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391 Technology Way, Suite 168 Winston-Salem, NC 27101 Telephone: 6173363228 Fax: 8667279826 Web: www.kerafast.com Email: info kerafast.com Material Safety Data Sheet This Acetate EDTA, TAE Section
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First, prepare a working solution of tris acetate edta tae by adding the appropriate amount of tris-EDTA buffer to distilled water. The final concentration of tris acetate and EDTA should be determined based on the specific experiment or application.
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Mix the solution thoroughly to ensure that the tris acetate and EDTA are dissolved completely.
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Researchers and scientists working in molecular biology, genetics, and related fields often require tris acetate edta tae for various applications. It is commonly used in processes like agarose gel electrophoresis, DNA and RNA isolation, and DNA fragment analysis.
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Tris acetate EDTA (TAE) is a buffer solution commonly used in molecular biology techniques such as agarose gel electrophoresis.
Scientists, researchers, and lab technicians who conduct experiments involving DNA and RNA analysis may be required to prepare and use tris acetate EDTA (TAE) buffer.
Tris acetate EDTA (TAE) buffer can be prepared by mixing the appropriate amounts of Tris base, acetic acid, and EDTA in water to reach the desired pH level.
The purpose of tris acetate EDTA (TAE) buffer is to provide a stable pH environment for DNA and RNA molecules during electrophoresis, allowing them to migrate through the gel effectively.
The composition of tris acetate EDTA (TAE) buffer and the pH level must be documented when using it in experiments.
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