The largest database of trusted experimental protocols

Winrhizo pro2003b

Manufactured by Regent Instruments
Sourced in Canada

WinRHIZO Pro2003b is a software package for the analysis of root systems. It provides tools for the measurement and quantification of various root system parameters, such as root length, root surface area, and root volume, from digitized root samples.

Automatically generated - may contain errors

5 protocols using winrhizo pro2003b

1

Comprehensive Root Morphology Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
For the analysis of root morphology, the whole root system of the same plants used for the collection of exudates was scanned using the WinRHIZOTM system (WinRhizo software, EPSON 1680, WinRHIZO Pro2003b, Regent Instruments Inc., Quebec, QC, Canada). The dry weight of shoots and roots was recorded after drying at 65 °C until constant mass.
+ Open protocol
+ Expand
2

Root Morphological Trait Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
After root exudate collection, the sampled all roots were clipped from the tree, scanned at 400 dpi, and analyzed with a WinRhizo™ Pro 2003b image analysis system (Regent Instruments Inc., Ville de Québec, QC, Canada) to establish diameter, length, and projected area. Air-dried roots were further desiccated at 70 °C for 24 h to constant weight and then weighed. Root tissue density (RTD; kg m−3), SRA (m2 kg−1), and SRL (m g−1) were subsequently calculated as described by Ostonen et al.19 (link). Root branching intensity was expressed as the number of root tips per 1 mg of dry mass.
+ Open protocol
+ Expand
3

Analyzing Plant Growth and Biomass

Check if the same lab product or an alternative is used in the 5 most similar protocols
Plants were harvested 28 days after transfer to hydroponics, and roots and shoots
were sampled separately for subsequent analysis. The total number of green leaves and
senesced leaves was recorded. Root length and root surface area were measured using
WinRHIZO (EPSON 1680, WinRHIZO Pro2003b, Regent Instruments Inc., Quebec, Canada).
Shoot and root dry weight (DW) were measured separately after being oven-dried for 48
h at 65 °C.
+ Open protocol
+ Expand
4

Root Morphology and Copper Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
At harvest, root morphology parameters (total root length, number of tips, root volume, and average root diameter) were determined using the Winrhizo software (EPSON1680, WinRHIZO Pro2003b, Regent Instruments Inc., Quebec, Canada). Afterward, the roots and leaves were separated and dried at 65°C until constant weight was reached, a portion of the root apparatus was frozen in liquid nitrogen and kept at −80°C for gene expression analysis. Roots and leaves tissues were acid digested (HNO3 65% v/v) in a single digestion chamber (SRC) microwave digestion system (UltraWAVE, Milestone, Shelton, CT, United States) and the Cu concentration was determined by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES, Arcos Ametek Spectro, Germany).
+ Open protocol
+ Expand
5

Phytotoxicity of Alkaloid Metabolites on Lettuce

Check if the same lab product or an alternative is used in the 5 most similar protocols
The phytotoxicity potential of the three metabolites, gramine, hordenine and N-methyltyramine was investigated by measuring the main growth root parameters of lettuce (Lactuca sativa L.) once treated with the three alkaloids. Seeds of lettuce were placed in petri dishes laid out with filter paper (Whatman N°41, Whatman, Maidstone, UK) and soaked with 1 mL of solution of each alkaloid. The solutions were previously prepared from 5 mM MES buffer in distilled water adjusted to pH 6.15 by adding NaOH as described in [49 (link)], in which gramine, hordenine and N-methyltyramine were added in order to reach concentrations of 0.5 mM and 1 mM, obtaining different treatments. Controls were also prepared using the buffer alone. Petri dishes were sealed with Parafilm and incubated in the dark in the climate chamber for 48 hours. Thereafter, the germinated seeds were counted, and the main growth parameters were measured to calculate the inhibition percentage of the three metabolites investigated on Lactuca sativa L.. Root parameters were assessed by scanning the seedlings with WinRHIZOTM system (WinRhizo software, EPSON1680, WinRHIZO Pro2003b, Regent Instruments Inc., Quebec, Canada).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!