AcuGenix™ RNA Fast Plant Extraction Kit
11-Minute High-Purity RNA Isolation for Challenging Plant Tissues – No Phenol, No DNase, No Compromise

Product overview
The AcuGenix™ RNA Fast Plant Extraction Kit is engineered for the rapid isolation of high-quality total RNA from 50-150 mg of diverse plant tissues, including samples from common species as well as polyphenol- and polysaccharide-rich tissues (roots, stems, leaves, flowers, fruits, seeds, etc.). It is optimized for plant molecular biology workflows requiring reliable, inhibitor-free RNA input.
Features and applications
- Broad Compatibility with Challenging Tissues: Validated for both standard and recalcitrant plant samples with high levels of secondary metabolites (polyphenols, polysaccharides) that typically compromise RNA quality.
- Safe, Toxic-Reagent-Free Workflow: Eliminates the need for hazardous phenol-chloroform extraction, β-mercaptoethanol, DTT, and DNase I digestion, reducing operator exposure risk and waste disposal burden.
- Ultra-Rapid 11-Minute Protocol: The entire extraction workflow is completed in just 11 minutes following sample homogenization, drastically reducing hands-on time compared to conventional column- or phenol-based methods.
- Efficient gDNA and Impurity Removal: The included gDNA-Filter Column removes genomic DNA and cellular impurities, while the Pure RNA Column I ensures high-efficiency RNA binding for consistent yield.
- Exceptional RNA Purity & Integrity: Rapid lysis suppresses nucleases released during cell disruption to preserve RNA integrity. Isolated RNA is free of protein, genomic DNA, and other contaminants that interfere with downstream assays.
- Culture Cell Compatibility: Also validated for high-purity RNA extraction from plant cell cultures, supporting diverse experimental models.
- Seamless Downstream Compatibility: Purified RNA requires no additional cleanup and is directly compatible with the full AcuGenix™ line of reverse transcription and NGS library preparation kits.
- Gene expression analysis via RT-PCR and quantitative real-time RT-PCR (qRT-PCR)
- Transcriptome profiling and RNA-seq library construction
- Plant pathogen detection and viroid RNA isolation
- Northern blotting and RNA structure analysis
- In vitro translation and protein expression studies
- Molecular cloning and gene functional analysis
- Microarray-based gene expression profiling
- Non-model plant genomics and molecular breeding research
Components
| Components | Specification/Notes |
|---|---|
| PLB Reagent | 30 mL |
| Buffer RWA 1 | 9.6 mL |
| Buffer RWB 1 | 12 mL |
| Proteinase K | 0.5 mL |
| RNase-free ddH2O | 10 mL |
| gDNA-Filter Columns (each in a 2 mL Collection Tube) | 50 T |
| Pure RNA Columns I (each in a 2 mL Collection Tube) | 50 T |
| RNase-free Collection Tubes 1.5 mL | 50 T |
Performance data
Broad Sample Compatibility


High-quality extracted RNA


Note: The absence of genomic DNA contamination eliminates the need for post-extraction DNase treatment, avoiding RNA degradation risks; high-integrity RNA ensures accurate quantification and reliable data for qPCR and RNA-seq workflows.
Extract Performance/Target Amplification Performance

Note: Lower Ct values indicate higher RNA integrity and purity, with fewer PCR inhibitors and better template availability; these results confirm BR2B202 supports robust gene expression analysis and variant detection workflows in plant research.
Shipping and storage
| Condition | Recommendation |
|---|---|
| Storage | Store at room temperature (15–25°C). |
| Shipping | Refer to product label and shipping documentation. |
Downloads
Need this product lyophilized, in bulk, or in a custom format?
The feasibility assessment is free of charge. Send the assay brief and target format.




