BiomolecularInteractionsLeeds

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BiomolecularInteractionsLeeds

BiomolecularInteractionsLeeds

@BindingLeeds

Biomolecular Interactions technology facility at the University of Leeds. SPR, ITC and MST for binding assays. Refeyn for solution molecular weights.

Katılım Ağustos 2021
29 Takip Edilen107 Takipçiler
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University of Leeds
University of Leeds@UniversityLeeds·
Since 2009, we’ve used this account to share University updates, highlight research stories, and connect with the Leeds community far and wide. However, in recent years - like many others - we’ve experienced a huge drop in engagement due to developments on the platform.
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RadfordLab
RadfordLab@RadfordLab·
Are you interested in proteins as exciting, dynamic interacting species. Come and join us!   Places are limited so please register ASAP at sheena-radford-lab.uk/fida.php. (£25.00 registration only, including excellent catering).
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BiomolecularInteractionsLeeds
BiomolecularInteractionsLeeds@BindingLeeds·
Excited to have Neo detectors installed on our Fida this week. Extending the concentration range for size, shape, heterogeneity & aggregation measurements. Kinetics & binding assays also from @FIDATechnology. Thanks Tom & @JoanneWalter4 Many thanks @BBSRC for funding.
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BiomolecularInteractionsLeeds@BindingLeeds·
@calfieri84 This is an idea from the old VP-ITC manual. In the syringe, CaCl2 5mM and in the cell, EDTA 0.4mM. Both in MES buffer 10mM pH 5.6. For our ITC200, 1x 0.5ul injection then 19x 2ul with 2 minute spacing. Reference power set on 5 and temperature 25oC.
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Claudio Alfieri
Claudio Alfieri@calfieri84·
@BindingLeeds Nice! Could I ask you some details about it (concentrations and so on)? I would like to do the same in our machine.
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BiomolecularInteractionsLeeds@BindingLeeds·
Mixed week of binding results, so it's good to finish the week with a positive, to check the machine is working properly - ITC of Ca2+/EDTA binding.
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BBS
BBS@BritBiophysSoc·
Abstract submission for the British Biophysical Society Biennial Meeting 2024 is now open! britishbiophysicss.wixsite.com/swansea2024 Join us for three days of all things Biophysics - and for the first time in Wales! An exciting line-up of speakers, including this year's BBS awardees below:
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BiomolecularInteractionsLeeds@BindingLeeds·
I'm proud of how the facility contributes to some UG and Masters practicals. Very pleased that someone nominated me for one of the Faculty partnership awards - surprised to actually get the award. Couldn't have done it without our facility and teaching lab technical staff.
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BiomolecularInteractionsLeeds@BindingLeeds·
Super sessions at the @FIDATechnology user meeting in Copenhagen, seeing how Fida fits with the biophysics & structural biology tool-kit. Designing better assays workshops. Great talk from @aip_taylor, @RadfordLab, using Fida & other tech to study protein aggregation pathways.
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BiomolecularInteractionsLeeds@BindingLeeds·
Loving the rapid size analysis from Fida 1, before an assay or troubleshooting issues after. A gallery of results. Good - large signal, low aggregation Not great - less signal than expected Oops - aggregation, low signal Thank you for the loan @FIDATechnology @RadfordLab
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BiomolecularInteractionsLeeds@BindingLeeds·
You're gonna need a bigger rack. 122 SPR cycles for small-molecule titrations - 10+ hours run time. Successful week of binding assays using #Biacore
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Fidabio
Fidabio@FIDATechnology·
Dear users, it is time to sing up for Fidabio User Group meeting 2024! Few last speaking slots remain available, so if you want to make sure your research is seen, hurry up: eventbrite.dk/e/3rd-fidabio-…
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BiomolecularInteractionsLeeds@BindingLeeds·
Solution measurements of size & shape. Refeyn mass photometry of M.Wt. - VLPs & proteins (left-hand pics). @refeynit Loving Fida also for smaller & unstructured molecules, aggregation assays, Ex488 & 280nm, automation... V. grateful to @FIDATechnology for the loan. @RadfordLab
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BiomolecularInteractionsLeeds@BindingLeeds·
My last practical session with our Biopharma students today. Including mAb purification & SDS-PAGE. Have you purified a good (enough) reagent? Is one buffer better than another? Enough capacity in 1 column? + & - DTT (2 images of each) Thank you students - it's been good.
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