Team:Bielefeld-Germany/Project/Background/Technology

From 2011.igem.org

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[[File:Bielefeld-Germany-2011-PCR1.png|200px|thumb|right|One of our PCR devices]]
[[File:Bielefeld-Germany-2011-PCR1.png|200px|thumb|right|One of our PCR devices]]
-
[[File:Bielefeld-Germany2011-PCR3.png|200px|thumb|right|Our Real-time PCR device]]
+
[[File:Bielefeld-Germany2011-PCR3.png|200px|thumb|right|Our real-time PCR device]]
-
The polymerase chain reaction (PCR) is a method to reproduce DNA in vitro. An enzyme, the polymerase, is used for this purpose. The term "chain reaction" in this context means the fact, that the products of previous cycles are used as template for the next cycle and thus exponential amplification of specific DNA fragments is achieved. The formed DNA product results from defined primers, which are the start point for the polymerase.
+
The polymerase chain reaction (PCR) is a method to reproduce DNA in vitro. An enzyme, the polymerase, is used for this purpose. The term "chain reaction" in this context means, that the products of previous cycles are used as template for the next cycle and thus exponential amplification of specific DNA fragments is achieved. The formed DNA product results from defined primers, which are the start point for the polymerase.
-
The PCR is used in biological and medical laboratories for a variety of different tasks. In our case we used the PCR for two different applications.  It is possible to check successful cloning when using primers that bind at the prefix and suffix regions of the cloning plasmid and separate/analyze the PCR product by agarose gel electrophoresis (Colony PCR). The other application is the amplification and cloning of genomic DNA. We further used our thermocyclers for the qualification of our molecular beacons. A thermal profile was taken by meassuring the fluorescence of the beacons as a function of temperature by a Real-time PCR device.
+
The PCR is used in biological and medical laboratories for a variety of different tasks. In our case we used the PCR for two different applications.  It is possible to check successful cloning when using primers that bind at the prefix and suffix regions of the cloning plasmid and separate/analyze the PCR product by agarose gel electrophoresis (Colony PCR). The other application is the amplification and cloning of genomic DNA. We further used our thermocyclers for the qualification of our molecular beacons. A thermal profile was taken by measuring the fluorescence of the [[Team:Bielefeld-Germany/Project/Background/NAD#Applications_of_molecular_beacons|molecular beacons]] as a function of temperature by a real-time PCR device.
-
For the Colony PCR we used the [http://www.biometra.com/thermocycler-silver.0.html TProfessional Thermocycler] by Biometra and the [http://www.analytik-jena.com/en/LifeScience-AnalytikJenaAG/Products-/Instruments/Thermal-cycler__2266/ FlexCycler] by analytikjena. The thermal profile assay was performed with the [http://www.roche-applied-science.com/sis/rtpcr/htc/index.jsp LightCycler<html>&reg;</html> 480 System] by Roche.
+
For the colony PCR we used the [http://www.biometra.com/thermocycler-silver.0.html TProfessional Thermocycler] by Biometra and the [http://www.analytik-jena.com/en/LifeScience-AnalytikJenaAG/Products-/Instruments/Thermal-cycler__2266/ FlexCycler] by Analytik Jena. The thermal profile assay was performed with the [http://www.roche-applied-science.com/sis/rtpcr/htc/index.jsp LightCycler<html>&reg;</html> 480 System] by Roche.
Line 17: Line 17:
<partinfo>K525002</partinfo>;
<partinfo>K525002</partinfo>;
<partinfo>K525005</partinfo>;
<partinfo>K525005</partinfo>;
 +
<partinfo>K525006</partinfo>;
<partinfo>K525007</partinfo>;
<partinfo>K525007</partinfo>;
<partinfo>K525008</partinfo>;
<partinfo>K525008</partinfo>;
 +
<partinfo>K525009</partinfo>;
 +
<partinfo>K525010</partinfo>;
<partinfo>K525121</partinfo>;
<partinfo>K525121</partinfo>;
<partinfo>K525123</partinfo>;
<partinfo>K525123</partinfo>;
Line 25: Line 28:
<partinfo>K525223</partinfo>;
