Description 

1X Tris-Glycine-SDS Running Buffer Powder is used for electrophoresis on Q-PAGE™ TGN Precast Gel or Laemmli Tris-HCl gels in Tris-Glycine buffer system. It is convenient and universal for electrophoresis in Tris-Glycine buffer system.

Features

• Reliable: Rigorous quality control for reproducible separation of protein electrophoresis.

• Convenient: Premeasured pouches make 1 liter of 1X buffer solution; No pH adjustment is necessary. 

• Fast: Dissolving in minutes and then ready to use.

• Stable: Powder packaging suitable for long-term storage.

Contents 

0.025 M Tris, 0.192 M glycine, 0.10% SDS

Applications 

Running buffer for Laemmli Tris-HCl gel electrophoresis

Storage

Room temperature for 24 months 

1X Tris-Glycine-SDS Running Buffer Powder is used for electrophoresis on Q-PAGE™ TGN Precast Gel or Laemmli Tris-HCl gels in Tris-Glycine buffer system. It is convenient and universal for electrophoresis in Tris-Glycine buffer system.

bis-PEG4-endo-BCN is a homobifunctional click chemistry linker, PEG increase its aqueous solubility. The BCN group enable copper free click chemitry with azide-tagged molecules. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

bis-PEG4-endo-BCN is a homobifunctional click chemistry linker, PEG increase its aqueous solubility. The BCN group enable copper free click chemitry with azide-tagged molecules. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

Introduction

This product speeds and simplifies nucleic acid size selection for fragment library preparation for next generation sequencing.

Details

Specifications

Features	Specifications
Main Functions	Selectively recover DNA from PCR products and enzymatic reaction solution （Replace Beckmen or agencourt SPRISelect）
Applications	Prepare DNA library for second generation sequencing
Purification technology	Magnetic beads technology
Process method	Manual or automatic
Sample type	DNA products, restriction endonuclease systems, or other enzymatic reaction solution
Sample amount	Appropriate
Recovery	80%
Operation time	≤50 minutes

Principle

The MagSelect method contains magnetic particles in an optimized binding buffer to selectively bind DNA fragments 100bp and larger to paramagnetic beads. Excessprimers, nucleotides, salts, and enzymes can be removed using a simple washing procedure. The result is a more purified PCR product.

Advantages

• High recovery – up to 80%
• High throughput – using magnetic beads purification technology

Kit Contents

Contents	XP-5	XP-50	XP-500
MagSelect Beads	5 ml	50 ml	500 ml

Storage and Stability

MagSelect XP should be stored at 2-8°C upon arrival and is stable up to 18 months under the condition. However, short-term storage (up to 12 weeks) at room temperature (15-25°C) does not affect its performance. Shake the reagent well before use. It should appear homogenous and consistent in color.

DO NOT FREEZE.

This product speeds and simplifies nucleic acid size selection for fragment library preparation for next generation sequencing.