[DIYbio] Re: Biological Parts Registry Current State of Affairs

The Free Genes Project is just the kind of DNA distribution model I think biohackers should be pursuing. I sent a private email to discuss possible collaborations. Let me know about your priorities for types of genes and I can help do some R&D based on that.

On Thursday, April 11, 2019 at 1:18:52 PM UTC-4, Koeng wrote:

Eh basically given up. They have no plans on lowering their fees to entry, so it's not like many labs can afford to go, when they could be spending resources on actual projects. There isn't really the goal of innovating in bioengineering anymore on the institutional level: that stopped years ago when the original MIT folks went to do their own things (like Ginkgo). It's now much more about putting on a very nice show, which gets funders, so they can do a better show. 

I'm working on the FreeGenes project (have for a while) on building another parts repository that is actually open source (iGEM simply doesn't use terms or conditions with their plasmid stocks, we're using the OpenMTA). It turns out it's actually really hard to build large quantities of parts: for about a year we messed around with in house cloning, and got pretty far, but now we're just ordering clonal DNA directly from Twist. I'm beginning to hit on toolkits that are generally useful by spreading out the number of suppliers we have rather than cleverness to clone hard things in house, so it's just taking a while. It's also just hard to scale the DNA design process.

The FreeGenes parts collections aren't out yet, but will be sooner or later. For now, if you want parts and are unaffiliated with an institution, you either know people, get them from the odin, or get affiliated. 

koeng
On Wednesday, April 10, 2019 at 8:08:00 AM UTC-7, Christopher Monaco wrote:
Hi all,

I'm getting ready to gear up our synbio efforts at my DIYbio space and was looking iGEM and their biological parts registry as routes to go. It seems really difficult to have acess to the tools they offer and I'm honestly not sure if there's even a community iGEM track anymore. Based on posts on this mailing list (the most recent of which are several years old), it looks like the DIYbio community has more or less given up hope of having a working relationship with these folks. Which is a real shame because closing off access to parts from the public does not seem like any way to further the mission of innovating bioengineering.

Anyway, that long intro is to ask what are people in this community doing when wanting to perform synthetic biology? Is there another parts respository out there other than the one controlled by iGEM? Do you just have the requisite parts synthesized? I guess the big question is how can someone unaffiliated with an institution do work in this field?

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Re: [DIYbio] ReSeq crowd funder to write new software for HiSeq DNA sequencers

Thanks for the tips folks. I reached out to your suggestions. We are not tantalizingly close to making it!

On Saturday, April 27, 2019 at 4:33:57 PM UTC, Abizar Lakdawalla wrote:
Will Greenleaf at Stanford had hacked Illumina sequencers as imaging platforms. Might be worth contacting him.

On Sat, Apr 27, 2019 at 9:07 AM Dakota Hamill <dko...@gmail.com> wrote:
This guy is cool.  A lot of people I know in sequencing mention his blog.  (I know next to nothing about NGS).  Maybe he'd give you a shoutout, maybe not. 




On Sat, Apr 27, 2019 at 11:57 AM Kaspar Emanuel <kaspar...@gmail.com> wrote:
Hi folks,

John is right, the campaign is only for writing software to allow people to drive the machines. You will be able to use the Micromanager interface and scripting capabilities to do whatever you want, including patented procedures, if you can get your hands on the consumables and if you aren't exploiting them commercially, but IANAL, just a software developer.

Looks like this will be a close call as to whether we will reach our funding goal, any suggestions on where else to post are very much appreciated.

Cheers,

Kaspar

On Thursday, April 25, 2019 at 3:05:18 PM UTC, John Griessen wrote:
On 4/24/19 10:23 PM, Abizar Lakdawalla wrote:
> any plan on getting the consumables for the HiSeq? They cost US$10ks per run if they are bought from Illumina.

My take on reading the https://wemakeit.com/projects/reseq-reuse-dna-sequencers pages is that
components will be developed for uses first and maybe some day allow open uses, but not really in conflict with Illumina's
patents, and so not using their consumables.  They did not say they were going to make the machines run as they did
when new.