<partinfo>K525223</partinfo>;
<partinfo>K525224</partinfo>;
<partinfo>K525224</partinfo>;
 +
<partinfo>K525234</partinfo>;
<partinfo>K525301</partinfo>;
<partinfo>K525301</partinfo>;
<partinfo>K525303</partinfo>;
<partinfo>K525303</partinfo>;
Line 45: Line 49:
<partinfo>K525551</partinfo>;
<partinfo>K525551</partinfo>;
<partinfo>K525560</partinfo>;
<partinfo>K525560</partinfo>;
 +
<partinfo>K525562</partinfo>;
 +
<partinfo>K525582</partinfo>;
<partinfo>K525710</partinfo>;
<partinfo>K525710</partinfo>;
<partinfo>K525720</partinfo>;
<partinfo>K525720</partinfo>;
Line 56: Line 62:
==HPLC==
==HPLC==
-
High performance liquid chromatography (HPLC), a sort of liquid chromatography, is an analytical method in chemistry, not only to separates substances, but also to identify and quantify these substances by internal standards.
+
High performance liquid chromatography (HPLC), a sort of liquid chromatography, is an analytical method in chemistry, not only to separate substances, but also to identify and quantify these substances using internal standards.
[[File:Bielefeld-Germany2011-HPLC.png|200px|thumb|right|Our HPLC device]]
[[File:Bielefeld-Germany2011-HPLC.png|200px|thumb|right|Our HPLC device]]
-
The examined substance, together with a mobile phase, is pumped through a separation column that contains the stationary phase. You can classify an HPLC according to the principle of separation in normal phase (NP), reverse phase (RP), ion exchange (IEC), size exclusion (SEC) and chiral chromatography.
+
The examined substance, together with a mobile phase, is pumped through a separation column, the stationary phase. You can classify an HPLC according to the principle of separation in normal phase (NP), reverse phase (RP), ion exchange (IEC), size exclusion (SEC) and chiral chromatography.
-
The substance to be tested is injected into the stream of the mobile phase in small amounts. The movement of the probe trough the column depends on the natures of the sample on the one hand and the stationary phase on the other hand. If one component of the tested substance interacts strongly with the stationary phase, it remains on the column relatively long. If the interaction of a substance is weak, its velocity to leave the column is higher. The time at which a specific substance elutes is called retention time and is suitable for identification under particular conditions.
+
The substance to be tested is injected into the stream of the mobile phase in small amounts. The movement of the sample through the column depends on the nature of the sample on the one hand and the stationary phase on the other hand. If one component of the tested substance interacts strongly with the stationary phase, it remains on the column relatively long. If the interaction of a substance is weak, its velocity to leave the column is higher. The time at which a specific substance elutes is called retention time and is suitable for identification under particular conditions.
You can find the specifications of our HPLC device [https://2011.igem.org/Team:Bielefeld-Germany/Protocols/Analytics#HPLC_method here].
You can find the specifications of our HPLC device [https://2011.igem.org/Team:Bielefeld-Germany/Protocols/Analytics#HPLC_method here].
-
We used the HPLC to characterize the following BioBricks:  
+
We used the HPLC to characterize the following BioBricks:
 +
<partinfo>K525311</partinfo>;
<partinfo>K525512</partinfo>;
<partinfo>K525512</partinfo>;
<partinfo>K525515</partinfo>;
<partinfo>K525515</partinfo>;
-
<partinfo>K525517</partinfo>
+
<partinfo>K525517</partinfo>;
 +
<partinfo>K525551</partinfo>;
 +
<partinfo>K525560</partinfo>;
 +
<partinfo>K525562</partinfo>;
 +
<partinfo>K525582</partinfo>
<br style="clear: both" />
<br style="clear: both" />
Line 74: Line 85:
==MS/MS==
==MS/MS==
-
Tandem mass spectrometry (MS/MS) is an analytical physics technique with multiple mass spectrometry sections combined. Between two analyzers, a collision cell is mounted to apply energy to the ions by colliding with an inert gas (usually nitrogen or argon). Thereafter the ions disintegrate very specific to other, lighter ions.
