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AFFINITY SCREENING
Dianthus overview
Monolith NT.Automated overview
Screening analysis software
BINDING AFFINITY
Monolith overview
Control software
Monolith for challenging targets
Monolith consumables
PROTEIN STABILITY + AGGREGATION + PARTICLE SIZING
Prometheus overview
Stability analysis software
Prometheus for biologics ✨
PROTEIN QUALITY
Tycho overview
Tycho for SPR
Get to know Tycho
Tycho purchase packages
THERAPEUTIC AREAS
PROTACs
Characterize binary and ternary complexes
Gene Therapy
Develop safe and effective gene therapies
DISEASES
Neurodegenerative Diseases
Overcome ND research challenges
TARGETS
Membrane Proteins
Characterize in solution with any buffer or detergent
RESEARCH AREAS
Plant Science
Improve your plant science research
Virology
Unravel virus biology complexity
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TOOLS FOR USERS
Protein labeling assistant
Find the best protein labeling strategy
Degree-of-labeling calculator
Calculate your DOL when labeling proteins
Dianthus assay development assistant
Get guidance on TRIC assay development
NANOPEDIA
Dianthus NanoPedia
Find knowledge articles related to Dianthus
USER TRAININGS
Online Basic Monolith User Trainings - Europe
Take part in training on measuring binding affinity
Online Advanced Monolith User Trainings - Europe
Get customized training on binding affinity measurements
Prometheus User Trainings - Germany
Join training to learn about protein stability
Basic Monolith User Trainings - USA
Join training on measuring binding affinity
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Know #proteinqualityfirst
Coming January 8
Curious?
Does this ever happen to you?
Choose...
I accidentally left my sample out on my bench and I'm not sure if it's still good 🙁
I hope the aliquots I put in the -80 °C freezer are okay.
I got samples from my colleague but for some reason they aren't working the way they should.
I guess today will end up being a gel-running day checking all these column fractions.
But I followed the protocol to the T and still got crappy results!
I can't tell if it's the salt or pH of the buffer that's killing my sample.
You: Sample, please tell me if you're going to treat me right or cause me trouble. Sample: Nope.
I have a feeling that my prep today isn't going to work as well as the previous one I used.
I really wish I didn't have to test such a large matrix of conditions to optimize my assay.
The results I got are pretty similar. Should I run it again...?
It's going to be another late evening in the lab, I'm starting that protein purification...
You're not the only one who's ever done that before! No worries, there's a way to find out if you should invest more time working with that sample.
Sign up to be one of the first to learn about T _ _ _ o before it officially launches on January 8.
I want to sign up
There's always a possibility that your samples, whether stored long term or overnight, function as you expect or if they had been freshly made. If you want to test storage conditions beforehand or be confident your samples will work prior to spending your entire day at the bench with them, sign up below.
You'll be one of the first to learn about T _ _ _ o before it officially launches on January 8.
I want to sign up
We've all been there. Think you're saving some time by using someone else's prep.....Well surprise, you're spending more time troubleshooting your assay.
Sign up to learn about T _ _ _ o before it launches on January 8 and just make sure that sample prep is okay before you embark on those experiments.
I want to sign up
It's already so much work running columns and collecting fractions, and now you have to run multiple gels to check if your sample is even there. Wouldn't it be nice to quickly screen your samples instead?
Sign up to be one of the first to learn about T _ _ _ o before it launches on January 8 and say
see ya
to gels.
I want to sign up
We hear ya. It gets pretty frustrating when you follow every step of a protocol, spend all that time and effort, and your experiment still doesn't work. Want to learn how to troubleshoot your protocols more effectively?
Sign up below to find out about T _ __o before it launches on January 8, and be known as the person who makes experiments work every time.
I want to sign up
Proteins can be so finicky. Sometimes it's just that one thing in your buffer that kills the activity of your sample. How awesome would it be to identify what that thing is before you invest all that time doing experiments.
Sign up to be one of the first to learn about T _ _ _ o before it officially launches on January 8.
I want to sign up
Unfortunately, your samples won't speak to you.
Sign up to be one of the first to learn about T _ _ _o before it launches on January 8 and make your samples join the conversation.
I want to sign up
What it sounds like is that you need a way to figure out if your samples are similar.
Sign up to be one of the first to learn about T _ _ _ o before it officially launches on January 8 and give yourself a little pat on the back for being so consistent.
I want to sign up
Matrices are great when it comes to tracking of all your testing conditions, but isn't so fun when it comes time to set up and run them.
Sign up to be one of the first to learn about T _ _ _ o before it is officially introduced on January 8 and maybe you won't mind running those matrix experiments so much.
I want to sign up
Ummm...run it again, spend extra time and break the tie or... sign up to find out about T _ _ _ o before it launches on January 8.
I want to sign up
It doesn't have to be another long night. You can find out early on if your experiments are a go.
Sign up to learn about T _ _ _ o before it launches on January 8 and get home to binge watch that Netflix show everyone's talking about!
I want to sign up
Be the first to know about T_ _ _o!
Sign up to learn more right before we launch
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