Driving them as an automated microscope was first on the to do list.

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[DIYbio] Re: in vitro CRISPR

google DNA guide CRISPR + add cas9, if you want. 

I must admit I thought you meant NgAgo (Argonaute) based CRISPR system but it looks like there really is a partial DNA based Cas9 guide system, with less off target activity than a simple CRISPR-Cas9. 

thanks for luring people to a new study on the subject. 

On Sunday, April 28, 2019 at 6:15:16 PM UTC-4, Andreas "Mega" Stuermer wrote:
Hi!

I remember a friend saying that the CRISPR-Cas9 protein can actually use ssDNA guides as opposed to RNA guides. Citation needed. 

Does anyone have experience with this? 

Considering this for science workshop, because if you are doing it in vitro, you don't get genetically modified organisms, and you can do it at any high school without a governmentally certified lab in Europe. 

Thanks! 

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Re: [DIYbio] 3D printer capable of printing autoclavable resin

Polycarbonate can work, but all polycarbonate filaments are not created equal. Some are will survive the autoclave well, while others will warp and distort. 
--Bryan Jones


On Mon, Apr 29, 2019 at 2:41 AM Jenny Molloy <jcmcoppice12@gmail.com> wrote:
Biomakespace have been testing some PP 3D prints in our autoclave with some success, there was no difference in integrity up to about 8 cycles (before someone emptied the autoclave without realising the test piece was in there and threw it away!)
There was an increase in what I can only describe as "tackiness" of the material though so you'd want to test that there isn't leaching from the outer layers that could mess with your assay.

We didn't have too much trouble printing with it using our Prusa i3 MK3 and we're planning a more thorough experiment with some tests for strength and deformity. I can find out the filament brand and printer settings from the member who was using it if that helps!

Jenny


On Saturday, 27 April 2019 15:18:06 UTC+1, Dakota Hamill wrote:
Making custom modification pieces to standard lab-ware to make certain assays easier to run.  Basically devices that come into contact with molten agar.  PP looks pretty finicky to print with. Polycarbonate looks easier to work with but will breakdown over repeated cycles and looks sensitive to pH swings?  We had someone print a mold and try to cast resin in it but the resin wasn't getting into all the nooks and crannies of the mold even with degassing it under vacuum.    Thank you for the suggestions will read more into PP as I trust the material, just finding the best printer for it I suppose. Or sucking it up and looking at a Formlabs



On Fri, Apr 26, 2019 at 10:29 PM Abizar Lakdawalla <abi...@gmail.com> wrote:
what are you trying to make? It may be easier to mill or machine polypropylene and polycarbonate. Polypropylene can withstand autoclaving but are difficult to 3D print. Polycarbonate can also withstand autoclaving and is easier to 3D print.

On Fri, Apr 26, 2019 at 6:29 PM Dakota Hamill <dko...@gmail.com> wrote:
Has anyone had any success with either heated extrusion or resin printers to create prints with resins capable of standing repeated autoclave cycles? 







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[DIYbio] Re: The possibility of DiY cannabinoid yeast

Definitely possible, but it takes a lot of work. A friend has been working on this and said that the difficulty is to get the yeast to produce enough to be commercially viable. Getting it to produce tiny ammounts shouldn't be too difficult. Also note, that these compunds are secreted from the plant cells because they are toxic to the cells in high concentrations, and act anti-microbial IIRC. Hence they won't be healthy for yeast. 

In any way, make sure to check your local regulation. I guess, as long as you produce CBD (the non-hallucinogenic medical compound) and no THC, it may be fine in many places. 





On Saturday, April 20, 2019 at 3:02:43 AM UTC+2, DiyBioMI wrote:
Hey, sorry for the delayed response.  It will be in Southeast MI. Starting small because I don't have funding to rent or buy a lab space yet.  I would like it to be a community lab once I get a space. I have a bunch of equipment already so I won't have to spend money on that.  For now I am set up at home and will be working on projects myself until friends or others that are interested come along.  