+
Tandem mass spectrometry (MS/MS) is an analytical physics technique with multiple mass spectrometry sections combined. Between two analyzers, a collision cell is mounted to apply energy to the ions by colliding them with an inert gas (usually nitrogen or argon). Thereafter the ions disintegrate very specific to other, lighter ions.
<br style="clear: both" />
<br style="clear: both" />
Line 98: Line 109:
[[File:Bielefeld-Germany2011-MALDI-TOF.png|200px|thumb|right|Our MALDI-TOF device]]
[[File:Bielefeld-Germany2011-MALDI-TOF.png|200px|thumb|right|Our MALDI-TOF device]]
-
Before measuring, the analyte is cocristalized on an metal plate within a solid matrix, 3,5-dimethoxy-4-hydroxycinnamic acid (sinapinic acid) and 2,5-dihydroxybenzoic acid (DHB) are most commonly used.
+
Before measurement, the analyte is co-crystallized on a metal plate within a solid matrix. 3,5-dimethoxy-4-hydroxycinnamic acid (sinapinic acid) and 2,5-dihydroxybenzoic acid (DHB) are most commonly used.
-
Desorption of the analyte is taken by a laser beam, commonly with a wavelength of 337 nm. The matrix absorbs the laser light and the upper layer explosively vaporizes, ejecting both, matrix and analyte molecules. In addition to this vaporization, the laser beam also leads to an ionization of the analytes. The mass analysis is taken by the TOF (Time of flight)-Analysator. The evaporated ions are accelerated by an electric field. Typical acceleration voltages for this are 10-30 kV. The velocity of an ion depends on his mass and the charge. An ion detector converts the incoming ions into an electrical signal. The advantage of this method is the rapid analysis of a relatively large mass range.
+
Desorption of the analyte is taken by a laser beam, commonly with a wavelength of 337 nm. The matrix absorbs the laser light and the upper layer explosively vaporizes, ejecting both, matrix and analyte molecules. In addition to this vaporization, the laser beam also leads to an ionization of the analytes. The mass analysis is performed by the TOF (time of flight)-analysator. The evaporated ions are accelerated in an electric field. Typical acceleration voltages for this are 10-30 kV. The velocity of an ion depends on its mass and the charge. An ion detector converts the incoming ions into an electrical signal. The advantage of this method is the rapid analysis of a relatively large mass range.
The MALDI-TOF analysis was performed with the [http://www.bdal.com/products/maldi/ultraflextreme-series/overview.html ultrafleXtreme<html>&#8482;</html>] by Bruker Daltonics.
The MALDI-TOF analysis was performed with the [http://www.bdal.com/products/maldi/ultraflextreme-series/overview.html ultrafleXtreme<html>&#8482;</html>] by Bruker Daltonics.
Line 111: Line 122:
<partinfo>K525223</partinfo>;
<partinfo>K525223</partinfo>;
<partinfo>K525224</partinfo>;
<partinfo>K525224</partinfo>;
 +
<partinfo>K525710</partinfo>
Line 117: Line 129:
==Fluorescence Assay==
==Fluorescence Assay==
-
[[File:Bielefeld-Germany-2011-Tecan.png|200px|thumb|right|Our fluorescence assay device]]
+
[[File:Bielefeld-Germany-2011-Tecan.png|200px|thumb|right|One of our fluorescence assay devices]]
-
The fluorescence assay takes advantage of a molecules property to emit light of one specific wavelength while absorbing light of a different wavelength. This feature is given by a various amount of proteins, like GFP, RFP, etc. so that these peptides can be used as report proteins to detect other proteins by a fluorescence assay.  
+
The fluorescence assay takes advantage of the property of certain molecules to emit light of one specific wavelength while absorbing light of a different wavelength. This feature is also found in several proteins, like GFP or RFP, so these molecules can be used as reporter proteins to detect other proteins with a fluorescence assay by crating fusion proteins.  
-
