• 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 The kit uses nanomagnetic beads with unique separation effects and a special buffer system to extract high-quality genomic DNA from plant tissue samples. The entire extraction process is safe and convenient, and the extracted genomic DNA has a high yield, high purity, and stable and reliable quality. The magnetic bead separation system of the kit is particularly suitable for use with high-throughput automated workstations.
Item No./Specification/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.
Application
For plant RNA extraction
Product composition
Product Performance
  • Universal type, compatible with various sample types, high DNA extraction yield and good purity.
Fig.1A The amount of DNA extracted from 150 mg fresh tissues of different species using the Qihengxing Plant Extraction Kit


Fig1.B Analysis of the purity of extracted DNA (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 green radish.
  • 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 dry samples of pine needles were extracted using the Qihengxing plant extraction kit and the supplier T plant extraction kit, respectively. The input amount of fresh samples was 150 mg and the input amount of dry samples was 30 mg. The extracted DNA was subjected to quantitative and purity analysis.
  • The extracted DNA contains few residual inhibitors, and the qPCR results are accurate and free of inhibition.
The GAPDH gene of human gDNA was used as IPC (Internal Positive Control) for quantitative analysis: 10 μL reaction system, 1 ng human gDNA, 10% (v/v) DNA extraction products of green radish, corn, pine needles and water were added respectively, and qPCR analysis was performed. The addition of DNA extraction products of green radish, corn, and pine needles had no effect on the amplification linearity and no inhibition on PCR.

Fig.3 There are few inhibitors in DNA extract and no inhibitory effect on qPCR.
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