[DIYbio] Re: Power tool analogue in MolBio.

Like what Koeng said. Leucin zippers seem what you're looking for?

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[DIYbio] Re: Power tool analogue in MolBio.

Like what Koeng said. Leucin zippers seem what you're looking for?

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[DIYbio] Re: Power tool analogue in MolBio.

Like what Koeng said. Leucin zippers seem what you're looking for?

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[DIYbio] Re: Power tool analogue in MolBio.

What exactly do you want it to do? There are leucine zippers or TALENS or CRISPR, inteins and GS linkers, his tags or FLAG tags, biotin and streptavidin, introns or ribozymes... Each has a specific purpose. And for the termini, yes most likely, unless you want to go through some protein engineering and structure analysis to see if it would fold correctly.

Maybe this will be a lead for the inteins, if you just want a specific protein to fuse to something modularly - http://2014.igem.org/Team:Heidelberg/Parts .

-Koeng
On Saturday, October 31, 2015 at 12:13:18 PM UTC-7, Yuriy wrote:

Hello everyone.


I'll try to be as brief as possible, given the lack of knowledge on the subject. I don't know where to start. That's why I came here with the question.


I was looking at my drill and it dawned on me that there isn't anything like it, to my knowledge, in molecular biology. It is a tool that alone has no use but given the proper fittings and combination of tool:fittings (adapters), can get the job done. The drill bit end for example, has six sides that accommodate the adjustable chuck. That's what I was looking into for the last few days.


Is there a good, on both transcribed, antibody to antigen fitting to adapt fitting to a molecular tool?


If yes do they have to be on termini? Or can it jet out of aa design via linkers?


I essentially need the tool that will be stable in vivo, while the adapters can undergo a higher turnover under different environmental ques.


Just looking for a good non-bulky-lock and key to be encoded for the tool set.


-Yuriy

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Re: [DIYbio] Power tool analogue in MolBio.

No but biotinylation of a protein is easy peasy

Sent from my T-Mobile Android device

On Oct 31, 2015 3:57 PM, Yuriy <yuriyology@gmail.com> wrote:
Biotin is not transcribed, is it?

On Saturday, October 31, 2015 at 3:18:56 PM UTC-4, incisive systematics wrote:

Biotin / streptavidin come to mind .... Just at first pass. ....
>matt

Sent from my T-Mobile Android device

On Oct 31, 2015 3:15 PM, Yuriy <yuriy...@gmail.com> wrote:

Hello everyone.


I'll try to be as brief as possible, given the lack of knowledge on the subject. I don't know where to start. That's why I came here with the question.


I was looking at my drill and it dawned on me that there isn't anything like it, to my knowledge, in molecular biology. It is a tool that alone has no use but given the proper fittings and combination of tool:fittings (adapters), can get the job done. The drill bit end for example, has six sides that accommodate the adjustable chuck. That's what I was looking into for the last few days.


Is there a good, on both transcribed, antibody to antigen fitting to adapt fitting to a molecular tool?


If yes do they have to be on termini? Or can it jet out of aa design via linkers?


I essentially need the tool that will be stable in vivo, while the adapters can undergo a higher turnover under different environmental ques.


Just looking for a good non-bulky-lock and key to be encoded for the tool set.


-Yuriy

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Re: [DIYbio] Power tool analogue in MolBio.

Biotin is not transcribed, is it?

On Saturday, October 31, 2015 at 3:18:56 PM UTC-4, incisive systematics wrote:

Biotin / streptavidin come to mind .... Just at first pass. ....
>matt

Sent from my T-Mobile Android device

On Oct 31, 2015 3:15 PM, Yuriy <yuriy...@gmail.com> wrote:

Hello everyone.


I'll try to be as brief as possible, given the lack of knowledge on the subject. I don't know where to start. That's why I came here with the question.


I was looking at my drill and it dawned on me that there isn't anything like it, to my knowledge, in molecular biology. It is a tool that alone has no use but given the proper fittings and combination of tool:fittings (adapters), can get the job done. The drill bit end for example, has six sides that accommodate the adjustable chuck. That's what I was looking into for the last few days.


Is there a good, on both transcribed, antibody to antigen fitting to adapt fitting to a molecular tool?


If yes do they have to be on termini? Or can it jet out of aa design via linkers?


I essentially need the tool that will be stable in vivo, while the adapters can undergo a higher turnover under different environmental ques.