For the fluorescence assay we had the [http://www.tecan.com/platform/apps/product/index.asp?MenuID=1812&ID=1916&Menu=1&Item=21.2.10.1 Infinite<html>&reg;</html> M200 platereader] by Tecan and the [http://www.gelifesciences.com/aptrix/upp01077.nsf/Content/2d_electrophoresis~scanners~typhoon_9400?OpenDocument&parentid=286927&moduleid=166668 Typhoon<html>&#153;</html> 9400] by GE Healthcare available.
+
For the fluorescence assay, we had the [http://www.tecan.com/platform/apps/product/index.asp?MenuID=1812&ID=1916&Menu=1&Item=21.2.10.1 Infinite<html>&reg;</html> M200 platereader] by Tecan and the [http://www.gelifesciences.com/aptrix/upp01077.nsf/Content/2d_electrophoresis~scanners~typhoon_9400?OpenDocument&parentid=286927&moduleid=166668 Typhoon<html>&#153;</html> 9400] by GE Healthcare available.
-
We used the fluorescence assay tho characterize the following BioBricks:
+
We used the fluorescence assay to characterize the following BioBricks:
<partinfo>K525121</partinfo>;
<partinfo>K525121</partinfo>;
<partinfo>K525123</partinfo>;
<partinfo>K525123</partinfo>;
Line 162: Line 174:
[[File:Bielefeld-Germany2011-FACS.png|200px|thumb|right|Our FACS device]]
[[File:Bielefeld-Germany2011-FACS.png|200px|thumb|right|Our FACS device]]
-
Flow cytometry describes a measurement method, which allows the analysis of cells that past an electronic detection apparatus or a light beam at high speed. Depending on the shape, structure or coloration of the cells, different effects are generated, from which the properties of the cell can be derived.
+
Flow cytometry describes a measurement method, that allows the analysis of cells which pass an electronic detection apparatus or a light beam at high speed. Depending on the shape, structure or coloration of the cells, different effects are generated, from which the properties of the cell can be derived.
-
In our case, we used the [http://www.bdbiosciences.com/instruments/facscalibur/index.jsp FACSCalibur flow cytometer] by BD Biosciences to analyze the formation of our S-Layers on the surface of the silica beads.
+
In our case, we used the [http://www.bdbiosciences.com/instruments/facscalibur/index.jsp FACSCalibur flow cytometer] by BD Biosciences to analyze the formation of our S-layers on the surface of the silica beads.
Line 177: Line 189:
===AFM===
===AFM===
-
Atomic force microscopy (AFM) is a special type of scanning probe microscopy, with a gained resolution below a nanometer, a thousand times higher than the optical diffraction limit. During the measurement, a nanosized needle, fixed on a leaf spring, is performed across the surface of a probe. The leaf spring is bent in different amplitudes, depending on the surface structure of the sample. This bending or deflection of the spring can be measured with optical sensors and is a result of the atomic forces, occurring between the needle and the surface. By recording the deflections respective forces point by point, an image of the sample surface is generated like a digital photo while each pixel stands for a specific physical or chemical parameter. The possible resolution is determined by the radius of curvature of the spring leaf and ranges from 0.1 to 10 nm. Thus, the atomic force microscope reaches the highest resolution of any microscopic technique.
+
Atomic force microscopy (AFM) is a special type of scanning probe microscopy, with a gained resolution below a nanometer, a thousand times higher than the optical diffraction limit. During the measurement, a nanosized needle, fixed on a leaf spring, is directed across the surface of a probe. The leaf spring is bent in different amplitudes, depending on the surface structure of the sample. This bending or deflection of the spring can be measured with optical sensors and is a result of the atomic forces, occurring between the needle and the surface. By recording the deflections respective forces point by point, an image of the sample surface is generated like a digital photo with each pixel being an illustration of a specific physical or chemical parameter. The possible resolution is determined by the radius of curvature of the spring leaf and ranges from 0.1 to 10 nm. Thus, the atomic force microscope reaches the highest resolution of any microscopic technique.

