User:Irina Petrova

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[[image: Ira2.jpg|left|thumb|200px| Irina Petrova]]
[[image: Ira2.jpg|left|thumb|200px| Irina Petrova]]
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email: irina.petrova(at)biologie.uni-freiburg.de
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<br><br>
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I am a PhD student of the GRK 1305/1 “Plant Signal Systems” program in Freiburg University[http://www.plant-signals.uni-freiburg.de/]. I am working on the detection and visualization of Arabidopsis thaliana root mRNA in Prof. Palme’s research group[http://www.biologie.uni-freiburg.de/forschung/botanik.php]. I am interested in bringing science and design together. I like DNA and the iGEM Competition.
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email: <font color='green'>irina.petrova(at)biologie.uni-freiburg.de</font color>
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==== Individual project: <font color='blue'>Nike nano collection (Blouse and Skirt)</font color> ====
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==== Individual project: <font color='blue'>Nike Blouse</font color> ====
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The dress design is more interesting than a chip design (in my opinion ;). It is very individual and very fashionable. We want to follow fashion, don’t we?
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The dress design is more interesting than a chip design (to my opinion ;). It is very individual and very fashionable. We want to follow the fashion, don’t we?
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On the other hand, a broad range of variable forms can be important for an artificial life. I play with DNA like with my Barbie doll.
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On another hand, a broad range of variable forms can be important for an artificial life. I play with DNA like with my Barbie doll.
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The idea was to knit a nice blouse for Barbie without any boundary conditions. I used two methods of knitting: <br>
The idea was to knit a nice blouse for Barbie without any boundary conditions. I used two methods of knitting: <br>
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1) rectangular merge pattern, and <br>
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1) a rectilinear merge pattern, and <br>
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2) staggered merge pattern <br>
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2) a staggered merge pattern <br>
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In the terms of Paul Rothemund. The first one is simpler for understanding; the second one is more practical for patterning. Only if you used the staggered merge pattern, you can put all hairpins onto one side of the knitted DNA sheet with a maximal density.
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following the terms of Paul Rothemund. The first one is simpler to understand; the second one is more practical for patterning. Only when you use a staggered merge pattern can you put all hairpins onto one side of the knitted DNA sheet with maximal density.
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Have a look on the pictures: <br>
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Have a look at the pictures: <br>
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(More details will be available soon)
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[[image:Blouse_rect.jpg|left|thumb|314px|Blouse with rectilinear merge pattern]]
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[[image:Bluse1.jpg|left|thumb|200px|Bluse on the wall]]  
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[[image:Blouse_stag.jpg|left|thumb|291px|Blouse with staggered merge pattern]]
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[[image:Bluse2.jpg|left|thumb|250px|Bluse on the table]]  
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[[image:skirt.jpg|left|thumb|640px|Skirt with staggered merge pattern]]
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<br style="clear:both;"/>
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I use the fork hairpin  
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This design is for [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/sequences/m13mp18.txt M13mp18] scaffold DNA. I use the fork hairpin  
[http://partsregistry.org/Part:BBa_J35001 BBa_J35001]   
[http://partsregistry.org/Part:BBa_J35001 BBa_J35001]   
to create the Nike-logo pattern. <br>
to create the Nike-logo pattern. <br>
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Other ones would be:  
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The other ones would be:  
[http://partsregistry.org/Part:BBa_J35003 BBa_J35003],  
[http://partsregistry.org/Part:BBa_J35003 BBa_J35003],  
[http://partsregistry.org/Part:BBa_J35004 BBa_J35004],
[http://partsregistry.org/Part:BBa_J35004 BBa_J35004],
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[http://partsregistry.org/Part:BBa_J35006 BBa_J35006],
[http://partsregistry.org/Part:BBa_J35006 BBa_J35006],
[http://partsregistry.org/Part:BBa_J35007 BBa_J35007]. <br>
[http://partsregistry.org/Part:BBa_J35007 BBa_J35007]. <br>
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Your choose!
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Your choice!  
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My photos will help you.
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<gallery>
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Image:picture01.jpg
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Image:picture02.jpg
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Image:picture03.jpg
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Image:picture04.jpg
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Image:4_fingers_arm.gif|[http://partsregistry.org/Part:BBa_J35004 BBa_J35004]
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Image:5_fingers_arm.gif|[http://partsregistry.org/Part:BBa_J35005 BBa_J35005]
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Image:6_fingers_arm.gif|[http://partsregistry.org/Part:BBa_J35006 BBa_J35006]
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Image:7_fingers_arm.gif|[http://partsregistry.org/Part:BBa_J35007 BBa_J35007]
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</gallery>
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Another pretty possibility is the hybrids (color)FP with DNA-binding proteins that bind to specific staples, e.g. [http://partsregistry.org/Part:BBa_J35030 BBa_J35030]
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[http://2006.igem.org/wiki/index.php/Freiburg_University_2006 Home]
[http://2006.igem.org/wiki/index.php/Freiburg_University_2006 Home]

Latest revision as of 15:35, 20 December 2006

Irina Petrova



I am a PhD student of the GRK 1305/1 “Plant Signal Systems” program in Freiburg University[http://www.plant-signals.uni-freiburg.de/]. I am working on the detection and visualization of Arabidopsis thaliana root mRNA in Prof. Palme’s research group[http://www.biologie.uni-freiburg.de/forschung/botanik.php]. I am interested in bringing science and design together. I like DNA and the iGEM Competition.


email: irina.petrova(at)biologie.uni-freiburg.de


Individual project: Nike nano collection (Blouse and Skirt)

The dress design is more interesting than a chip design (in my opinion ;). It is very individual and very fashionable. We want to follow fashion, don’t we?

On the other hand, a broad range of variable forms can be important for an artificial life. I play with DNA like with my Barbie doll.

The idea was to knit a nice blouse for Barbie without any boundary conditions. I used two methods of knitting:
1) a rectilinear merge pattern, and
2) a staggered merge pattern
following the terms of Paul Rothemund. The first one is simpler to understand; the second one is more practical for patterning. Only when you use a staggered merge pattern can you put all hairpins onto one side of the knitted DNA sheet with maximal density.

Have a look at the pictures:

Blouse with rectilinear merge pattern
Blouse with staggered merge pattern
Skirt with staggered merge pattern


This design is for [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/sequences/m13mp18.txt M13mp18] scaffold DNA. I use the fork hairpin [http://partsregistry.org/Part:BBa_J35001 BBa_J35001] to create the Nike-logo pattern.
The other ones would be: [http://partsregistry.org/Part:BBa_J35003 BBa_J35003], [http://partsregistry.org/Part:BBa_J35004 BBa_J35004], [http://partsregistry.org/Part:BBa_J35005 BBa_J35005], [http://partsregistry.org/Part:BBa_J35006 BBa_J35006], [http://partsregistry.org/Part:BBa_J35007 BBa_J35007].
Your choice!

My photos will help you.

Picture01.jpg
Picture02.jpg
Picture03.jpg
Picture04.jpg

[http://partsregistry.org/Part:BBa_J35004 BBa_J35004]

[http://partsregistry.org/Part:BBa_J35005 BBa_J35005]

[http://partsregistry.org/Part:BBa_J35006 BBa_J35006]

[http://partsregistry.org/Part:BBa_J35007 BBa_J35007]

Another pretty possibility is the hybrids (color)FP with DNA-binding proteins that bind to specific staples, e.g. [http://partsregistry.org/Part:BBa_J35030 BBa_J35030]

[http://2006.igem.org/wiki/index.php/Freiburg_University_2006 Home]

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