CN
Magen contact QR code.png
banner
Your present location:Home/Products/DNA&RNA Purification/DNA/Plant DNA/Magnetic Kits/MagPure Seed DNA Kit
  • seed DNA extraction magnetic bead workflow plant seeds.jpg
  • plant seed genomic DNA purification GMO testing workflow.jpg

MagPure Seed DNA Kit

D6352
CAT NO PRODUCT NAME SIZE PRICE
D635201 MagPure Seed DNA Kit 48 preps $119.00
D635202 MagPure Seed DNA Kit 96 preps $224.00
D635203
MagPure Seed DNA Kit
5 x 96 preps $995.00
D6352-F-96 MagPure Seed DNA Precast Kit 96 preps $246.00
D6352-TL-06 MagPure Seed DNA Precast Kit 96 preps $246.00

Introduction

The MagPure Seed DNA Kit (D6352) is optimized for DNA extraction from seed and storage tissues, which often contain high levels of starch and storage compounds.

The workflow combines detergent-based lysis with magnetic bead purification and optimized impurity control.

Details

Workflow

Wet bead-beating seed DNA extraction workflow showing Buffer SOL disruption and lysis, lysate clarification, Buffer MPB and bead binding, optional high-molecular-weight gDNA route, and magnetic DNA purification.

Workflow Overview

The MagPure Seed DNA Kit uses a wet bead-beating magnetic workflow for purification of genomic DNA from seed samples, young leaf/fruit samples and difficult-to-grind plant or fungal tissue. Samples are disrupted and lysed in Buffer SOL using bead-beating or high-speed homogenization, followed by heat incubation and centrifugation to clarify the lysate. The DNA-containing supernatant is then combined with Buffer MPB and magnetic beads, allowing DNA to bind to the bead surface before magnetic separation, washing, drying and elution.

Sample Handling Logic

This workflow is designed for sample types where dry grinding alone may not provide consistent disruption or where wet homogenization helps simplify sample handling. Seed samples can be processed after powder preparation and wet bead-beating, while young leaf/fruit and difficult-to-grind samples can be directly homogenized with beads in Buffer SOL. For workflows requiring higher-molecular-weight genomic DNA, the kit also provides an alternative route using liquid-nitrogen grinding followed by Buffer SOL and Buffer SDS lysis. After lysate clarification, the downstream magnetic-particle purification follows a consistent bind, wash, dry and elute workflow.

Time and Workflow Characteristics

Under typical manual operation, the workflow is usually completed within about 60–80 minutes, depending mainly on seed grinding, bead-beating efficiency, lysate clarity, magnetic separation and drying control. The workflow is suitable for laboratories that need a magnetic plant DNA extraction route with flexible sample entry options, including seed-focused wet bead-beating and an alternative high-molecular-weight gDNA route. For detailed step-by-step conditions, workflow guidance and estimated processing times, please refer to the Workflow Note in the Download section.

Specifications

Features Specifications
Main Functions Isolation total DNA from 50-100 mg easy-grinded plant (tender leaf) and seed
Applications PCR, transgene detection, fluorescence quantitative PCR, southern blot, SNP site analysis, etc.
Purification technology Magnetic beads technology
Process method Manual or automatic
Sample type Conventional economic plant samples
Sample amount 50-100mg
Elution volume ≥50μl
Time per run ~60-80 minutes

Kit Contents

Contents D635201
D635202 D635203
Purification Times 48 Preps
96 Preps 5 x 96 Preps
MagPure Particles
1.7 ml
4 ml
18 ml
Buffer SOL
40 ml
90 ml
500 ml
Buffer SDS 4 ml
9 ml 50 ml
Buffer MPB 40 ml
70 ml 350 ml
Buffer GW1 26 ml
53 ml 220 ml
Elution Buffer
10 ml
30 ml
120 ml

Storage and Stability

MagPure Particles should be stored at 2-8°C upon arrival. However, short-term storage (up to 24 weeks) at room temperature (15-25°C) does not affect their performance. The remaining kit components can be stored dry at room temperature (15-25°C) and are stable for at least 18 months under these conditions.

Experiment Data



Articles

Leave A Message

Leave A Message

    Please provide us with the information below, and we'll contact you as soon as possible.

This site uses cookies to improve your online experience,allow you to share content on social media,measure traffic to this website and display customised ads based on your browsing activity.