Latest revision as of 21:48, 28 October 2011

Contents

PCR

One of our PCR devices
Our real-time PCR device

The polymerase chain reaction (PCR) is a method to reproduce DNA in vitro. An enzyme, the polymerase, is used for this purpose. The term "chain reaction" in this context means, that the products of previous cycles are used as template for the next cycle and thus exponential amplification of specific DNA fragments is achieved. The formed DNA product results from defined primers, which are the start point for the polymerase.

The PCR is used in biological and medical laboratories for a variety of different tasks. In our case we used the PCR for two different applications. It is possible to check successful cloning when using primers that bind at the prefix and suffix regions of the cloning plasmid and separate/analyze the PCR product by agarose gel electrophoresis (Colony PCR). The other application is the amplification and cloning of genomic DNA. We further used our thermocyclers for the qualification of our molecular beacons. A thermal profile was taken by measuring the fluorescence of the molecular beacons as a function of temperature by a real-time PCR device.

For the colony PCR we used the [http://www.biometra.com/thermocycler-silver.0.html TProfessional Thermocycler] by Biometra and the [http://www.analytik-jena.com/en/LifeScience-AnalytikJenaAG/Products-/Instruments/Thermal-cycler__2266/ FlexCycler] by Analytik Jena. The thermal profile assay was performed with the [http://www.roche-applied-science.com/sis/rtpcr/htc/index.jsp LightCycler® 480 System] by Roche.


We used the PCR to characterize the following BioBricks: <partinfo>K525001</partinfo>; <partinfo>K525002</partinfo>; <partinfo>K525005</partinfo>; <partinfo>K525006</partinfo>; <partinfo>K525007</partinfo>; <partinfo>K525008</partinfo>; <partinfo>K525009</partinfo>; <partinfo>K525010</partinfo>; <partinfo>K525121</partinfo>; <partinfo>K525123</partinfo>; <partinfo>K525221</partinfo>; <partinfo>K525222</partinfo>; <partinfo>K525223</partinfo>; <partinfo>K525224</partinfo>; <partinfo>K525234</partinfo>; <partinfo>K525301</partinfo>; <partinfo>K525303</partinfo>; <partinfo>K525304</partinfo>; <partinfo>K525305</partinfo>; <partinfo>K525306</partinfo>; <partinfo>K525311</partinfo>; <partinfo>K525312</partinfo>; <partinfo>K525401</partinfo>; <partinfo>K525403</partinfo>; <partinfo>K525404</partinfo>; <partinfo>K525405</partinfo>; <partinfo>K525406</partinfo>; <partinfo>K525411</partinfo>; <partinfo>K525412</partinfo>; <partinfo>K525499</partinfo>; <partinfo>K525512</partinfo>; <partinfo>K525515</partinfo>; <partinfo>K525517</partinfo>; <partinfo>K525551</partinfo>; <partinfo>K525560</partinfo>; <partinfo>K525562</partinfo>; <partinfo>K525582</partinfo>; <partinfo>K525710</partinfo>; <partinfo>K525720</partinfo>; <partinfo>K525730</partinfo>; <partinfo>K525740</partinfo>; <partinfo>K525998</partinfo>; <partinfo>K525999</partinfo>


HPLC

High performance liquid chromatography (HPLC), a sort of liquid chromatography, is an analytical method in chemistry, not only to separate substances, but also to identify and quantify these substances using internal standards.

Our HPLC device

The examined substance, together with a mobile phase, is pumped through a separation column, the stationary phase. You can classify an HPLC according to the principle of separation in normal phase (NP), reverse phase (RP), ion exchange (IEC), size exclusion (SEC) and chiral chromatography. The substance to be tested is injected into the stream of the mobile phase in small amounts. The movement of the sample through the column depends on the nature of the sample on the one hand and the stationary phase on the other hand. If one component of the tested substance interacts strongly with the stationary phase, it remains on the column relatively long. If the interaction of a substance is weak, its velocity to leave the column is higher. The time at which a specific substance elutes is called retention time and is suitable for identification under particular conditions.

You can find the specifications of our HPLC device here.


We used the HPLC to characterize the following BioBricks: <partinfo>K525311</partinfo>; <partinfo>K525512</partinfo>; <partinfo>K525515</partinfo>; <partinfo>K525517</partinfo>; <partinfo>K525551</partinfo>; <partinfo>K525560</partinfo>; <partinfo>K525562</partinfo>; <partinfo>K525582</partinfo>


MS/MS

Tandem mass spectrometry (MS/MS) is an analytical physics technique with multiple mass spectrometry sections combined. Between two analyzers, a collision cell is mounted to apply energy to the ions by colliding them with an inert gas (usually nitrogen or argon). Thereafter the ions disintegrate very specific to other, lighter ions.


