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Arsalan Daudi University of California
153 protocols

Aswad Khadilkar UNIVERSITY OF CALIFORNIA SANTA CRUZ
3 protocols

Cristina Rohena University of California, San Francisco
1 protocol

Dennis Nürnberg Imperial College London
31 protocols

Reviewer
Vikash Verma
  • Research associate, University of Massachusetts
Research focus
  • Cell biology
  • Mitosis, Cytokinesis, Kinetochore, Chromosome Dynamics, DNA Origami

Education

Ph.D., Friedrich Miescher Laboratory of the Max Planck Society

Publications

I. Kulemzina, K. Ang, J.T. Teh, X. Zhao, V. Verma, S. Suranthran, A. P. Chavda, R. G. Huber, B. Eisenhaber, F. Eisenhaber, J. Yen, and D. Ivanov. “A reversible association between Smc coiled coils is regulated by lysine acetylation and is required for cohesin loading on the DNA.” Molecular Cell, 15, 1044-54, (2016).

V. Verma, L. Mallik, R. F. Hariadi, S. Sivaramakrishnan, G. Skiniotis, and A. P. Joglekar. “Maximizing protein hybridization efficiency on multisite DNA origami scaffolds using protein dimerization.” PLoS One, 10(9): e0137125, (2015).

I. Kulemzina, M. Schumacher, V. Verma, J. Reiter, J. Metzler, A. V. Failla, C. Lanza, V. T. Sreedharan, G. Rätsch, and D. Ivanov. ‘‘Cohesin rings devoid of Scc3 and Pds5 maintain their stable association with the DNA.’’ PLoS Genetics, 8(8): e1002856, (2012).

A. Maheshwari, V. K. Verma*, and T. K. Chaudhuri. “Equilibrium and kinetics of the unfolding and refolding of Escherichia coli Malate Synthase G monitored by circular dichroism and fluorescence spectroscopy.” Biochimie, 92, 491-498, (2010).
*Equal contribution

T. K. Chaudhuri V. K. Verma and A. Maheshwari. “GroEL assisted folding of large polypeptide substrates in Escherichia coli: Present scenario and assignments for the future.’’
Progress in Biophysics and Molecular Biology, 99, 42-50, (2009).

7 Protocols reviewed
Characterising Maturation of GFP and mCherry of Genomically Integrated Fusions in Saccharomyces cerevisiae
Authors:  Sviatlana Shashkova, Adam JM Wollman, Stefan Hohmann and Mark C Leake, date: 01/20/2018, view: 131, Q&A: 0
Single-molecule fluorescence microscopy enables unrivaled sub-cellular quantitation of genomically encoded fusions of native proteins with fluorescent protein reporters. Fluorescent proteins must undergo in vivo maturation after expression ...
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Detection of Protein Interactions in the Cytoplasm and Periplasm of Escherichia coli by Förster Resonance Energy Transfer
This protocol was developed to qualitatively and quantitatively detect protein-protein interactions in Escherichia coli by Förster Resonance Energy Transfer (FRET). The described assay allows for the previously impossible in vivo ...
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