enzymaticsynthesis

By 'enzyme' you mean the ribosome? Assembling a functioning ribosome recombinantly is just

Hi all, Over the past few years, there have been a number of interesting proposals to use ligation

---------- Forwarded message --------- From: fenn <fenn...@gmail.com> Date: Sat, Nov 19, 2022

Hi all, My coinventors and I did some work on "promiscuous templates" and "promiscuous

Two publications of recent interest: "De novo DNA synthesis using polymerase-nucleotide

Is there any news? Somebody was conducting new experiments with TdT?

Ok, I could see the nuclease approach working with some protein engineering. Mung bean nuclease is

Interesting ideas. I really like the encoded DNA step, because it allows for new and different ways

Suppose we were stuck with modern DNA synthesis technology. Giant arrays of millions of elements that

On Sat, Sep 17, 2016 at 1:28 PM, Kent Kemmish <kemmi...@gmail.com> wrote: This idea

Quite a back story to share about this one if you like, PM me? On Sunday, July 17, 2016 at 11:32:22

My perspective is that a controlled polymerase is useful regardless of whether it makes DNA or RNA.

How much time was required? 10 minutes or an hour? Why is this happening? PCR using the same 3'-

I wonder if a polymerase changes color while adding nucleotides. Maybe Raman spectroscopy or

Some of the DNA alternatives like XNA and GNA offer some interesting options. Perhaps it would be

On Thu, Dec 25, 2014 at 2:51 PM, Bryan Bishop <kan...@gmail.com> wrote: Similar to using TdT

Here is a broadly applicable concept: Enzymatic protecting group techniques (2001) http://www.kois.sk

On Aug 23, 2012 9:51 PM, "Jonathan Cline" <jnc...@gmail.com> wrote: > > There

On Wed, Jun 13, 2012 at 12:41 AM, Jonathan Cline <jnc...@gmail.com> wrote: Kettner Griswold (

On Sat, May 5, 2012 at 2:13 PM, Jonathan Cline <jnc...@gmail.com> wrote: Why avoid mistakes?

rOn Wednesday, February 29, 2012 12:36:37 AM UTC-5, Nathan McCorkle wrote: If you could make a

aaand #6. Essentially, what the research boiled down to is some study into the minimum template/

On Fri, Feb 24, 2012 at 7:18 PM, Bryan Bishop wrote: > using light to dissociate the complex; you

I recently attended a conference where Dr. Duhee Bang talked about a method of relatively long DNA

Here's a simple start to a document that we can hopefully fill out as we go along. Anyone is

On Tue, Feb 21, 2012 at 3:25 AM, Cory Tobin wrote: [Off topic] Was this a Breakout Labs proposal? I

> i think terminal transferase and optogenetics are the best place to > start... engineer one

Here is my brain storm after reading some of the above.... 1000 bp per second / 3000000000 bp =