The Hieff^TM Plant RNA Kit is suitable for extracting RNA from polysaccharide polyphenol plants such as Arabidopsis thaliana, rice, maize, wheat, tomato, tobacco, cotton and Holly. The extraction and purification of total RNA from plant samples (100-200 mg fresh or cryopreserved samples) can be completed within 40 minutes without the use of toxic organic substances such as phenol and chloroform. The silicon matrix material used in the centrifugal adsorption column is a unique new material of our company, which can maximize the recovery of high-purity RNA with our unique lysis solution formula. DNase I directly digests gDNA on the column, and the extracted total RNA has high purity, stable and reliable quality, and can be applied to various downstream application experiments, such as RT-PCR, RT-qPCR, in vitro transcription, molecular cloning etc.

Features

Safety: no need to use organic reagents such as phenol chloroform.

Fast: RNA extraction from samples can be completed within 40 min minutes.

Widely compatibility: It is suitable for RNA extraction from Arabidopsis thaliana, rice, corn, wheat, tomato, tobacco, cotton, holly and other simple polysaccharide and polyphenol plant samples.

Low genome residue: equipped with DNase I, which can effectively remove DNA pollution.

Applications

Plant RNA extraction;Total RNA extraction from plants;

Specifications

Components

Shipping and Storage

Part I should be stored at -25~-15℃ for 2 years.

Part II should be stored at room temperature for 2 years.

Figures

RNA was extracted from Rice, corn, Arabidopsis, tomato. The extracted RNA was then subjected to agarose gel electrophoresis, and the electrophoretogram is shown below.

Table 1. High quality of extracted products. 

FAQ

Q: Can the plant RNA extraction kit also be used for extracting RNA from fungi?

A: You can give it a try.

Q: What are the samples of polysaccharides and polyphenols?

A: Cotton, coniferous trees, ginkgo; the flesh of bananas and grapes; the seeds of wheat and peanuts; fungi such as mushrooms, etc.

Q: Why are two columns used for extraction?

A: DNA filtration column: Specifically adsorbs DNA from the tissue lysate and filters out the solid substances in the lysate. RNA adsorption column: Specifically adsorbs RNA.

Q: RNA Degradation

A: The samples were repeatedly subjected to freezing and thawing, or there was contamination with RNase during the extraction process.

Q: Low RNA production

A: If the starting amount of the sample is too high or the material is not fully lysed, it is recommended to use a smaller amount of sample and thoroughly grind or homogenize it.

Q: There is genomic DNA contamination.

A: The initial sample input volume was too high. The initial input volume should be reduced. Alternatively, in subsequent experiments, a reverse transcription kit with the removed genomic material can be selected for removal.

Documents:

Safety Data Sheet

19291_MSDS_HB20250409_EN.PDF

Manuals

19291_Manual_Ver.EN20250825.pdf

Citations & References: