A method is described for measuring the deoxyribonucleic acid (DNA) content of small samples of adipose tissue or free fat cells. Lipids and acid-soluble nucleotides are first removed by extraction with a cold diethyl ether - ethanol mixture containing 10 per cent. ml V of trichloroacetic acid. DNA is then measured by hydrolysing the nucleoprotein residue in a 5 per cent. solution of trichloroacetic acid at 90 QC for 20 min, followed by treatment with p-nitrophenylhydrazine and measurement of the hydrazone at 560 nm. Several aspects of the method have been critically examined in order to determine the optimum conditions. The method is satisfactorily reproducible
Background and aims: Adipose tissue (AT) fatty acid (FA) composition is considered to be the gold st...
Sensitive and safe methods for visualization of DNA in agarose gels are described. 0.001% crystal vi...
A simple method allowing quantitative purification of the ribonucleotides obtained by alcaline hydro...
A sensitive and simple method for the quantitation of human DNA is described. This method Is based o...
Alkaline solutions (0.1–0.5N NaOH) at elevated temperatures can be used to extract DNA from small pi...
Full text of this article is not available in SOAR.The separation of common and modified deoxyribonu...
A sensitive (5 to 100g) and reproducible (±3.54 % SD) method is described for determining monoglycer...
A simple, rapid method for isolating human DNA has been developed, which can be routinely used in cl...
One of the most sensitive and specific methods for quantitative estimation of deoxyribonucleic acid ...
Genetic markers of diseases can be studied post-mortem with the isolation of DNA from tissues. Whil...
Techniques for derivatisation of fatty acids to form compounds suitable for detection by High Perfor...
Using nuclei isolated from less than 0.2 g tissue or 107 cells, a method is presented for the quanti...
Alterations in global DNA methylation are implicated in various pathophysiological processes. The de...
We present a new technique for evaluating epidermal DNA synthesis as measured by incorporation of tr...
A method for the estimation of DNA and RNA in rat brain is described. The principal modifications of...
Background and aims: Adipose tissue (AT) fatty acid (FA) composition is considered to be the gold st...
Sensitive and safe methods for visualization of DNA in agarose gels are described. 0.001% crystal vi...
A simple method allowing quantitative purification of the ribonucleotides obtained by alcaline hydro...
A sensitive and simple method for the quantitation of human DNA is described. This method Is based o...
Alkaline solutions (0.1–0.5N NaOH) at elevated temperatures can be used to extract DNA from small pi...
Full text of this article is not available in SOAR.The separation of common and modified deoxyribonu...
A sensitive (5 to 100g) and reproducible (±3.54 % SD) method is described for determining monoglycer...
A simple, rapid method for isolating human DNA has been developed, which can be routinely used in cl...
One of the most sensitive and specific methods for quantitative estimation of deoxyribonucleic acid ...
Genetic markers of diseases can be studied post-mortem with the isolation of DNA from tissues. Whil...
Techniques for derivatisation of fatty acids to form compounds suitable for detection by High Perfor...
Using nuclei isolated from less than 0.2 g tissue or 107 cells, a method is presented for the quanti...
Alterations in global DNA methylation are implicated in various pathophysiological processes. The de...
We present a new technique for evaluating epidermal DNA synthesis as measured by incorporation of tr...
A method for the estimation of DNA and RNA in rat brain is described. The principal modifications of...
Background and aims: Adipose tissue (AT) fatty acid (FA) composition is considered to be the gold st...
Sensitive and safe methods for visualization of DNA in agarose gels are described. 0.001% crystal vi...
A simple method allowing quantitative purification of the ribonucleotides obtained by alcaline hydro...