Just looking for a good non-bulky-lock and key to be encoded for the tool set.


-Yuriy

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Re: [DIYbio] Power tool analogue in MolBio.

Biotin / streptavidin come to mind .... Just at first pass. ....
>matt

Sent from my T-Mobile Android device

On Oct 31, 2015 3:15 PM, Yuriy <yuriyology@gmail.com> wrote:

Hello everyone.


I'll try to be as brief as possible, given the lack of knowledge on the subject. I don't know where to start. That's why I came here with the question.


I was looking at my drill and it dawned on me that there isn't anything like it, to my knowledge, in molecular biology. It is a tool that alone has no use but given the proper fittings and combination of tool:fittings (adapters), can get the job done. The drill bit end for example, has six sides that accommodate the adjustable chuck. That's what I was looking into for the last few days.


Is there a good, on both transcribed, antibody to antigen fitting to adapt fitting to a molecular tool?


If yes do they have to be on termini? Or can it jet out of aa design via linkers?


I essentially need the tool that will be stable in vivo, while the adapters can undergo a higher turnover under different environmental ques.


Just looking for a good non-bulky-lock and key to be encoded for the tool set.


-Yuriy

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[DIYbio] Power tool analogue in MolBio.

Hello everyone.


I'll try to be as brief as possible, given the lack of knowledge on the subject. I don't know where to start. That's why I came here with the question.


I was looking at my drill and it dawned on me that there isn't anything like it, to my knowledge, in molecular biology. It is a tool that alone has no use but given the proper fittings and combination of tool:fittings (adapters), can get the job done. The drill bit end for example, has six sides that accommodate the adjustable chuck. That's what I was looking into for the last few days.


Is there a good, on both transcribed, antibody to antigen fitting to adapt fitting to a molecular tool?


If yes do they have to be on termini? Or can it jet out of aa design via linkers?


I essentially need the tool that will be stable in vivo, while the adapters can undergo a higher turnover under different environmental ques.


Just looking for a good non-bulky-lock and key to be encoded for the tool set.


-Yuriy

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Re: [DIYbio] Re: The ODIN Needs Your Help - T4 DNA Ligase Testing - Free Ligase

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453199/ It makes a lot of sense that these people recommend 19 base pairs. 

It's also definitely not just blunt end ligation, you can check out the data just in that paper, where they did control for that. I agree that I would need more controls to get decent results, I simply didn't think that it'd work this well. I'll update once I get those results (in the next few weeks I am definitely going to do more controlled experiments).

-Koeng

On Friday, October 30, 2015 at 1:22:57 PM UTC-7, Bryan Jones wrote:
I'm not an expert on reading patents, but it looks like the patent covers the method of the cloning procedure, not the production of SLiCE extract, nor the composition matter of SLiCE extract. Selling the SLiCE mix might not actually violate the patent (that'd be up to the user to do or not do). It also looks like the the patent only covers assembly of fragments that have "20 bp to 52 bp that are homologous". So using 19bp or 53bp homologous regions might be a way around the patent. Maybe a bit less efficient, but it looks like that would still work.
On Fri, Oct 30, 2015 at 3:03 PM Koeng <koen...@gmail.com> wrote:
Yea, my apologies for the non-controlled experiment, I didn't set it up to be very controlled because I didn't think I'd get that good of efficiency. I will be running a few more in the next few weeks so I will post the results. 

Unfortunately enough, it appears that SLiCE is patented ( http://www.google.com/patents/US20130045508 ), and the company that owns the patent charges an arm and a leg ( http://slicecloning.com/SLiCE.html , more than HiFi mix per reaction). I guess the ODIN can't sell the mix, but possibly sell a kit to make it yourself.

-Koeng


On Thursday, October 29, 2015 at 3:12:01 PM UTC-7, Josiah Zayner wrote:
This is pretty cool. If people try and repeat these experiments can they post detailed details(heh) of what they did so others can follow suite.

Also, it doesn't seem anyone is running the control of everything but the SLiCE mixture. If you are running an experiment can you do that and let us know how that goes?

Thanks,
     Josiah

On Thu, Oct 29, 2015 at 2:44 PM, Koeng <koen...@gmail.com> wrote:
I tried out my homemade SLiCE mix. I put 100ng of both insert and vector in for a 2 piece assembly, for 30 minutes. I compared it to some homemade Gibson mix.

