatible vector for transformation in E. coli. We re-engineered the pETDuet System and cloned the Transcriptional unit of a GFP from the V35 vector of the CIDAR MoClo[1,2] flanked with BsaI restriction site and barcode A and E of the Moclo for assembly of entire transcriptional unit. Like so, during a Golden Gate Cloning, after the BsaI cut, the GFP is replaced by the insert. This allow for easy selection against Green fluorescence (compatible with the mScarlet reporter used in all of our toolkit)

References

Characterisation

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

The pDuet_Bettencourt Vectors is a sets of 3 compatible vector for transformation in E. coli. We re-engineered the pETDuet System and cloned the Transcriptional unit of a GFP from the V35 vector of the CIDAR MoClo[1,2] flanked with BsaI restriction site and barcode A and E of the Moclo for assembly of entire transcriptional unit. Like so, during a Golden Gate Cloning, after the BsaI cut, the GFP is replaced by the insert. This allow for easy selection against Green fluorescence (compatible with the mScarlet reporter used in all of our toolkit)

References

Characterisation | dpB.002

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.002 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pSoxS - dpB.002 experiment

References

Characterisation | dpB.003

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.003 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pSoxS - dpB.002 experiment

References

Characterisation | dpB.004

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.004 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pOxyS - dpB.004 experiment

References

Characterisation | dpB.005

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.005 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pOxyS - dpB.004 experiment

References

Characterisation | dpB.006

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.006 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pNasA - dpB.006 experiment

References

Characterisation | dpB.007

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.007 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pNasA - dpB.006 experiment

References

Characterisation | dpB.008

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.008 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

References

Characterisation | dpB.009

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.009 is an Input device that can transcribe an electrical signal into the production of a protein.
They are can be used to pass on signals to the Processors and downstream our signal processing pipeline.
They can also be used as standalone for prototyping and debug of for specific applications

References

Characterisation | dpB.010

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.010 is a Processor device that can receive signals from the Input device. CinR (transcription factor produced in the Input) activate pCin in the presence of OCH14 (its inducer). Signals can be transformed through already characterise synthetic biological components.
Processor devices pass on transformed signal downstream our signal processing pipeline and to the Output device.
They can also be used as standalone for prototyping and debug of for specific applications such as Bio-Sensing (See proposed implementation for exemples)

Characterisation is obtained from the dpB.010 experiment

References

Characterisation | dpB.011

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.011 is a Processor device that can receive signals from the Input device. CinR (transcription factor produced in the Input) activate pCin in the presence of OCH14 (its inducer). Signals can be transformed through already characterise synthetic biological components.
Processor devices pass on transformed signal downstream our signal processing pipeline and to the Output device.
They can also be used as standalone for prototyping and debug of for specific applications such as Bio-Sensing (See proposed implementation for exemples)

References

Characterisation | dpB.012

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.012 is a Processor device that can receive signals from the Input device. CinR (transcription factor produced in the Input) activate pCin in the presence of OCH14 (its inducer). Signals can be transformed through already characterise synthetic biological components.
Processor devices pass on transformed signal downstream our signal processing pipeline and to the Output device.
They can also be used as standalone for prototyping and debug of for specific applications such as Bio-Sensing (See proposed implementation for exemples)

References

Characterisation | dpB.013

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.013 is an Ouput device that can receive signals from the processor device. LuxRQ (transcription factor produced in the Processor) activate pLux78B in the presence of OC6 (its inducer). Signals are outputed as electronically readable information. (See Electrical resistance as a measure of OD)
They are can be used to report signals from computation upstream in our computation pipeline or as a standalone reporter
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the pLux76B - dpB.013 experiment

References

Characterisation | dpB.014

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.014 is an Ouput device that can receive signals from the processor device. LuxRQ (transcription factor produced in the Processor) activate pLux78B in the presence of OC6 (its inducer). Signals are outputed as electronically readable information. (See Electrical resistance as a measure of OD)
They are can be used to report signals from computation upstream in our computation pipeline or as a standalone reporter
They can also be used as standalone for prototyping and debug of for specific applications

Characterisation is obtained from the Lysis System - dpB.014 experiment

References

Characterisation | dpB.015

To visualize the interactive graph, click on the DATA button for each part of the collection.
Our plots are Interactive, hover your mouse to observe the data

Description

dpB.015 is an Ouput device that can receive signals from the processor device. LuxRQ (transcription factor produced in the Processor) activate pLux78B in the presence of OC6 (its inducer). Signals are outputed as electronically readable information. (See Electrical resistance as a measure of OD)
They are can be used to report signals from computation upstream in our computation pipeline or as a standalone reporter
They can also be used as standalone for prototyping and debug of for specific applications

See the LacZ page for info

References