Place the sample on the detection window of the integrating sphere (slide upward) and cover the illuminated spot. The spectrum of the sample was measured within the NIRS range of 12,000–4000 cm−1 for the selected resolution and for the total number of scans. Select the resolution at 2, 4, 8 and 16 cm-1 in order to obtain sufficient infrared spectrum information from the sample in the shortest time. At each resolution condition, 16, 32, 64, and 128 scans were obtained to reduce noise with each scan. Each CRC tissue sample was randomly selected from 3 locations for measurement. Under the same conditions, the background spectrum was measured first, and then the sample spectrum was measured to eliminate the interference of the background signals with the sample spectrum.
Nicolet is50 ft ir analyzer
The Nicolet iS50 FT-IR analyzer is a Fourier Transform Infrared (FT-IR) spectrometer designed for analytical applications. It provides accurate and reliable infrared spectroscopic analysis of samples. The instrument uses an interferometer to generate and detect infrared light, enabling the measurement of absorption or transmission spectra of various materials.
Lab products found in correlation
2 protocols using nicolet is50 ft ir analyzer
NIRS Tissue Sample Characterization
Place the sample on the detection window of the integrating sphere (slide upward) and cover the illuminated spot. The spectrum of the sample was measured within the NIRS range of 12,000–4000 cm−1 for the selected resolution and for the total number of scans. Select the resolution at 2, 4, 8 and 16 cm-1 in order to obtain sufficient infrared spectrum information from the sample in the shortest time. At each resolution condition, 16, 32, 64, and 128 scans were obtained to reduce noise with each scan. Each CRC tissue sample was randomly selected from 3 locations for measurement. Under the same conditions, the background spectrum was measured first, and then the sample spectrum was measured to eliminate the interference of the background signals with the sample spectrum.
Optimizing NIR Spectroscopy for Sample Analysis
A sample (glass slide up) was placed on the detection window of the integrating sphere and was covered by a lid with a gold inner top. The transflectance spectra for the samples were measured in the range of 12,000–4000 cm−1 while using the selected resolution and the selected number of co-added scans. The resolution was selected from 2, 4, 8, and 16 cm−1 to obtain sufficient sample information in a shorter time; the number of co-added scans was selected from 16, 32, 64, and 128 to reduce the noise in a shorter time. Each sample was measured at three tissue locations. The mutant and wild-type samples were alternatively measured. The background spectrum was measured, prior to the sample spectra, under the same conditions to eliminate any ambient interferences on the sample spectra.
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