Innovative Magnetic Grain Modern Technology Delivers Superior RNA Purity, Return, and Effectiveness for Molecular Study.
Shanghai, China– [15th July]– Lnjnbio (Shanghai Lingjun Biotechnology Co., Ltd.), a leading supplier of sophisticated life science research study remedies, is honored to announce the release of its Magnetic Grains for Pet Cells Total RNA Removal Kit. This sophisticated set is designed to enhance the seclusion of top notch overall RNA from a vast array of animal tissues, supplying scientists an efficient, reliable, and automation-friendly alternative to traditional column-based and phenol-chloroform removal methods.
Revolutionizing RNA Extraction with Magnetic Grain Technology
The Lnjnbio Magnetic Beads for Animal Tissue Total RNA Removal Package employs an exclusive magnetic bead-based filtration system that makes certain rapid, high-purity RNA isolation with minimal hands-on time. By leveraging maximized surface chemistry and magnetic separation, this package gets rid of the need for centrifugation, vacuum filtering, or harmful natural solvents, dramatically decreasing processing time while taking full advantage of RNA stability.
(Lnjnbio Magnetic Beads for Animal Tissue Total RNA Extraction Kit)
Secret Features & Advantages
Extraordinary RNA Pureness & Return
Exclusive magnetic beads uniquely bind RNA while properly getting rid of pollutants such as proteins, genomic DNA, and enzymatic preventions.
A260/A280 proportions constantly ≥ 1.9, making certain ideal pureness for downstream applications like NGS and qPCR.
Rapid & User-Friendly Workflow
Complete removal in as little as 20– 30 minutes, a significant improvement over traditional approaches.
No centrifugation or column transfers called for– merely mix, bind, clean, and elute.
Efficient lysis barrier system guarantees full tissue disturbance even for coarse or lipid-rich examples.
Automation-Ready for High-Throughput Labs
Completely suitable with fluid handling robots (e.g., KingFisher, Biomek, Tecan) for seamless assimilation into automated workflows.
Suitable for large genomic researches, professional research study, and industrial applications.
( Electropherogram of Lnjnbio Magnetic Beads)
Dynamic Binding Capability: As Much As 50 µg RNA per mg of grains, suiting a large range of input cells weights (10– 50 mg).
RNase-Free Guarantee: All elements are rigorously tested to avoid RNA deterioration.
Technical Emphasizes
1. Superior Magnetic Grain Efficiency
Bead Make-up: High-capacity silica-coated magnetic particles with consistent size (1– 3 µm) ensure consistent RNA binding performance.
Dynamic Binding Capability: As Much As 50 µg RNA per mg of beads, fitting a large range of input cells weights (10– 50 mg).
RNase-Free Assurance: All components are rigorously evaluated to stop RNA deterioration.
2. Maximized Buffer System
Lysis Barrier: Rapidly interrupts cells while stabilizing RNA, even in RNase-rich atmospheres.
Laundry Buffers: Successfully get rid of impurities without jeopardizing RNA yield.
Elution Barrier: Low-EDTA formulation makes certain compatibility with sensitive downstream assays.
3. Extensive Quality Control
Each batch goes through endotoxin testing, DNase/RNase recognition, and efficiency benchmarking against industry criteria.
Guaranteed > 90% undamaged RNA (RIN ≥ 8.0) for demanding applications like single-cell sequencing.
Provider Intro
Shanghai Lingjun Biotechnology Co., Ltd. was established in 2016 and is a specialist supplier of biomagnetic materials and nucleic acid removal reagents.
We have rich experience in nucleic acid removal and filtration, healthy protein filtration, cell separation, chemiluminescence and various other technical areas.
Our products are widely used in many fields, such as medical testing, genetic testing, university research, genetic breeding, and so on. We not only provide products but can also undertake OEM, ODM, and other needs. If you have related needs about dna isolation and extraction, please feel free to contact us at sales01@lingjunbio.com.
All articles and pictures are from the Internet. If there are any copyright issues, please contact us in time to delete.
Inquiry us