Ultra-Pure Genomic Enzymes | CRISPR Enzymes | CLīM Tech
Birmingham, Alabama, USA
Joined March 2018
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Why struggle with messy preps when you could have ultra-pure enzymes on demand? Science smarter, not harder. 🧪✨ trialtusbioscience.com/
Guess who’s back? 👀 After some time away, TriAltus is back on X—now fully focused on high-purity genomic enzymes! Whether you need enzymes for gene editing, gene synthesis or custom production, we’ve got you covered. Let’s talk science. 🔬⚡ #Biotech #Enzymes #MolecularBiology
TriAltus now offers two varieties of #Im7 affinity resin for use with the #CL7 tag system. This blog post covers how to choose the right resin, 4B or 6B, for your #ProteinPurification needs.
trialtusbioscience.com/blogs…
We'll share more detailed data once it's available, but in the meantime here's a blog post that gives an overview of Gentle Elution Buffer's use in eluting tagged protein: trialtusbioscience.com/blogs…
If you want tag-free protein, we still highly recommend proteolytic elution since the tag could have an impact on activity.
Gentle elution buffer is meant more as a replacement for denaturants like guanidine rather than protease, since the eluted protein will still be fused to the CL7 tag. It's easier to use for the resin regeneration step since it won't denature the Im7 ligand!
Thanks for the shoutout, Cody!
If you aren't using the CL7 tag for pull-downs or purifications you're missing out! The 21st century tag is legit and the resin that binds it can be reused 100's of times without losing affinity. S/O @TriAltusBio team for its tag-changing technology.
#FLAG is well-known as an effective epitope tag for isolating high-purity protein. But how does it stack up to #CL7? Read about how the two tag systems compare in this week's blog post: ow.ly/Z7ry50DcKvI
#TriAltusBioscience
Take a look at TriAltus' top-read blog posts from 2020! From #CRISPR to tips for optimizing #ProteinPurification under different conditions, there's something for everyone to learn.
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Did you know that #GentleElutionBuffer can be used to elute proteins without denaturing effects? TriAltus now offers Gentle Elution Buffer as a part of our #ProteinPurification Starter Kit and as a standalone product.
ow.ly/7FSg50CER4O
Why is #endotoxin testing important for purified proteins? Find out in our most recent blog post and learn about the different methods being used like #LAL and #rFC ow.ly/8d4C50CAM9G
Thanks for sharing, Mark!
Sometimes #protein purification hits a roadblock and you have to move out of E. coli. Our preliminary evaluation suggests that this #CL7/Im7 system from @TriAltusBio could solve some problems.
Gentle Elution Buffer is a useful alternative to proteolytic or denaturant elution. Read on the blog how this solution is compatible with the #CL7Im7 system: ow.ly/nFuB50CnbvA
This week's blog post covers another popular #ProteinPurification tag system - #Streptag. Read more here about the system and how it stacks up to #CL7 here: ow.ly/ypkx50CaCHL
This week's blog post covers our newest #RecombinantProtein product: Human Growth Hormone (#hGH). Learn how TriAltus used the CL7/Im7 system to ensure ultra-high purity in just a single #chromatography step.
bit.ly/31cspK8
Human Growth Hormone is our latest addition to our purified #RecombinantProtein offerings. Purified with our novel #CL7Im7 system, it achieves >99% purity after only one chromatography step. Learn more on the product listing:
bit.ly/3kU3rqN
Nucleus Biotech is now an official distributor of TriAltus Bioscience products! They will supply our #ProteinPurification consumables, #Proteases, and #RecombinantProteins to consumers in Austria, Germany, and Switzerland.
hubs.ly/H0tFDL70
There are many #AffinityChromatography systems for #ProteinPurification out there, but which one is right for you? This blog post covers two of the most popular tags #His-tag and #FLAG.
TriAltus: Protein Purification Simplified.
hubs.ly/H0sNhHr0
The efficiency of a #CRISPR experiment depends on how well the #Cas protein and gRNA are delivered into the nucleus. This blog post outlines the three main methods for assembling and delivering the CasRNP to cells for editing.
hubs.ly/H0s5CBT0