LC-MS

Our LC-ESI-qTOF-MS device

Liquid chromatography–mass spectrometry (LC-MS), a sort of tandem mass spectrometry, is an analytical chemistry technique which combines the physical separation of liquid chromatography (LC or HPLC) with the analysis of the substances by mass spectrometry (MS).

For the LC-ESI-qTOF-MS we had the [http://www.bdal.com/products/lc-ms/o-tof/microtof-q-ii/overview.html micrOTOF-Q II™] by Bruker Daltonics available.


We used an LC-ESI-qTOF-MS to characterize the following BioBricks: <partinfo>K525512</partinfo>; <partinfo>K525515</partinfo>; <partinfo>K525517</partinfo>


MALDI-TOF

Matrix-assisted Laser Desorption/Ionization – Time of flight (MALDI-TOF) is a procedure to analyze large biomolecules by their mass.

Our MALDI-TOF device

Before measurement, the analyte is co-crystallized on a metal plate within a solid matrix. 3,5-dimethoxy-4-hydroxycinnamic acid (sinapinic acid) and 2,5-dihydroxybenzoic acid (DHB) are most commonly used. Desorption of the analyte is taken by a laser beam, commonly with a wavelength of 337 nm. The matrix absorbs the laser light and the upper layer explosively vaporizes, ejecting both, matrix and analyte molecules. In addition to this vaporization, the laser beam also leads to an ionization of the analytes. The mass analysis is performed by the TOF (time of flight)-analysator. The evaporated ions are accelerated in an electric field. Typical acceleration voltages for this are 10-30 kV. The velocity of an ion depends on its mass and the charge. An ion detector converts the incoming ions into an electrical signal. The advantage of this method is the rapid analysis of a relatively large mass range.

The MALDI-TOF analysis was performed with the [http://www.bdal.com/products/maldi/ultraflextreme-series/overview.html ultrafleXtreme™] by Bruker Daltonics.


We used the MALDI-TOF Analysis to characterize the following BioBricks: <partinfo>K525121</partinfo>; <partinfo>K525123</partinfo>; <partinfo>K525221</partinfo>; <partinfo>K525222</partinfo>; <partinfo>K525223</partinfo>; <partinfo>K525224</partinfo>; <partinfo>K525710</partinfo>



Fluorescence Assay

One of our fluorescence assay devices

The fluorescence assay takes advantage of the property of certain molecules to emit light of one specific wavelength while absorbing light of a different wavelength. This feature is also found in several proteins, like GFP or RFP, so these molecules can be used as reporter proteins to detect other proteins with a fluorescence assay by crating fusion proteins.

For the fluorescence assay, we had the [http://www.tecan.com/platform/apps/product/index.asp?MenuID=1812&ID=1916&Menu=1&Item=21.2.10.1 Infinite® M200 platereader] by Tecan and the [http://www.gelifesciences.com/aptrix/upp01077.nsf/Content/2d_electrophoresis~scanners~typhoon_9400?OpenDocument&parentid=286927&moduleid=166668 Typhoon™ 9400] by GE Healthcare available.


We used the fluorescence assay to characterize the following BioBricks: <partinfo>K525121</partinfo>; <partinfo>K525123</partinfo>; <partinfo>K525221</partinfo>; <partinfo>K525222</partinfo>; <partinfo>K525223</partinfo>; <partinfo>K525224</partinfo>; <partinfo>K525304</partinfo>; <partinfo>K525305</partinfo>; <partinfo>K525306</partinfo>; <partinfo>K525404</partinfo>; <partinfo>K525405</partinfo>; <partinfo>K525406</partinfo>; <partinfo>K525710</partinfo>; <partinfo>K525740</partinfo>;



Luminescence Assay

Our luminescence assay device

The luminescence assay uses the ability of specific enzyme reactions to produce light for the measuring of product formation. On the other hand, this assay can also be used to detect enzymes or substrates which are required for these reactions.

For the luminescence assay we had the [http://www.promega.com/b/de/Glomax/glomax_multi.aspx GloMax®-Multi Detection System] by Promega available.


