Kit de extração de DNA/RNA total (método de coluna de rotação) para teste de vírus de aves

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Catalog No.: DP201-01 / DP201-02
Specifications: 25T / 50T
Storage: Room Temperature (15–25°C)

Product Description

The Total DNA/RNA Extraction Kit is designed for rapid and efficient purification of high-quality total nucleic acids—including viral, bacterial, and parasitic DNA/RNA—from a variety of biological samples such as tissues, blood, secretions, and excreta.

Utilizing silica membrane spin column technology, the kit enables reliable nucleic acid extraction without the need for toxic phenol-chloroform or time-consuming alcohol precipitation. The purified nucleic acids are suitable for a wide range of downstream applications, including PCR, RT-PCR, LAMP/RT-LAMP, and Southern/Northern blotting.


Principle of the Method

Under high-salt conditions, nucleic acids bind selectively to the silica membrane in the spin column, while proteins and impurities are washed away. After multiple wash steps, high-purity DNA/RNA is eluted using DEPC-treated water, ready for immediate use in molecular biology workflows.


Kit Contents

ComponentDP201-01 (25T)DP201-02 (50T)Storage
Lysis Buffer15 mL30 mLRT
Wash Buffer5 mL10 mLRT
Elution Buffer5 mL10 mLRT
Spin Columns (Tube A)25 pcs50 pcsRT
Collection Tubes (B)25 pcs50 pcsRT

⚠️ Note: Add 20 mL (for 25T) ou 40 mL (for 50T) of absolute ethanol to the Wash Buffer before first use.


Sample Types & Preparation

  • Sangue: Centrifuge >500 µL EDTA-anticoagulated blood, transfer 200 µL of plasma for extraction.

  • Tecido: Homogenize 0.05–1 g tissue in saline (5–10× volume), take 200 µL homogenate for processing.

  • Swab/Fecal Samples: Swab the collection area after moistening in saline. Detach the swab tip into a 1 mL saline tube, vortex 30 sec, then transfer 200 µL.


Simplified Protocol of The Extraction Kit

  1. Mix 200 µL sample with 500 µL lysis buffer → incubate 5 min → centrifuge.

  2. Transfer 400 µL supernatant + 200 µL ethanol → vortex.

  3. Load onto Spin Column A (in Collection Tube B) → centrifuge 1 min.

  4. Discard flowthrough → add 600 µL wash buffer → centrifuge 1 min.

  5. Repeat centrifugation to dry column → transfer Column A to a new tube.

  6. Add 50 µL elution buffer → incubate 1–2 min → centrifuge → collect nucleic acids.

⏱️ Total time: ~20–30 minutes
🧊 Storage of purified nucleic acids: Store at -80°C if not used immediately.


Precautions

  • For single use only; do not reuse spin columns or collection tubes.

  • Wear gloves, a lab coat, and a mask during the operation. Avoid touching tube rims and column openings.

  • Disinfect work surfaces and equipment after use with 1% sodium hypochlorite or 75% ethanol.

  • Dispose of biological waste in accordance with safety regulations.


Applications of This Total DNA/RNA Extraction Kit

  • Viral and bacterial nucleic acid extraction

  • Avian diagnostic sample preparation

  • PCR, RT-PCR, and isothermal amplification

  • Veterinary diagnostics and research labs


Ordering Information

Product CodeFormatSample CapacityStorage
DP201-0125 TestsFor small to mid-scale useRoom Temperature
DP201-0250 TestsFor high-throughput labsRoom Temperature

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