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1 - 10 of 29 search results for KaKaoTalk:vb20 200 |u:www-jackson.ch.cam.ac.uk where 0 match all words and 29 match some words.

  1. Results that match 1 of 2 words

  2. Protein denaturation and protein:drugs interactions from intrinsic…

    www-jackson.ch.cam.ac.uk/publications/2010/2010_Prot_Sci%20_Gaudet.pdf
    26 Jul 2010: 200 lm laser spot and 1 kHz laser pulsing. Photo-bleaching was only observed at flowrates up to 1 lLmin1 (see Supporting Information Fig. ... Crystalaser, Reno, NV) emitted a 200 lm diameterband-pass filtered (BG3, Newport) ray perpendicular.

  3. doi:10.1016/j.jmb.2004.05.007

    www-jackson.ch.cam.ac.uk/publications/2004/2004_JMB_Hsp90_Zhang_et_al.pdf
    23 Aug 2004: 2: A280 0.3 at (X) 13,200 rpm, (B) 14,500 rpm, (V)16,000 rpm, and (O) 18,700 rpm. ... the Hsp90–Cdc37 complex on an analytical Superdex 200 PC 3.2/30 gel filtration column at 4 8C.

  4. No Job Name

    www-jackson.ch.cam.ac.uk/publications/2002/2002_JACS.pdf
    15 Sep 2003: Folding and unfolding rate constants in water areapproximately 150-200 s-1 and 0.005-0.06 s-1, respectively, at neutral pH and 10 C. ... Mol. Biol. 1996, 256, 187-200.(27) Kragelund, B. B.; Osmark, P.; Neergaard, T.

  5. No Job Name

    www-jackson.ch.cam.ac.uk/publications/2003/2003_Biochem.pdf
    11 Sep 2003: A. (2001) Mutationsin the Cardiac Ryanodine Receptor Gene (hRYR2) UnderlieCatecholaminergic Polymorphic Ventricular Tachycardia,Circula-tion 103, 196-200.

  6. Stimulation of the Weak ATPase Activity of Human Hsp90 by a Client…

    www-jackson.ch.cam.ac.uk/publications/2002/2002_jmb.pdf
    15 Sep 2003: Using a phys-iological substrate of Hsp90, the ligand-binding domain of the glucocorti-coid receptor, we show that this client'' protein can stimulate theATPase activity up to 200-fold. ... We show that a client protein canstimulate the ATPase activity

  7. doi:10.1016/j.str.2006.11.007

    www-jackson.ch.cam.ac.uk/publications/2007/2007_structure_YibK.pdf
    8 Feb 2008: 225 nm. Conditions: 25C in 50 mM Tris-HCl. (pH 7.5), 200 mM KCl, 10% (v/v) glycerol,. ... 200 mM KCl, 10 % glycerol (v/v), 1 mM DTT, except for the ITC exper-.

  8. doi:10.1016/j.jmb.2006.04.032

    www-jackson.ch.cam.ac.uk/publications/2006/2006_Mallam_JMB_YibK.pdf
    4 Jul 2006: using fluorescence at pH 5.5 and pH 4.5 over a 400-fold and a 200-fold change in protein concentration,respectively. ... Unfolding traces areshown after (c) 200 ms refolding delay, (d) 5 s refoldingdelay and (e) 20 s refolding delay.

  9. MR-nsmb1204.indd

    www-jackson.ch.cam.ac.uk/publications/2004/2004_NSMB_Hsp90_report.pdf
    6 Jan 2005: D.T. is in the Department of Biochemistry and Molecular Biology, Mayo Clinic, College of Medicine, 200 First Street SW, Rochester, Minnesota 55905, USA.e-mail: sej13@cam.ac.uk,

  10. doi:10.1016/j.molcel.2008.03.019

    www-jackson.ch.cam.ac.uk/publications/2008/2008_Mol_Cell_Knotted_Fusions.pdf
    1 Aug 2008: from the amino terminus, as the threading of an Escherichia. coli ribosome (approximately 200 Å in diameter [Schuwirth. ... 50 mM Tris-HCl (pH 7.5), 200 mM KCl, 10 % (v/v) glycerol, and 1 mM DTT at.

  11. Chapter 3 - Use of Protein Engineering Techniques to Elucidate…

    www-jackson.ch.cam.ac.uk/publications/2008/2008_Prog_Nuc_Acid_Mol_Biol_Folding_review.pdf
    6 Jan 2009: Provided for non-commercial research and educational use only. Not for reproduction, distribution or commercial use. This chapter was originally published in the book Progress in Molecular Biology and Translational Science, Vol. 84, published by

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