EasyPure® Plant RNA Kit provides a simple and fast column based method to isolate RNA from plant tissue. Samples are lysed
with detergent to inactivate RNase. DNA is digested with DNase I. RNA is bound to silica membrane. After washing, high quality
RNA is eluted from the column. RNA is free of protein contamination, and is suitable for RTPCR, qRT-PCR, Microarray analysis
and Northern blot.
Storage
DNase I and DNase I Reaction Buffer at -20°C for one year; others at room temperature (15-25°C) for one year.
Shipping
DNase I and DNase I Reaction Buffer on dry ice (-70 °C); others at room temperature.
Gulati J, Kim SG, Baldwin IT, et al. Glutamate Receptor Like Channel 3.3 is involved in mediating glutathione-triggered cytosolic Ca3+ transients, transcriptional changes and innate immunity responses in Arabidopsis[J]. Plant Physiology, 2013, 162(2):1042-59.
Liu Y , Yang S , Song Y , et al. Gain-of-function analysis of poplar, CLE, genes in Arabidopsis by exogenous application and over-expression assays[J]. Journal of Experimental Botany, 2016, 67(8):2309-24.
Chen S , Yuan N , Schnabel G , et al. Function of the genetic element 'Mona' associated with fungicide resistance in Monilinia fructicola[J]. Molecular Plant Pathology, 2017, 18(1):90-97.
Vijayata S , Artemis P , Kim S Y , et al. Tyrosine-610 in the Receptor Kinase BAK1 Does Not Play a Major Role in Brassinosteroid Signaling or Innate Immunity[J]. Frontiers in Plant Science, 2017, 8:1273.
Tongjin L , Xiaohui Z , Haohui Y , et al. Aromatic Glucosinolate Biosynthesis Pathway in Barbarea vulgaris and its Response to Plutella xylostella Infestation[J]. Frontiers in Plant Science, 2016, 8(7):83.
Bio-Medicine
In Vitro Diagnostics
PCR, RT-PCR, qPCR, qRT-PCR
Restriction/Modifying Enzymes
DNA Molecular Weight Standards
Cloning and Mutagenesis System
Nucleic Acid Purification
Next Generation Sequencing
Gene Expression
Protein Analysis
Protein MW Standards
Cell Culture and Detection
Exosome Related
Serum-free medium
Antibodies
ELISA
Instruments
Residual DNA Detection
