The largest database of trusted experimental protocols

Agilent uv visible spectrophotometer

Manufactured by Agilent Technologies
Sourced in United States

The Agilent UV–visible spectrophotometer is a laboratory instrument that measures the absorption or transmittance of light in the ultraviolet and visible regions of the electromagnetic spectrum. It is designed to quantify the concentration of chemical species in a sample.

Automatically generated - may contain errors

2 protocols using agilent uv visible spectrophotometer

1

Total Polyphenol Content Determination

Check if the same lab product or an alternative is used in the 5 most similar protocols
The samples’ total polyphenol (TP) content was determined using the Folin Ciocalteu colorimetric method as described by Blainski et al. [54 (link)] with slight modification. Briefly, 200 µL of the sample aqueous extract was mixed with 300 µL 2% Na2CO3 (Fisher Scientific, Waltham, MA, USA), 50 µL Folin-Ciocalten’s reagent (Sigma-Aldrich Co., St. Louis, MO, USA), and 1 mL of distilled water and left for 1 h at room temperature in total darkness. Gallic acid (Sigma-Aldrich, St. Louis, MO, USA) was used as a standard. The absorbance was measured by Agilent UV–visible spectrophotometer (Agilent 8453, Palo Alto, CA, USA) at 765 nm, and the results were expressed as mg Gallic acid equivalents (mg GAE/100 g of the sample).
+ Open protocol
+ Expand
2

Cytotoxicity Evaluation of Novel Compound

Check if the same lab product or an alternative is used in the 5 most similar protocols
The required chemicals were purchased from Sigma-Aldrich (Seoul, South Korea) and used as received. The A549 cells for the cytotoxicity study were purchased from the Korea cell line bank, Seoul, South Korea. 3-(4, 5-dimethyl thiazol-2yl)-2, 5-diphenyl tetrazolium bromide (MTB), fetal bovine serum (FBS), trypsin, and dulbecco Modified Eagle Medium (DMEM) were procured from Thermo Fisher Scientific, Waltham, MA, USA. The glass coverslips, cell culture plates, 96 well plates required for cell cytotoxicity assay were obtained from SPL Life Sciences, Seoul, Korea. The FT-IR spectra was recorded in the 4000–400 cm−1 region with a Shimadzu FTIR spectrophotometer (Shimadzu, Kyoto, Japan) using KBr pellet. The 1H NMR and 13C NMR spectra were recorded on a Bruker AVANCE-500 (400 MHz) spectrometer (Bruker, Billerica, UK) using DMSO-d6 as a solvent. The UV-Visible spectra were recorded on an Agilent UV-Visible spectrophotometer (Agilent Technologies, Santa Clara, CA, USA). Single-crystal X-ray diffraction experiments were performed using an Xcalibur, Sapphire3, Gemini ultra diffractometer equipped with an Oxford Cryosystems 700 Series (Agilent Technologies, Santa Clara, CA, USA) low-temperature apparatus operating at T = 120(2) K. Spectramax Plus 384 (Molecular Devices, San Jose, CA, USA) microplate reader was used for this study.
+ 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!