On my plates, I got 13 colonies on the SLiCE plate and 42 colonies on the Gibson. I am extremely impressed with 1/3 considering just the simple strain and simple lysis procedure.

-Koeng

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Re: [DIYbio] Re: The ODIN Needs Your Help - T4 DNA Ligase Testing - Free Ligase

Yeah, don't know if I am interested in selling a SLiCE mix because I still don't know how efficient it is in a DIY setting. That is why I am interested in the results you all are having. And what you all are using, i.e. homemade competent cells vs. high efficiency competent cells, &c. Is just some blunt end ligation occurring or is it an actually legit Gibson like assembly? I will test it out in a few weeks.

Patents don't really hold me back from biology stuff, maybe they should? They say the patent applies to every RecA- bacterial strain but have only tested 5-10? The patent seems flimsy with so many ways around it. Just don't list the bacteria I use? or Use a bacterial strain isolated from my skin that 16s is not an identical match for any known bacteria. They seem like a small company that probably doesn't have enough money to sue and would probably gain very little in damages. But who knows.



On Fri, Oct 30, 2015 at 1:22 PM, Bryan Jones <bryanjjones@gmail.com> wrote:
I'm not an expert on reading patents, but it looks like the patent covers the method of the cloning procedure, not the production of SLiCE extract, nor the composition matter of SLiCE extract. Selling the SLiCE mix might not actually violate the patent (that'd be up to the user to do or not do). It also looks like the the patent only covers assembly of fragments that have "20 bp to 52 bp that are homologous". So using 19bp or 53bp homologous regions might be a way around the patent. Maybe a bit less efficient, but it looks like that would still work.
On Fri, Oct 30, 2015 at 3:03 PM Koeng <koeng101@gmail.com> wrote:
Yea, my apologies for the non-controlled experiment, I didn't set it up to be very controlled because I didn't think I'd get that good of efficiency. I will be running a few more in the next few weeks so I will post the results. 

Unfortunately enough, it appears that SLiCE is patented ( http://www.google.com/patents/US20130045508 ), and the company that owns the patent charges an arm and a leg ( http://slicecloning.com/SLiCE.html , more than HiFi mix per reaction). I guess the ODIN can't sell the mix, but possibly sell a kit to make it yourself.

-Koeng


On Thursday, October 29, 2015 at 3:12:01 PM UTC-7, Josiah Zayner wrote:
This is pretty cool. If people try and repeat these experiments can they post detailed details(heh) of what they did so others can follow suite.

Also, it doesn't seem anyone is running the control of everything but the SLiCE mixture. If you are running an experiment can you do that and let us know how that goes?

Thanks,
     Josiah

On Thu, Oct 29, 2015 at 2:44 PM, Koeng <koen...@gmail.com> wrote:
I tried out my homemade SLiCE mix. I put 100ng of both insert and vector in for a 2 piece assembly, for 30 minutes. I compared it to some homemade Gibson mix.

On my plates, I got 13 colonies on the SLiCE plate and 42 colonies on the Gibson. I am extremely impressed with 1/3 considering just the simple strain and simple lysis procedure.

-Koeng

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Test Engineer.............Northridge, CA.............12+months

Urgent requirement

Please send resume @ bipin@tresourceinc.com 

Hi,

I have an urgent requirement with one of my clients, details given below. If you find yourself suitable for the position, please send me your latest updated resume along with contact details. Please include your employer details as well.

Job Title

Test Engineer

Project Location

Northridge, CA

Duration

12+months

 

Position Responsibilities:

  • Ability to visualize mechanical design solutions and translate them into manufacturable Designs.
  • Basic knowledge of material properties so data sheets can be interpreted and application specific materials are selected.
  • Knowledge of manufacturing processes such as milling, turning, broaching, wire EDM, injection molding, etc.
  • Design components, assemblies and fixtures using a 3D CAD package (e.g. SolidWorks)
  • Create and interpret 2-D drawings.
  • Set up test equipment for electromechanical tests, designing test plans, and executing tests.
  • Knowledge of Tolerance Analysis techniques to ensure multi-component designs function across tolerance spreads.
  • Perform basic Mechanical Engineering hand calculations, conduct FEA and use empirical data to justify own design solutions
  • Generate design review content to effectively communicate results, hurdles, and design solutions to senior staff in peer design reviews.
  • Generate Engineering Reports, Memo's, and Presentations.
  • Generate and execute test plans to demonstrate designs meet requirements

Basic Qualifications:

  • Bachelor's degree
  • Fundamental knowledge of Engineering Statistics.
  • Ability to communicate and work with internal and external staff to facilitate the procurement of physical parts from specifications and drawings.
  • Manage own time with the use of project management tools to accomplish departmental goes on schedule.
  • Ability to communicate, track, and report project progress.
  • Ability to interpret engineering standards and regulations (ASME, ASTM, IPC, IEC, etc.)
  • Basic understanding of electromechanical systems.

