Nucleic Acid Purity Assessment using A260/A280 Ratios

ثبت نشده
چکیده

A common practice in molecular biology is to perform a quick assessment of the purity of nucleic acid samples by determining the ratio of spectrophotometric absorbance of the sample at 260 nm to that of 280 nm. Here we describe the basis of A260/A280 ratio determinations of nucleic acids and demonstrate the utility of the BioTek PowerWaveTM 200 scanning microplate spectrophotometer to perform this procedure on large numbers of samples.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Nucleic Acid Purity Assessment using A260/A280 Ratios

A common practice in molecular biology is to perform a quick assessment of the purity of nucleic acid samples by determining the ratio of spectrophotometric absorbance of the sample at 260 nm to that of 280 nm. Here we describe the basis of A260/A280 ratio determinations of nucleic acids and demonstrate the utility of the BioTek PowerWaveTM 200 scanning microplate spectrophotometer to perform t...

متن کامل

The Importance of the 240 nm Absorbance Measurement

The assessment of nucleic acid purity by the A260/A280 ratio has been used for a number of years. This measurement, however, does not provide all the information that investigator needs to assess nucleic acid preparations. The detection of impurities common to nucleic acid preparations that are not detected with absorbance measurements at 260 nm and 280 nm can in most instances be accomplished ...

متن کامل

Micro-Volume Purity Assessment of Nucleic Acids using A260/A280 Ratio and Spectral Scanning

The spectrophotometric analysis of biomolecules for sample quantification and purity assessment has been well documented. Quantification is made possible by the absorption of ultra-violet light by chromophores contained in nucleic acids and protein. Consistent with these methods is the use of the Beer-Lambert Law that relates physical property of light absorption by molecules to concentration w...

متن کامل

Purification of intact nucleic acid from samples

is required for many molecular biology applications. Accurate PCR replication of RNA and DNA sequences requires complete removal of cellular lipids and proteins. Likewise, most restriction endonucleases used to digest genomic DNA are inactivated or degraded by cellular proteases normally present prior to purification of the nucleic acids. Thus, failure to remove these cellular contaminants ofte...

متن کامل

Measurement of 8-OHdG in DNA by HPLC/ECD: the importance of DNA purity.

DNA has been considered to be pure when the ratio of absorbance at 260 nm over the absorbance at 280 nm (A260/A280) is 1.8 (8). This definition of purity, however, is based more upon a functional assessment (e.g., ability to cut the DNA with restriction enzymes) than upon more conventional analytical criteria. In a recent article, Glasel reexamined the significance of the A260/A280 (3). He note...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2006