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[DIYbio] in vitro CRISPR

Hi!

I remember a friend saying that the CRISPR-Cas9 protein can actually use ssDNA guides as opposed to RNA guides. Citation needed. 

Does anyone have experience with this? 

Considering this for science workshop, because if you are doing it in vitro, you don't get genetically modified organisms, and you can do it at any high school without a governmentally certified lab in Europe. 

Thanks! 

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Re: [DIYbio] ReSeq crowd funder to write new software for HiSeq DNA sequencers

Will Greenleaf at Stanford had hacked Illumina sequencers as imaging platforms. Might be worth contacting him.

On Sat, Apr 27, 2019 at 9:07 AM Dakota Hamill <dkotes@gmail.com> wrote:
This guy is cool.  A lot of people I know in sequencing mention his blog.  (I know next to nothing about NGS).  Maybe he'd give you a shoutout, maybe not. 




On Sat, Apr 27, 2019 at 11:57 AM Kaspar Emanuel <kaspar.emanuel@gmail.com> wrote:
Hi folks,

John is right, the campaign is only for writing software to allow people to drive the machines. You will be able to use the Micromanager interface and scripting capabilities to do whatever you want, including patented procedures, if you can get your hands on the consumables and if you aren't exploiting them commercially, but IANAL, just a software developer.

Looks like this will be a close call as to whether we will reach our funding goal, any suggestions on where else to post are very much appreciated.

Cheers,

Kaspar

On Thursday, April 25, 2019 at 3:05:18 PM UTC, John Griessen wrote:
On 4/24/19 10:23 PM, Abizar Lakdawalla wrote:
> any plan on getting the consumables for the HiSeq? They cost US$10ks per run if they are bought from Illumina.

My take on reading the https://wemakeit.com/projects/reseq-reuse-dna-sequencers pages is that
components will be developed for uses first and maybe some day allow open uses, but not really in conflict with Illumina's
patents, and so not using their consumables.  They did not say they were going to make the machines run as they did
when new.

Driving them as an automated microscope was first on the to do list.

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Re: [DIYbio] 3D printer capable of printing autoclavable resin

Biomakespace have been testing some PP 3D prints in our autoclave with some success, there was no difference in integrity up to about 8 cycles (before someone emptied the autoclave without realising the test piece was in there and threw it away!)
There was an increase in what I can only describe as "tackiness" of the material though so you'd want to test that there isn't leaching from the outer layers that could mess with your assay.

We didn't have too much trouble printing with it using our Prusa i3 MK3 and we're planning a more thorough experiment with some tests for strength and deformity. I can find out the filament brand and printer settings from the member who was using it if that helps!

Jenny


On Saturday, 27 April 2019 15:18:06 UTC+1, Dakota Hamill wrote:
Making custom modification pieces to standard lab-ware to make certain assays easier to run.  Basically devices that come into contact with molten agar.  PP looks pretty finicky to print with. Polycarbonate looks easier to work with but will breakdown over repeated cycles and looks sensitive to pH swings?  We had someone print a mold and try to cast resin in it but the resin wasn't getting into all the nooks and crannies of the mold even with degassing it under vacuum.    Thank you for the suggestions will read more into PP as I trust the material, just finding the best printer for it I suppose. Or sucking it up and looking at a Formlabs



On Fri, Apr 26, 2019 at 10:29 PM Abizar Lakdawalla <abi...@gmail.com> wrote:
what are you trying to make? It may be easier to mill or machine polypropylene and polycarbonate. Polypropylene can withstand autoclaving but are difficult to 3D print. Polycarbonate can also withstand autoclaving and is easier to 3D print.

On Fri, Apr 26, 2019 at 6:29 PM Dakota Hamill <dko...@gmail.com> wrote:
Has anyone had any success with either heated extrusion or resin printers to create prints with resins capable of standing repeated autoclave cycles? 