 

 

Thanks & Regards

 

BIPIN RAJ

Sr. US IT Recruiter (Talent Acquisition)

Technology Resource Group Inc

3736 Hills-Dale Court,
Santa Clara, CA 95051

Direct: 408-709-1760 Ext : 818,

 

G talk: bipin.rgtalent@gmail.com

bipin@tresourceinc.com

 

                                              www.tech-resource.com

 

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Re: [DIYbio] Re: The ODIN Needs Your Help - T4 DNA Ligase Testing - Free Ligase

I'm not an expert on reading patents, but it looks like the patent covers the method of the cloning procedure, not the production of SLiCE extract, nor the composition matter of SLiCE extract. Selling the SLiCE mix might not actually violate the patent (that'd be up to the user to do or not do). It also looks like the the patent only covers assembly of fragments that have "20 bp to 52 bp that are homologous". So using 19bp or 53bp homologous regions might be a way around the patent. Maybe a bit less efficient, but it looks like that would still work.
On Fri, Oct 30, 2015 at 3:03 PM Koeng <koeng101@gmail.com> wrote:
Yea, my apologies for the non-controlled experiment, I didn't set it up to be very controlled because I didn't think I'd get that good of efficiency. I will be running a few more in the next few weeks so I will post the results. 

Unfortunately enough, it appears that SLiCE is patented ( http://www.google.com/patents/US20130045508 ), and the company that owns the patent charges an arm and a leg ( http://slicecloning.com/SLiCE.html , more than HiFi mix per reaction). I guess the ODIN can't sell the mix, but possibly sell a kit to make it yourself.

-Koeng


On Thursday, October 29, 2015 at 3:12:01 PM UTC-7, Josiah Zayner wrote:
This is pretty cool. If people try and repeat these experiments can they post detailed details(heh) of what they did so others can follow suite.

Also, it doesn't seem anyone is running the control of everything but the SLiCE mixture. If you are running an experiment can you do that and let us know how that goes?

Thanks,
     Josiah

On Thu, Oct 29, 2015 at 2:44 PM, Koeng <koen...@gmail.com> wrote:
I tried out my homemade SLiCE mix. I put 100ng of both insert and vector in for a 2 piece assembly, for 30 minutes. I compared it to some homemade Gibson mix.

On my plates, I got 13 colonies on the SLiCE plate and 42 colonies on the Gibson. I am extremely impressed with 1/3 considering just the simple strain and simple lysis procedure.

-Koeng

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[DIYbio] Fwd: US Biotech Regulations -- your support is still needed!




From: Cornell Alliance for Science <allianceforsci@cornell.edu>
Sent: 30 October 2015 17:01:37 GMT+00:00
To: =?utf-8?Q??= <cathalgarvey@cathalgarvey.me>
Subject: US Biotech Regulations -- your support is still needed!

View this email in your browser

Dear Allies of Science,
 
Today, federal agencies in the United States will hear public comments regarding the review of the Coordinated Framework for the Regulation of Biotechnology. 

We need your input, comments and case studies as OSTP reviews the existing U.S. Coordinated Framework for the Regulation of BiotechnologyThe call for comments will end on November 13, so we still have a chance to ensure that scientists both working in the public sector and for small businesses have greater access to innovate using the tools of biotechnology.  

We plan to submit all of the comments that we receive as one package in order to amplify the support for public sector science. 

If you haven't done so already make your case study known using our petition:
http://cas.nonprofitsoapbox.com/usbiotechregulations
 
Now is the time for scientists to speak up and share their accounts of how the playing field could be leveled so that public sector scientists can innovate using all the tools available to deploy solutions much-needed in agricultural solutions. 
 
Make your voice heard to OSTP!
 
Yours,
Sarah Evanega and the Alliance for Science Team
 

 

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@ScienceAlly
Alliance Website






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