In this article, we describe a new procedure to map 5\u2032 ends of RNAs. The procedure consists in the use of specific RNase H digestion of a hybrid formed by the RNA and a complementary DNA oligonucleotide. Northern blot hybridization of the resulting RNA fragment allows an accurate measurement of its length. Although we generally use this procedure as a control of previously performed primer extension analyses, the absence of nonspecific bands, which often occur in primer extensions on RNA templates with extended secondary structures, suggests that our method may be preferable when these difficult templates are analyzed
Class IIS restriction enzymes, a subgroup of class II, cleave DNA at a precise location outside thei...
Abstract Background As a powerful tool, RNA-Seq has been widely used in various studies. Usually, un...
Structure mapping is a classic experimental approach for determining nucleic acid structure that has...
In this article, we describe a new procedure to map 5′ ends of RNAs. The procedure consists in the u...
An important problem often faced in the molecular characterization of genes is the precise mapping o...
<p>(A) Schematic representation of the two methods applied to map regions which are accessible to ol...
<p>The 5′-bases of mono-phosphorylated RNA (asterisks) were identified using the following technique...
We describe a simple method for 3′-end labeling RNAs of known sequence. A short DNA template is desi...
<p>Semi-random libraries of DNA 6-mers and RNase H hydrolysis of RNA-DNA hybrids were used to search...
Abstract A method is described that allows an accurate mapping of 3' ends of RNAs. In this method a ...
A method is described for the direct sequence analysis^of 20-25 nucleotides from the termini of 5&ap...
Primer extension is one of the most common methods used to measure the amount and size of RNAs. We d...
The 5′ untranslated regions of mRNA play an important role in their translation.Here, we describe th...
The preparation of small RNA cDNA sequencing libraries depends on the unbiased ligation of adapters ...
A convenient nucleotide sequencing method for 5'end protein-linked RNAs was developed. Genome o...
Class IIS restriction enzymes, a subgroup of class II, cleave DNA at a precise location outside thei...
Abstract Background As a powerful tool, RNA-Seq has been widely used in various studies. Usually, un...
Structure mapping is a classic experimental approach for determining nucleic acid structure that has...
In this article, we describe a new procedure to map 5′ ends of RNAs. The procedure consists in the u...
An important problem often faced in the molecular characterization of genes is the precise mapping o...
<p>(A) Schematic representation of the two methods applied to map regions which are accessible to ol...
<p>The 5′-bases of mono-phosphorylated RNA (asterisks) were identified using the following technique...
We describe a simple method for 3′-end labeling RNAs of known sequence. A short DNA template is desi...
<p>Semi-random libraries of DNA 6-mers and RNase H hydrolysis of RNA-DNA hybrids were used to search...
Abstract A method is described that allows an accurate mapping of 3' ends of RNAs. In this method a ...
A method is described for the direct sequence analysis^of 20-25 nucleotides from the termini of 5&ap...
Primer extension is one of the most common methods used to measure the amount and size of RNAs. We d...
The 5′ untranslated regions of mRNA play an important role in their translation.Here, we describe th...
The preparation of small RNA cDNA sequencing libraries depends on the unbiased ligation of adapters ...
A convenient nucleotide sequencing method for 5'end protein-linked RNAs was developed. Genome o...
Class IIS restriction enzymes, a subgroup of class II, cleave DNA at a precise location outside thei...
Abstract Background As a powerful tool, RNA-Seq has been widely used in various studies. Usually, un...
Structure mapping is a classic experimental approach for determining nucleic acid structure that has...