The largest database of trusted experimental protocols

Isv 922

Manufactured by Jasco
Sourced in Japan

The ISV-922 is a laboratory instrument designed for conducting various scientific experiments and analyses. It is a versatile piece of equipment that can be used in a wide range of research and testing applications. The core function of the ISV-922 is to provide accurate and reliable data measurements and analysis capabilities to support scientific investigations. Further details on its intended use or specific applications are not available.

Automatically generated - may contain errors

5 protocols using isv 922

1

Leaf Optical Property Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
A spectrophotometer (V-750, JASCO Corporation, Tokyo, Japan) was used to measure the reflection and transmission spectra (Gausman and Allen, 1973 (link); Saito et al., 2020 (link)) of the first leaf from the top of the main stem (fully expanded and unshaded leaf) at 82 DAS of the plant with an integrating sphere unit (ISV-922, JASCO Corporation, Tokyo, Japan). The measured light spectrum ranged from 400 to 700 nm. Three or four plants without fruit pruning were sampled per treatment. For each wavelength, the absorptance was calculated as 100% minus reflectance and transmittance.
+ Open protocol
+ Expand
2

Leaf Optical Properties and Chlorophyll Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The reflection and transmission spectra of the third leaf (fully expanded and unshaded leaf) from the top of the plant were measured using a spectrophotometer (V-750, JASCO Corporation, Tokyo, Japan) with an integrating sphere unit (ISV-922, JASCO Corporation, Tokyo, Japan) at 10 DAT. The range of the measured light spectrum was 400–700 nm. Eight and four plants in each treatment in Experiments 1 and 2 were sampled, respectively. Absorptance was calculated for each wavelength as follows:
Chlorophyll pigment was extracted from the third leaf from the top of the plant with N,N-dimethylformamide at 10 DAT, according to the protocol described by Porra et al. [81 (link)]. For chlorophyll concentration analysis, four leaves from four plants in each treatment were sampled. The chlorophyll concentration was determined on a dry weight basis by measuring the absorbance of the leaf extracts at 663.8, 646.8, and 750.0 nm using an ultraviolet-visible spectrophotometer (V-750, JASCO Corporation, Tokyo, Japan).
+ Open protocol
+ Expand
3

Structural and Surface Analysis of TNAs

Check if the same lab product or an alternative is used in the 5 most similar protocols
The crystal structure of TNAs and Fe/TNAs was investigated by X-ray diffraction (XRD) (X’Pert Pro MRD, PANalytical, Almelo, The Netherlands) using a Cu Kα source at a wavelength of 0.154 nm. JCPDS PDF card database was selected as the identification of XRD peaks. The morphology was studied using a field-emission scanning electron microscope (Nova NanoSEM 430 FEI, Hillsboro, OR, USA). The specific surface area of TNAs and Fe/TNAs were measured by BET (ASAP 2020 N (S/N: 1195), Micromeritics, Norcross, GA, USA) analysis under 740 mmHg of pressure (P0) and 77.350 K of bath temperature. Raman analysis was conducted by using 532 nm Laser, with 1800 cm−1 grating and 50 s exposure time, operating by Labspec5 software. The X-ray photoelectron spectroscopy (XPS) experiments were conducted on the TNAs and Fe/TNAs using a PHI 5000 Versa Probe system (Physical Electronics, Chanhassen, MN, USA). The binding energy that was obtained from the XPS spectra was calibrated with reference to the C1s peak at 284.8 eV. The UV-vis absorption spectra were measured in diffused reflection mode using an integrating sphere (ISV-922, Jasco, Tokyo, Japan) that was attached to a Jasco V-750 UV-vis DRS spectrometer (V-750, Jasco, Tokyo, Japan).
+ Open protocol
+ Expand
4

Rhodopsin Spectral Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The λmax values of the WT and mutants of SzR4, SzR2, and SzR3 were determined by bleaching the protein with HA, according to the previously reported method (30 (link)). E. coli cells expressing rhodopsins were washed three times with buffer containing 50 mM Na2HPO4 (pH 7.0) and 100 mM NaCl. The washed cells were treated with 1 mM lysozyme for 1 h at room temperature and then disrupted by sonication. To solubilize the rhodopsins, 3% DDM was added and the samples were stirred overnight at 4 °C. The rhodopsins were bleached with 500 mM HA in the dark or under yellow light illumination (λ > 500 nm) from the output of a 1 kW tungsten halogen projector lamp (Master HILUX-HR, Rikagaku) passed through a glass filter (Y-52, AGC Techno Glass). The absorption change upon bleaching was measured by a UV-visible spectrometer (V-730, JASCO) equipped with an integrating sphere (ISV-922, JASCO).
+ Open protocol
+ Expand
5

Spectroscopic Characterization of Rhodopsin Mutants

Check if the same lab product or an alternative is used in the 5 most similar protocols
The λmax values of the wildtype and mutants of SzR4, SzR2, and SzR3 were determined by bleaching the protein with hydroxylamine, according to the previously reported method 22 . E. coli cells expressing rhodopsins were washed three times with buffer, containing 50 mM Na2HPO4 (pH 7) and containing 100 mM NaCl. The washed cells were treated with 1 mM lysozyme for 1 hr at room temperature, and then disrupted by sonication. To solubilize the rhodopsins, 3% DDM was added and the samples were stirred overnight at 4 °C. The rhodopsins were bleached with 500 mM hydroxylamine in the dark or under yellow light illumination (λ > 500 nm) from the output of a 1 kW tungsten-halogen projector lamp (Master HILUX-HR, Rikagaku) passed through a glass filter (Y-52, AGC Techno Glass). The absorption change upon bleaching was measured by a UV-visible spectrometer (V-730, JASCO, Japan) equipped with an integrating sphere (ISV-922, JASCO, Japan).
+ 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!