User:Irina Petrova
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email: <font color='green'>irina.petrova(at)biologie.uni-freiburg.de</font color> | 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> ==== | ==== Individual project: <font color='blue'>Nike nano collection (Blouse and Skirt)</font color> ==== | ||
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[[image:skirt.jpg|left|thumb|658px|Skirt with staggered merge pattern]] | [[image:skirt.jpg|left|thumb|658px|Skirt with staggered merge pattern]] | ||
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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 | This design is for [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/sequences/m13mp18.txt M13mp18] scaffold DNA. I use the fork hairpin | ||
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Image:7_fingers_arm.gif|BBa_J35007 | Image:7_fingers_arm.gif|BBa_J35007 | ||
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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] | ||
Revision as of 10:19, 30 October 2006
I am a PhD student of the GRK 1305/1 “Plant Signal Systems” program in Freiburg University[1]. I work on detection and visualization of Arabidopsis thaliana root mRNA in Prof. Palme’s research group[2]. I am interested in bringing science and design together. I like DNA and 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 (to my opinion ;). It is very individual and very fashionable. We want to follow the fashion, don’t we?
On the another 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) rectilinear merge pattern, and
2) staggered merge pattern
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.
Have a look on the pictures:
This design is for M13mp18 scaffold DNA. I use the fork hairpin
BBa_J35001
to create the Nike-logo pattern.
Other ones would be:
BBa_J35003,
BBa_J35004,
BBa_J35005,
BBa_J35006,
BBa_J35007.
Your choose!
My photos will help you.
 |
 |
 |
 |
 BBa_J35004 |
 BBa_J35005 |
 BBa_J35006 |
 BBa_J35007 |
Another pretty possibility is the hybrids (color)FP with DNA-binding proteins that bind to specific staples, e.g. BBa_J35030
