Cat.No.:D02111A
Price: ¥
Specifications:
Plant Tissue Direct Amplification PCR Master Mix (2×) This product is a highly efficient direct amplification reagent specially developed to overcome the PCR inhibition barriers in plant samples. It is designed to address the complex inhibitors such as polysaccharides and polyphenols commonly found in plant tissues. Relying on inhibitor-tolerant DNA polymerase and exclusive enhanced buffer system, this product demonstrates outstanding anti-inhibition performance. During the experiment, simply crushing the tissues like leaves, seeds or root tips is sufficient to directly use them as templates for amplification, eliminating the need for conventional DNA extraction and purification steps. This reagent ensures accurate and stable amplification results while significantly simplifying the sample pre-treatment process, providing a reliable and efficient solution for plant molecular biology research.
Plant inhibitor tolerance: Exhibits outstanding tolerance to plant-specific inhibitors such as polyphenols, polysaccharides, tannins, etc.;
One-step lysis direct amplification: After punching holes or grinding the leaves, they are directly added to the reaction system;
High-throughput compatibility: Compatible with 96/384 well plate automated operations;
High success rate: Verified effective for major crops such as rice, wheat, corn, soybeans, and Arabidopsis thaliana.
| Item No. | Component | Specification | Quantity |
| B02121A | Plant Tissue Direct PCR Master Mix (2×) | 1 mL | 1 |
| B02121A | Plant Tissue Direct PCR Master Mix (2×) | 1 mL | 5 |
Store at -20℃ and transport at ≤0℃
Positive identification of transgenic plants, screening of crop germplasm resources, detection of plant pathogens (fungi, bacteria, viruses), genotyping of plant leaves/seeds, identification of callus tissues, etc.
Can this kit be used for amplification of frozen-stored leaves?
Sure, both frozen (-20 degrees Celsius and -80 degrees Celsius) and dried as well as fresh plant leaves can be used. However, when using fresh samples, the amplification yield is the highest.
Is there non-specific amplification of the amplification products?
一般由三种问题引起:1.PCR退火温度太低,循环数、引物浓度或模板浓度太高。建议提高PCR退火温度,降低PCR循环数、引物浓度或模板浓度。2.存在引物错配,建议重新设计引物。3.配制PCR反应体系时温度太高或配制完成后放置时间太久,PCR反应体系的配制在低温下进行,配制完成后尽快进行PCR扩增反应。