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[DIYbio] How Sea-Monkeys, NovoNutrients, and Synthetic Biology Will Save the World Inc article

https://www.inc.com/magazine/201905/jeff-bercovici/synbio-novonutrients-bioeconomy-sustainable-food-industry-carbon-bioengineering.html

In an office park on a leafy side street in Mountain View, California, a few miles from the headquarters of Google and Facebook, NovoNutrients CEO David Tze is showing off a technology so powerful, it just might avert human civilization from its 200-year collision course with disaster.

Striding past humming electrolyzers separating water molecules into their component elements and liquid chromatographers analyzing the molecular components of samples, he stops before a fluorescent-lighted cylindrical water tank with tiny specks floating in it. "These are the only macroscopic organisms we have here," he says. "These are Artemia."

Artemia salina, that is, a crustacean found in brackish waters and better known by its common name, brine shrimp. If you've heard of brine shrimp, it's likely because, in 1964, a man named Harold von Braunhut began marketing them as a pet-cum-novelty toy under the brand name Sea-Monkeys.

The cutting-edge science I'm looking at is a 55-year-old children's amusement from the back of a comic book?

"Yes," Tze confirms. But, he adds, "we don't give them the official Sea-Monkey feed. They just get our product."

That product is Novomeal, a protein developed for use in aquaculture, and the Sea-Monkeys are proof of concept. Fish food for fish farms, basically. The key ingredient in the commercial feed formulations used in the farming of salmon, tuna, and other carnivorous species prized by consumers is something called fishmeal, a powder made from the ground-up bodies of tiny fish such as anchovies. ("Fishmeal is strangely named: It's meal made from a fish, but it also happens to be an important part of a meal for a fish," Tze says.) Novomeal, a nutritionally complete substitute for fishmeal, is made from the proteins of bacteria and other single-celled organisms, incubated in giant steel vessels akin to beer vats, called bioreactors. Feed is the biggest cost of fish farming, a $232 billion global industry, and, given that the output of the world's overexploited oceans continues to decline, it's only getting more expensive. The supply of bacteria, on the other hand, is effectively infinite, as long as you have the nutrients to feed them.

That part--the nutrients--is why this particular fish food could play such a meaningful role in determining the fate of the planet. What the bacteria that make up Novomeal eat is CO2. You know: carbon dioxide, the stuff that's been building up in the atmosphere since the start of the Industrial Revolution, trapping solar energy and turning the seas acidic. If you believe the U.N.'s Intergovernmental Panel on Climate Change--­or the U.S. Department of Defense, or the big petroleum companies--manmade global warming is a danger on par with no other, threatening to redraw coastlines, spark wars, imperil food and water supplies, alter weather patterns and marine currents, and displace hundreds of millions of people, all within our lifetimes. In the U.S., increasingly severe hurricane and wildfire seasons have already offered a preview of climate change's long-term effects; according to the IPCC, the world's economies must cut their carbon output in half by 2030 to avoid passing a critical threshold beyond which the consequences grow rapidly worse.

"The path to getting out of here," says synbio investor Vijay Pande, "is not as bleak as it may seem."

But if the need to curb carbon emissions is clear, how to do it without torpedoing the world's economy is anything but. Global energy demand is rising fast, and oil, coal, and gas continue to satisfy most of that need. As hundreds of millions of people in China, India, and other developing nations enter the middle class, they're demanding all the perquisites of the Western lifestyle, from hamburgers to new cars. Even if the electricity required to make all that stuff can be obtained from clean renewables, like wind and solar--and we're a long way from that--the production remains a dirty, carbon-intensive business. The plastic that's in everything from yogurt containers to carpet fibers is derived from fossil fuels, typically using energy also derived from fossil fuels. Cows raised for milk and meat have a carbon footprint comparable to that of automobiles. Even something as simple as growing rice can't be done without contributing to warming: Rice farming produces 13 percent of the world's methane, a potent greenhouse gas, because flooding the ground to make paddies brings dormant anaerobic bacteria roaring back to life. As long as more humans are eating more food and buying more stuff, getting a handle on climate change will be fiendishly difficult.

