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![Alexa Fluor 647 NHS esters (or succinimidyl esters) readily react with the primary amines (R-NH<sub>2</sub>) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.](/_next/image?url=https%3A%2F%2Fimages.aatbio.com%2Fproducts%2Ffigures-and-data%2Faf647-nhs-ester-alexa-fluor-647-nhs-ester%2Ffigure-for-af647-nhs-ester-alexa-fluor-647-nhs-ester_Q1zeG.jpg&w=640&q=75)
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![Alexa Fluor 647 NHS esters (or succinimidyl esters) readily react with the primary amines (R-NH<sub>2</sub>) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.](/_next/image?url=https%3A%2F%2Fimages.aatbio.com%2Fproducts%2Ffigures-and-data%2Faf647-nhs-ester-alexa-fluor-647-nhs-ester%2Ffigure-for-af647-nhs-ester-alexa-fluor-647-nhs-ester_Q1zeG.jpg&w=2048&q=100)
Figure 1. Alexa Fluor 647 NHS esters (or succinimidyl esters) readily react with the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.
![Alexa Fluor 647 NHS esters (or succinimidyl esters) readily react with the primary amines (R-NH<sub>2</sub>) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.](/_next/image?url=https%3A%2F%2Fimages.aatbio.com%2Fproducts%2Ffigures-and-data%2Faf647-nhs-ester-alexa-fluor-647-nhs-ester%2Ffigure-for-af647-nhs-ester-alexa-fluor-647-nhs-ester_Q1zeG.jpg&w=640&q=75)
![Alexa Fluor 647 NHS esters (or succinimidyl esters) readily react with the primary amines (R-NH<sub>2</sub>) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.](/_next/image?url=https%3A%2F%2Fimages.aatbio.com%2Fproducts%2Ffigures-and-data%2Faf647-nhs-ester-alexa-fluor-647-nhs-ester%2Ffigure-for-af647-nhs-ester-alexa-fluor-647-nhs-ester_Q1zeG.jpg&w=128&q=25)
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