Diego Wengier 1 protocol

M. Anleu Gil Department of Biology, Stanford University, USA, USA,
1 protocol
Imre Gáspár INSTITUTE OF MOLECULAR BIOTECHNOLOGY, IMBA, Vienna
21 protocols

Julie Weidner AstraZeneca
9 protocols

Shalini Low-Nam Purdue University
14 protocols

Reviewer
Nidhi Sharma
  • HHMI/Stanford University
Research focus
  • Plant science
  • 2 Author merit

Education

Ph.D., The University of Texas at Austin, USA, 2011

Current position

Research Specialist/Lab Manager, Biology, Stanford University/HHMI, United States

Publications

  1. Sharma, N. and Barton, M. K. A novel epistatic mechanism between SHOOTMERISTEMLESS and CLAVATA genes in regulating stem cell population at Shoot Apical Meristem. (Manuscript in preparation).
  2. Magnani, E.,  Longhurst, A., Cabalona, L., Sharma, N., Reinhart, B. J., Liu, T., Talavera-Rauh, F., Huang, T., Hokin, S. A., Kerstetter, R. A. and Barton, M. K. The Abscisic Acid Signaling Pathway and the Ad/Abaxial Developmental Pathway Interact to Regulate Germination and Vegetative Growth in Arabidopsis. (In review).
  3. Sharma, N., Xin, R., Kim, D. H., Sung, S., Lange, T. and Huq, E. (2016). NO FLOWERING IN SHORT DAY (NFL) is a bHLH transcription factor that promotes flowering specifically under short-day conditions in Arabidopsis. Development 143(4): 682-690.
  4. Sharma, N. and Huq, E. (2011). Identification and functional characterization of target genes for NFL. 6:32493.
2 Protocols published
一种使用氯化铷快捷简易制备进行细胞转化的大肠埃希杆菌感受态的方法
Authors:  Nidhi Sharma, M. Ximena Anleu Gil and Diego Wengier, date: 11/05/2017, view: 16887, Q&A: 2
This protocol describes a quick and efficient method to make competent E. coli cells for transformation using rubidium chloride. Commercial competent cells are expensive and this protocol provides a cheaper alternative to them.
用于观察叶面气孔和其他细胞的叶片透化方案
Author:  Nidhi Sharma, date: 09/05/2017, view: 14717, Q&A: 1
In this protocol, leaves are cleared and fixed in an ethanol and acetic acid solution, and mounted in Hoyer’s solution. The cleared leaves are imaged under differential interference contrast (DIC) microscope. This protocol is beneficial for studying ...
3 Protocols reviewed
Comprehensive Identification of Translatable Circular RNAs Using Polysome Profiling
Authors:  Yanwen Ye, Zefeng Wang and Yun Yang, date: 09/20/2021, view: 516, Q&A: 0

Circular RNAs (circRNAs), a special type of RNAs without 5’- and 3’-ends, are widely present in eukaryotes and known to function as noncoding RNAs to regulate gene expression, including as miRNA sponges. Recent studies showed that many

...
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Detection of Individual RNA in Fixed Cells and Tissues by Chromogenic ISH
Authors:  Meng Jiang, Chen Lin and Rongqin Ke, date: 02/05/2020, view: 2398, Q&A: 0
Visualization of RNA molecules in situ helps to better understand the functions of expressed genes. Currently, most conventional in situ hybridization methods for visualization of individual RNAs are based on fluorescence ...
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