Or not, if David Tze has his say. What his company is constructing--along with others working similar angles in San Francisco and Berkeley and Skokie, Illinois--is nothing less than the infrastructure for an entirely new economy, one premised on producing food, energy, and material goods by sequestering harmful chemicals rather than by emitting them. It's an economy where we'll turn landfill into jet fuel, weave clothing out of spider silk, and make furniture out of mushrooms, all using primarily renewable power. "What we're doing has the potential to change not only the food system," Tze says, "but also the way other goods are manufactured."

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Re: [DIYbio] ReSeq crowd funder to write new software for HiSeq DNA sequencers

This guy is cool.  A lot of people I know in sequencing mention his blog.  (I know next to nothing about NGS).  Maybe he'd give you a shoutout, maybe not. 




On Sat, Apr 27, 2019 at 11:57 AM Kaspar Emanuel <kaspar.emanuel@gmail.com> wrote:
Hi folks,

John is right, the campaign is only for writing software to allow people to drive the machines. You will be able to use the Micromanager interface and scripting capabilities to do whatever you want, including patented procedures, if you can get your hands on the consumables and if you aren't exploiting them commercially, but IANAL, just a software developer.

Looks like this will be a close call as to whether we will reach our funding goal, any suggestions on where else to post are very much appreciated.

Cheers,

Kaspar

On Thursday, April 25, 2019 at 3:05:18 PM UTC, John Griessen wrote:
On 4/24/19 10:23 PM, Abizar Lakdawalla wrote:
> any plan on getting the consumables for the HiSeq? They cost US$10ks per run if they are bought from Illumina.

My take on reading the https://wemakeit.com/projects/reseq-reuse-dna-sequencers pages is that
components will be developed for uses first and maybe some day allow open uses, but not really in conflict with Illumina's
patents, and so not using their consumables.  They did not say they were going to make the machines run as they did
when new.

Driving them as an automated microscope was first on the to do list.

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Re: [DIYbio] ReSeq crowd funder to write new software for HiSeq DNA sequencers

Hi folks,

John is right, the campaign is only for writing software to allow people to drive the machines. You will be able to use the Micromanager interface and scripting capabilities to do whatever you want, including patented procedures, if you can get your hands on the consumables and if you aren't exploiting them commercially, but IANAL, just a software developer.

Looks like this will be a close call as to whether we will reach our funding goal, any suggestions on where else to post are very much appreciated.

Cheers,

Kaspar

On Thursday, April 25, 2019 at 3:05:18 PM UTC, John Griessen wrote:
On 4/24/19 10:23 PM, Abizar Lakdawalla wrote:
> any plan on getting the consumables for the HiSeq? They cost US$10ks per run if they are bought from Illumina.

My take on reading the https://wemakeit.com/projects/reseq-reuse-dna-sequencers pages is that
components will be developed for uses first and maybe some day allow open uses, but not really in conflict with Illumina's
patents, and so not using their consumables.  They did not say they were going to make the machines run as they did
when new.

Driving them as an automated microscope was first on the to do list.

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Re: [DIYbio] 3D printer capable of printing autoclavable resin

Making custom modification pieces to standard lab-ware to make certain assays easier to run.  Basically devices that come into contact with molten agar.  PP looks pretty finicky to print with. Polycarbonate looks easier to work with but will breakdown over repeated cycles and looks sensitive to pH swings?  We had someone print a mold and try to cast resin in it but the resin wasn't getting into all the nooks and crannies of the mold even with degassing it under vacuum.    Thank you for the suggestions will read more into PP as I trust the material, just finding the best printer for it I suppose. Or sucking it up and looking at a Formlabs



On Fri, Apr 26, 2019 at 10:29 PM Abizar Lakdawalla <abizarl@gmail.com> wrote:
what are you trying to make? It may be easier to mill or machine polypropylene and polycarbonate. Polypropylene can withstand autoclaving but are difficult to 3D print. Polycarbonate can also withstand autoclaving and is easier to 3D print.

