Related Experiment Video

Updated: May 22, 2026

High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels
10:07

High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels

Published on: January 27, 2013

A novel di-triazole based peptide as a highly sensitive and selective fluorescent chemosensor for Zn2+ ions

Sambasivarao Kotha1, Deepti Goyal née Bansal, Subhasree Banerjee

  • 1Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400 076, India. srk@chem.iitb.ac.in

The Analyst
|May 12, 2012
PubMed

More Related Videos

Characterizing Mammalian Zinc Transporters Using an In Vitro Zinc Transport Assay07:55

Characterizing Mammalian Zinc Transporters Using an In Vitro Zinc Transport Assay

Published on: June 2, 2023

Quantifiable and Inexpensive Cell-Free Fluorescent Method to Confirm the Ability of Novel Compounds to Chelate Iron05:36

Quantifiable and Inexpensive Cell-Free Fluorescent Method to Confirm the Ability of Novel Compounds to Chelate Iron

Published on: February 23, 2024

Related Concept Videos

Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.