The largest database of trusted experimental protocols

Nanolog

Manufactured by Horiba
Sourced in Japan

The NanoLog is a high-performance nanoparticle characterization system developed by Horiba. It is designed to provide accurate and reliable measurements of particle size, size distribution, and other physical properties of nanomaterials. The NanoLog utilizes advanced optical techniques to analyze samples and deliver comprehensive data on the analyzed samples.

Automatically generated - may contain errors

9 protocols using nanolog

1

Thermal Microscopy Device for Cell Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
To heat the cells for ILN testing, an insulated thermal microscopy device was engineered in house using commercially purchased Peltier thermoelectric modules (TE Technology, Inc., Traverse City, MI, USA). The modules were fastened to a customized copper plate in acrylic housing, with a K-type thermocouple. Cover slips seeded with cells were placed onto the plates of the device allowing cell sample heating/cooling (Figure S1). A tunable DC power supply was used to apply potential to the thermoelectrical modules to control heating of the system. For bulk measurements, a similar thermoelectric device was constructed allowing the variation of temperature of the cuvette inside the spectrophotometer (Cary 60 UV-Vis, Agilent, Santa Clara, CA, USA) and spectrofluorometer (Nanolog, HORIBA Scientific, Edison, NJ, USA).
+ Open protocol
+ Expand
2

Hyperspectral Imaging System for Skin Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The imaging HSI push broom data system (Figure 1) featured an SWIR sensitive 2D InGaAs thermoelectrically cooled CCD camera (Ninox, Raptor), a 25 mm focal length SWIR lens (StingRay Optics), an imaging spectrograph Imspector N17E (Specim), equipped with a 30 μm slit which provides 5 nm spectral resolution, and a linear, PC-controlled movable stage (Middleton Inc.). These components were integrated by Middleton Inc. into a stand-alone image acquisition system. Importantly, this system provided negligible chromatic aberration in the range of 600 to 1600 nm, thus eliminating a known problem in HSI.[13 (link), 14 (link)] To minimize specular reflection from the skin, the lens was appended with a SWIR polarizer (Boulder Optics) embedded in a rotating ring (Thorlabs). Two conventional incandescent 2 × 50 W halogen lamps (type Reveal, GE) with broad output from 400 to 2500 nm were used as the light sources.
The calibration of the system was performed using two laser lines: 1064 nm from the laser diode (Thorlabs) and 1550 nm (PolarOnyx). The laser lines were additionally verified using a spectrophotometer Nanolog equipped with an InGaAs linear diode array detector (Horiba).
+ Open protocol
+ Expand
3

Spectroscopic Characterization of Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
Absorption spectra have been collected by a Varian Cary 500 dual beam spectrophotometer. Steady-state emission are obtained using an FLS 980 (Edinburg Instrument Ltd., Livingston, UK) and a Nanolog (Horiba Scientific, Piscataway, NJ, USA) spectrofluorimeter. The excitation wavelength for the emission spectra was 390 nm.
+ Open protocol
+ Expand
4

Fluorescent Probes for Cancer Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols

N-Hydroxysuccinimidyl ester derivatives of organic dyes, Alexa488–NHS ester and ICG–NHS ester were purchased from Thermo Fisher Scientific and Goryo Chemicals (Japan), respectively. Heceptin, Cyramza, and Kadcyla were purchased from Chugai Pharmaceutical Co., Ltd (Tokyo, Japan). Erbitux was purchased from Merk Serono. Anti-human PD-L1 antibody was purchased from Bio Cell. Normal human IgG was purchased from FUJIFILM Wako Pure Chemical Corp. (Japan). Glutathione-coated PbS QDs (Em: 1250 nm) were prepared by the literature method.36 (link) Intralipid emulsion (20%) was purchased from Sigma-Aldrich. Breast tumour cells (KPL-4) were kindly provided by Dr Kurebayashi (Kawasaki Medical School). Skin tumour cells (A431) were purchased from RIKEN cell bank. Nude mice (five-week-old female BALB/c nu/nu mice) were purchased from SLC Inc (Japan).
Absorption spectra were recorded with a spectrophotometer (Jasco, V-670). Fluorescence spectra were recorded with a spectrofluorometer (NanoLog, HORIBA, Japan). Fluorescence imaging of cancer cells were performed with a fluorescence microscope (BZ-X700, Keyence, Japan). In vivo NIR fluorescence imaging was performed with a fluorescence system (Bruker MS-FX PRO). In vivo SWIR fluorescence imaging was performed with a home-built wide-field microscope system.4a
+ Open protocol
+ Expand
5