On Fri, Apr 26, 2019 at 6:29 PM Dakota Hamill <dkotes@gmail.com> wrote:
Has anyone had any success with either heated extrusion or resin printers to create prints with resins capable of standing repeated autoclave cycles? 







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Re: [DIYbio] 3D printer capable of printing autoclavable resin

what are you trying to make? It may be easier to mill or machine polypropylene and polycarbonate. Polypropylene can withstand autoclaving but are difficult to 3D print. Polycarbonate can also withstand autoclaving and is easier to 3D print.

On Fri, Apr 26, 2019 at 6:29 PM Dakota Hamill <dkotes@gmail.com> wrote:
Has anyone had any success with either heated extrusion or resin printers to create prints with resins capable of standing repeated autoclave cycles? 







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[DIYbio] 3D printer capable of printing autoclavable resin

Has anyone had any success with either heated extrusion or resin printers to create prints with resins capable of standing repeated autoclave cycles? 







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[DIYbio] useful chart showing wavelengths for common DNA and protein fluor dyes vs LEDs

This helped quite a bit when I was making LED fluorometers and transilluminators.
Let me know if you need me to add any dyes or have corrections.
Thanks
Abizar

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[DIYbio] Genspace is hiring!

Hi all,

Genspace is hiring! We're looking for a new Lab Manager to begin this summer. Deadline to apply is May 31st.  Please spread the word!

Thank you,
Angela


--
Angela Armendariz, Ph.D.
Biosafety Fellow / Lab Manager

132 32nd Street, Suite 108
Brooklyn, NY 11232
(929) 387 - 8100

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[DIYbio] Fwd: Important Message about the NIH Guidelines

Recent development in the oversight of human gene transfer research...

Forwarding to DIYbio and CSA Ethics lists.

---------- Forwarded message ---------
From: Bayha, Ryan (NIH/OD) [E] <bayhar@od.nih.gov>
Date: Fri, Apr 26, 2019 at 8:56 AM
Subject: Important Message about the NIH Guidelines
To: Bayha, Ryan (NIH/OD) [E] <bayhar@od.nih.gov>


Dear Colleagues:

 

Today, the National Institutes of Health (NIH) finalized a proposal to amend the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules (NIH Guidelines) to streamline the oversight of gene therapy research. This proposal, which was developed in conjunction with the Food and Drug Administration, included amending the NIH Guidelines to eliminate duplicative review and reporting requirements for human gene transfer protocols and refocuses the role of the NIH Recombinant DNA Advisory Committee (RAC) as a transparent forum for science, safety, and ethics of emerging biotechnologies. After a 60-day public comment period, the NIH Guidelines have been updated to reflect these changes and the RAC has been renamed the Novel and Exceptional Technology and Research Advisory Committee (NExTRAC).  

 

Please note that the roles and responsibilities of Institutional Biosafety Committees (IBCs) to review gene therapy protocols have been modified so that they are consistent with the review of other research covered under the NIH Guidelines. Gene therapy protocols remain subject to Food and Drug Administration (FDA) and other clinical trial regulations, and only after FDA, Institutional Biosafety Committee, Institutional Review Boards, and other relevant approvals are in place can these protocols proceed.

 

Please also note the HGTprotocols@od.nih.gov mailbox previously listed in the NIH Guidelines is no longer operational.  All questions should instead be sent to NIHGuidelines@od.nih.gov

 

For more information about these important changes, please see the following NIH resources.

 

 

Ryan T. Bayha

Director of Strategic Engagement

Office of Science Policy

National Institutes of Health

6705 Rockledge Drive, Suite 750

Bethesda, MD 20892

301- 496-9838 (p)

301-496-9838 (f) 

 

     Under the Poliscope Blog                                

             

                                                                                                         

 

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     Follow OSP on LinkedIn    

 

                     

 

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