Sodium Azide Immobilization

Sodium azide immobilization is a biological technique that temporarily arrests cellular or microbial activity using sodium azide, a potent metabolic inhibitor. Sodium azide disrupts cytochrome c oxidase in the electron transport chain, suppressing oxidative phosphorylation, ATP production, and energy-dependent movement or growth. In biological laboratories, this principle helps preserve certain antibody and protein preparations, limit microbial proliferation, and reduce metabolic activity during sample handling or storage. Because sodium azide is highly toxic and can form hazardous compounds with some metals and acids, its use requires controlled conditions, appropriate protective measures, and specialized waste management.

Sodium Azide Immobilization - Related Videos

Research

JoVE Journal - Bioengineering

Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization

0 Views •

Cited by 23 •

2012

This article will describe the procedure for synthesizing a hydrophobically modified Nafion enzyme immobilization membrane and how to immobilize proteins and/or enzymes within the membrane and test their specific activity.

An Optimized Protocol for the Efficient Radiolabeling of Gold Nanoparticles by Using a 125I-labeled Azide Prosthetic Group

0 Views •

Cited by 5 •

2016

A detailed procedure for the synthesis of a 125I-labeled azide and the radiolabeling of dibenzocyclooctyne (DBCO)-group-conjugated, 13-nm-sized gold nanoparticles using a copper-free click reaction is described.

Wet Chemistry and Peptide Immobilization on Polytetrafluoroethylene for Improved Cell-adhesion

0 Views •

Cited by 9 •

2016

Cell-adhesiveness is key to many approaches in biomaterial research and tissue engineering. A step-by-step technique is presented using wet-chemistry for the surface modification of the important polymer PTFE with peptides.

Education

JoVE Core - Organic Chemistry

Preparation of 1° Amines: Azide Synthesis

0 Views •

2023

Direct alkylation of ammonia produces polyalkylated amines, along with a quaternary ammonium salt. To exclusively prepare primary amines, the azide synthesis method can be used. Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units

0 Views •

Cited by 1 •

2016

Here, we present a protocol to synthesize a complex organic compound comprised of three nonplanar polyaromatic units, assembled easily with reasonable yields.

View All Results

FAQs

Related Topics