Isolation of an adequate quantity of high-quality RNA is a crucial step in gene expression analysis. Difficulties in sampling and RNA extraction of field-grown crops, especially from roots, are substantial obstacles to understanding actual gene expression in the field. We examined the effectiveness of the RNA extraction method (FRP) using pot- and field-grown soybean roots. High quantity and quality of total RNA could extract by the FRP method from both pot- and field-grown soybean roots at different growth stages. To determine the influence of root washing during the sampling process, roots were washed with water for 5 s, 1 min, and 5 min, then analyzed for aquaporin gene expression levels. Root washing for 5 min affected gene expression o...
Nucleic acids extraction from mangroves as woody plants needs lots of practical experience. In the p...
Quantitative reverse transcription polymerase chain reaction (qRT-PCR) is widely used to analyze the...
Abstract – The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), g...
Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differential gene e...
Plant microRNAs are small non-coding, endogenic RNA molecule (containing 20-24 nucleotides) produced...
<div><p>Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differentia...
The isolation of high quality RNA is a crucial technique in plant molecular biology. The quality of ...
A number of cDNA clones to independent mRNAs that increase in amount after brief exposure to auxins ...
The RNAzol RT reagent was used to provide pure RNA from human cells. We develop a protocol using RNA...
Studies of plant gene expression today need pure preparations of high-yielding undegraded RNA. This ...
An RNA extraction method with high integrity and purity as well as the selection of adequate referen...
The availability of the soybean genome sequence and the rapid evolution of DNA sequencing technologi...
ABSTRACT The Straw Test is an assay developed to evaluate the resistance of common bean to white mol...
Background: Soybean (Glycine max) production is significantly hampered by frequent droughts in many ...
Small RNAs are non-protein coding RNAs that regulate gene expression in plants primarily by cleaving...
Nucleic acids extraction from mangroves as woody plants needs lots of practical experience. In the p...
Quantitative reverse transcription polymerase chain reaction (qRT-PCR) is widely used to analyze the...
Abstract – The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), g...
Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differential gene e...
Plant microRNAs are small non-coding, endogenic RNA molecule (containing 20-24 nucleotides) produced...
<div><p>Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differentia...
The isolation of high quality RNA is a crucial technique in plant molecular biology. The quality of ...
A number of cDNA clones to independent mRNAs that increase in amount after brief exposure to auxins ...
The RNAzol RT reagent was used to provide pure RNA from human cells. We develop a protocol using RNA...
Studies of plant gene expression today need pure preparations of high-yielding undegraded RNA. This ...
An RNA extraction method with high integrity and purity as well as the selection of adequate referen...
The availability of the soybean genome sequence and the rapid evolution of DNA sequencing technologi...
ABSTRACT The Straw Test is an assay developed to evaluate the resistance of common bean to white mol...
Background: Soybean (Glycine max) production is significantly hampered by frequent droughts in many ...
Small RNAs are non-protein coding RNAs that regulate gene expression in plants primarily by cleaving...
Nucleic acids extraction from mangroves as woody plants needs lots of practical experience. In the p...
Quantitative reverse transcription polymerase chain reaction (qRT-PCR) is widely used to analyze the...
Abstract – The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), g...