• StarPure Universal Plant DNA Extraction Kit
  • StarPure Universal Plant DNA Extraction Kit

StarPure Universal Plant DNA Extraction Kit

No.FS-B1303/FS-B1303-S
StarPure Universal Plant DNA Extraction Kit This kit utilizes unique nanomagnetic beads and a specialized buffer system to extract high-quality genomic DNA from plant tissue samples. The entire extraction process is safe and convenient, resulting in high yield, high purity, and consistent, reliable genomic DNA. The magnetic bead separation system in this kit is particularly well-suited for use with high-throughput automated workstations.
Item No./Specifications/Price:
FS-B1303/100 rxns/¥2700.00
FS-B1303-S/30 rxns/¥1000.00
  • StarPure Universal Plant DNA Extraction Kit

Product Description

StarPure Universal Plant DNA Extraction Kit
StarPure Universal Plant DNA Extraction Kit



Product Advantages
  • The kit is based on nanomagnetic bead nucleic acid purification technology and is suitable for manual extraction and automated workstation extraction;
  • The extracted products can be directly used for PCR, nucleic acid hybridization, second-generation sequencing, etc.
  • This product does not require organic reagents such as phenol/chloroform, and the operation process is safe and fast.
Product Application
For plant RNA extraction
Product components
Product Performance
  • Universal, compatible with various sample types, with high DNA extraction yield and good purity.
Fig.1A DNA amount extracted from 150 mg fresh tissues of different species using the Qihengxing Plant Extraction Kit


Fig1.B Analysis of extracted DNA purity (260/280 value)



Fig.1C Electrophoresis results of the extracted DNA. Numbers 1-15 are: cotton leaves, corn leaves, rice, wheat, dandelion leaves, plantain, hawthorn leaves, ginkgo leaves, rose petals, pine needles, violet, pepper, cypress, green onion, and pothos.
  • For difficult sample tissues, such as oily pine needle samples, the Qihengxing plant extraction kit performs better than other suppliers in terms of DNA yield.




Fig.2 Fresh and dried pine needle samples were extracted using the Qihengxing plant extraction kit and the supplier T plant extraction kit, respectively. The input amount of fresh sample was 150 mg and the input amount of dry sample was 30 mg. The extracted DNA was quantitatively analyzed and its purity was analyzed.
  • The extracted DNA contains few residual inhibitors, and the qPCR results are accurate and inhibition-free.
Quantitative analysis was performed using the GAPDH gene from human gDNA as an IPC (Internal Positive Control): 10 μL reaction system, 1 ng of human gDNA, 10% (v/v) DNA extracts from scintillation, corn, and pine needles, and water were added for qPCR analysis. The addition of DNA extracts from scintillation, corn, and pine needles had no effect on amplification linearity and did not inhibit PCR.

Fig.3 DNA extracts contain few inhibitors and have no inhibitory effect on qPCR.
Related Product Links

Nucleic acid extraction and purification products

Download

We use Cookie To improve your online experience. By continuing to browse this site, you agree to our use of Cookie .