We used the Luminescence assay tho characterize the following BioBricks: <partinfo>K525311</partinfo>; <partinfo>K525411</partinfo>; <partinfo>K525710</partinfo>; <partinfo>K525740</partinfo>; <partinfo>K525999</partinfo>


FACS

Our FACS device

Flow cytometry describes a measurement method, that allows the analysis of cells which pass an electronic detection apparatus or a light beam at high speed. Depending on the shape, structure or coloration of the cells, different effects are generated, from which the properties of the cell can be derived.

In our case, we used the [http://www.bdbiosciences.com/instruments/facscalibur/index.jsp FACSCalibur flow cytometer] by BD Biosciences to analyze the formation of our S-layers on the surface of the silica beads.


We used the flow cytometry analysis to characterize the following BioBricks: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525305 BBa_K525305];



Microscopy

AFM

Atomic force microscopy (AFM) is a special type of scanning probe microscopy, with a gained resolution below a nanometer, a thousand times higher than the optical diffraction limit. During the measurement, a nanosized needle, fixed on a leaf spring, is directed across the surface of a probe. The leaf spring is bent in different amplitudes, depending on the surface structure of the sample. This bending or deflection of the spring can be measured with optical sensors and is a result of the atomic forces, occurring between the needle and the surface. By recording the deflections respective forces point by point, an image of the sample surface is generated like a digital photo with each pixel being an illustration of a specific physical or chemical parameter. The possible resolution is determined by the radius of curvature of the spring leaf and ranges from 0.1 to 10 nm. Thus, the atomic force microscope reaches the highest resolution of any microscopic technique.


We used the AFM to characterize the following BioBricks: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525301 BBa_K525301]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525303 BBa_K525303]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525304 BBa_K525304]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525305 BBa_K525305]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525306 BBa_K525306]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525311 BBa_K525311]

CLSM

Confocal laser scanning microscopy (CLSM) is a type of confocal microscopy, whereas, in contrast to the normal conventional light microscopy, not the entire sample is illuminated, but only a fraction, in most cases only a limited spot. The intensities of light reflected or emitted are measured consecutively at all locations of the sample, so that a subsequent construction of the image is possible.

The CLSM was performed with the [http://www.zeiss.de/c12567be00459794/Contents-Frame/377f01c62dc109cec12574e10035d20a LSM 700] by Zeiss.


We used the CLSM to characterize the following BioBricks: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525301 BBa_K525301]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525303 Baa_K525303]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525304 BBa_K525304]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525305 BBa_K525305]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525306 BBa_K525306]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525311 BBa_K525311]

SEM

Scanning electron microscopy (SEM) is a type of electron microscopy, where a beam of high-energy electrons is directed across the surface of a sample to be imaged in a raster scan pattern. The interactions between the electrons and the surface of the object can be measured and are used to generate an image of the sample. The maximum theoretical magnification factor is approximately about 1,000,000:1.

The SEM was performed with the [http://www.zeiss.de/c1256e4600305472/Contents-Frame/84e6e310b4773cb3c1256e54003a31fe EVO® MA] by Zeiss.


We used the SEM to characterize the following BioBricks: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525301 BBa_K525301]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525303 Baa_K525303]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525304 BBa_K525304]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525305 BBa_K525305]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525306 BBa_K525306]; [http://partsregistry.org/wiki/index.php?title=Part:BBa_K525311 BBa_K525311]

References

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M. H. Gey: Instrumentelle Analytik und Bioanalytik, 2. Aufl., Springer Verlag, Berlin 2008.

C. Hamann, M. Hietschold: Raster-Tunnel-Mikroskopie. Akademie Verlag, Berlin 1991, ISBN 3-05-501272-0.

Handbook of biological Confocal Microscopy, 3rd ed., Springer-Verlag, New York 2006, ISBN 978-0-387-25921-5

J. R. Lakowicz: Principles of fluorescence spectroscopy. Springer 2006, ISBN 9780387312781.

C. Mülhardt: Der Experimentator: Molekularbiologie / Genomics. 6. Aufl., Spektrum Akademischer Verlag, 2008, ISBN 978-3-8274-2036-7.

M. G. Ormerod (ed.): Flow Cytometry — A practical approach. 3rd edition, Oxford University Press, Oxford (UK.) 2000, ISBN 0199638241

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