Antifungal drugs

Synonyms: 5-Fluoro-1H-indole-2,3-dione 5-Fluoroindoline-2,3-dione Purity Limit: &ge 98% CAS No.: 443-69-6 Molecular Formula: C8H4FNO2 Molecular Weight: 165.12 MDL No.: MFCD00022795 Storage Temperature: Store at 0-8°C

Synonyms: 5-Fluoro-1H-indole-2,3-dione 5-Fluoroindoline-2,3-dione Purity Limit: &ge 98% CAS No.: 443-69-6 Molecular Formula: C8H4FNO2 Molecular Weight: 165.12 MDL No.: MFCD00022795 Storage Temperature: Store at 0-8°C

Application 5-Fluoroorotic acid hydrate has also been used as a counter-selection agent to screen L. lactis (multi) peptidase knockout mutants and C.

Application 5-Fluoroorotic acid hydrate has also been used as a counter-selection agent to screen L. lactis (multi) peptidase knockout mutants and C.

Application 5-Fluoroorotic acid hydrate has also been used as a counter-selection agent to screen L. lactis (multi) peptidase knockout mutants and C.

Useful in the selection of orotidine-5′-phosphate decarboxylase mutants of Saccharomyces cerevisiae.

Using 5-Fluoroorotic Acid (5-FOA) for the counter-selection of yeast is a common genetic screening method. Curing yeast strains of plasmids, plasmid shuffling, allelic replacement, and two-hybrid screens are methods that can employ the use of 5-FOA.

Using 5-Fluoroorotic Acid (5-FOA) for the counter-selection of yeast is a common genetic screening method. Curing yeast strains of plasmids, plasmid shuffling, allelic replacement, and two-hybrid screens are methods that can employ the use of 5-FOA.

5-FLUOROSULFONYL-2-(HEXADECYLSULFONYL)-BENZOIC ACID-

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

5-Hydroxy-2-methyl-4-chromanone is an antitumor compound. Weakly antibacterial and antifungal. Mediates a unique cross-linking reaction between DNA and histone H3 by photoactivation.

5-Hydroxy-2-methyl-4-chromanone is an antitumor compound. Weakly antibacterial and antifungal. Mediates a unique cross-linking reaction between DNA and histone H3 by photoactivation.