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A peer-reviewed protocol journal. No publication fee; no access fee.
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Coauthors
Günter Theißen
Department of Genetics, Friedrich Schiller University Jena, Germany
3 protocols
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Coreviewers
Arsalan Daudi
University of California
157 protocols
Joern Klinkenberg
-
2 protocols
Tie Liu
University of Florida
158 protocols
Zhaohui Liu
North Dakota State University
49 protocols
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Reviewer
Teresa Lenser
University of Jena
Research focus
Plant science
Contributions
2
Author merit
Reviewer merit
Editor merit
2 Protocols published
Floral Dip Transformation in
Lepidium campestre
Authors:
Teresa Lenser
and
Günter Theißen
,
date:
08/05/2014,
view:
5331,
Q&A:
0
Floral dip is a very common technique to stably transform
Arabidopsis thaliana
(Clough and Bent, 1998; Martinez-Trujillo
et al.
, 2004; Zhang
et al.
, 2006) and has also been adapted to some other plant species (Curtis and ...
More >
Quantifying Fruit Dehiscence Using the Random Impact Test (RIT)
Authors:
Teresa Lenser
and
Günter Theißen
,
date:
08/05/2014,
view:
4631,
Q&A:
0
Fruit dehiscence is an important evolutionary and agronomic trait. For quantifying and comparing the exact fruit dehiscence capability between individual plants, the random impact test has been described (Morgan
et al.
, 1998; Bruce
et al.
...
More >
6 Protocols reviewed
PEA-CLARITY: Three Dimensional (3D) Molecular Imaging of Whole Plant Organs
Authors:
William M. Palmer
,
Antony P. Martin
,
Jamie R. Flynn
,
Stephanie Reed
,
Rosemary White
,
Robert T. Furbank
and
Christopher P. L Grof
,
date:
11/05/2016,
view:
3206,
Q&A:
0
Here we report the adaptation of the CLARITY technique to plant tissues with addition of enzymatic degradation to improve optical clearing and facilitate antibody probe penetration. Plant-Enzyme-Assisted (PEA)-CLARITY, has allowed deep optical ...
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Agrobacterium rhizogenes
-Based Transformation of Soybean Roots to Form Composite Plants
Authors:
Benjamin F. Matthews
and
Reham M. Youssef
,
date:
01/20/2016,
view:
4566,
Q&A:
0
Transgenic soybean roots of composite plants are a powerful tool to rapidly test the function of genes and activity of gene promoters. No tissue culture is needed, thus avoiding loss of valuable material due to contamination. This is a simple ...
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