Photoluminescence Characterization of Organosilica-C-dots Nanocomposites

Check if the same lab product or an alternative is used in the 5 most similar protocols
PL spectra of organosilica – C-dots nanocomposite films have been recorded with a “NanoLog” Horiba Jobin Yvon spectrofluorometer, Japan: Excitation-fixed spectra at 365 nm and Excitation-Emission-Intensity PL spectra have been recorded with a 450 W xenon lamp as the excitation source. PL spectra have been collected with an excitation range of 250–600 nm and an emission range of 300–650 nm. PL map spectra of C-dots dispersed in different solvents have been recorded using a quartz cuvette with the NanoLog under the same conditions as films.
+ Open protocol
+ Expand
6

Time-Correlated Single Photon Counting of QDs

Check if the same lab product or an alternative is used in the 5 most similar protocols
Time-correlated single photon counting experiments were performed using Horiba, NanoLog series of spectra-fluorometers equipped with Fluoro3PS-Photomultiplier Power Source. NanoLED laser diode with excitation wavelength of 390 nm at repetition rates of 1 MHz was used to excite QDs. The lifetime trajectories of QDs were recorded for 400 ns time durations.
+ Open protocol
+ Expand
7

Optical Characterization of SWCNTs

Check if the same lab product or an alternative is used in the 5 most similar protocols
The optical absorption spectra of the SWCNTs were measured from 250 to 1,350 nm using a UV-vis-NIR spectrometer (UV-3600, Shimadzu) with a quartz cuvette and a path length of 10 mm. The spectral slit width was 2 nm. The photoluminescence spectra of the SWCNTs were measured as a function of excitation and emission wavelengths using a spectrofluorometer (NanoLog, HORIBA) equipped with a liquid nitrogen-cooled InGaAs near-IR array detector. The excitation wavelength was varied from 450 to 850 nm in 5-nm steps, and the emission wavelength was varied from 850 to 1,350 nm. The spectral slit widths were 7 nm for both excitation and emission. The raw data were corrected using instrumental factors. The optical extinction spectrum of mouse skin was measured from 250 to 1,350 nm using a UV-VIS-NIR spectrometer (UV-3700, Shimadzu) equipped with an integrating sphere. The mouse skin was completely removed from the back of a nude mouse and immediately used for the optical measurements. The thickness of the mouse skin was measured using digital calipers and estimated to be 0.35 mm. The spectral slit width was 8 nm.
+ Open protocol
+ Expand
8

Fluorescence Spectroscopy Kinetics Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Fluorescence spectra and continuous kinetics release were recorded using a “NanoLog” Horiba Jobin Yvon spectrofluorometers: 3D and 2D mapping were recorded with a 450 W xenon lamp as the excitation source. 2D maps were collected by using an excitation wavelength at 305 nm and acquiring the emission in the range of 300−700 nm for DA and exciting at 390 nm and acquiring the emission in the range of 400−700 nm for DQ.
+ Open protocol
+ Expand
9

Optical Spectroscopic Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Absorption and PL Spectroscopy:
The absorption spectra were measured with a spectrophotometer (Hitachi, U-4100). The photoluminescence spectra were measured with a fluorophotometer (Horiba Jobin Yvon, NanoLog). The samples were excited at 500 nm and 700 nm for selective excitation of donor and acceptor, respectively.
+ 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!