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7 Dec 2006: A pre-culture, grown in 2¥ TY, was used in a1:1000 dilution to inoculate 200 ml of minimal medium con-taining 1¥ M9 supplemented with 0.4% glucose, 2 mMMgSO4,

30 Nov 2006: Substrate-Specific TranslocationalAttenuation during ER Stress Definesa Pre-Emptive Quality Control PathwaySang-Wook Kang,1,4 Neena S. Rane,1,4 Soo Jung Kim,2 Jennifer L. Garrison,3 Jack Taunton,3. and Ramanujan S. Hegde1,1 Cell Biology and

28 Nov 2006: Acetyl Transferase Assays. GST-MEK2 (0.5 g) (purified by usingstandard protocols for GST-tagged protein purification) wasincubated with varying amounts (0 –200 ng) of (His)6-YopJ-wt ... Stimulation of MEK and Erk phosphorylation by various

12 Nov 2006: Briefly, a 1 ml sample of each PX domain was loaded onto a Superdex 200 column (Amersham-Pharmacia) equilibrated and eluted with 20 mM Tris-HCl buffer, pH 7.4, containing

12 Nov 2006: Further purifi cation was by gel fi ltration on Superdex 200 in 10 mM Tris-Cl, pH 8.0, 0.15 M NaCl, 1 mM DTT, and 1 mM EGTA and

12 Oct 2006: c) Superdex 200 gel filtration of E. coli FtsKg in the presence of DNA. ... Storage buffer was. 20 mM Tris-HCl, 200 mM NaCl, 1 mM EDTA and 1 mM sodium azide.

28 Sep 2006: 50 nm. 100 nm. 200 nm. I. Supplementary Figure 2. The crystal structure of BDLP in GDP-associated and nucleotide-free conformation.

21 Sep 2006: P1: FCG/SPH P2: FCG. SVUS002-Brown November 23, 2004 21:25. Chapter 16. THE MOLECULAR BASIS OF PRIONPROTEIN-MEDIATED NEURONAL DAMAGE. Ramanujan S. Hegde and Neena S. Rane. Cell Biology and Metabolism Branch, NICHD,National Institutes of Health,

8 Sep 2006: cold stage in a Philips Tecnai F20 electron microscope operating. at 200 kV.

12 Aug 2006: agent (200 ml in 700 ml water) was added and Pi release monitored. ... tios of these proteins were mixed (in buffer A plus 200 mM NaCl;.