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Romper los cuellos de botella en la extracción: Los kits de ARN de perlas magnéticas de Lingjun redefinen los estándares de eficiencia Potenciando la investigación con soluciones de ácido nucleico de alta pureza

En la investigación de biología molecular., La extracción de ARN de muestras complejas sigue siendo un cuello de botella crítico que obstaculiza la eficiencia experimental. Los métodos tradicionales luchan contra la interferencia de polisacáridos y polifenoles de las plantas, riesgos de degradación del tejido animal, and capturing trace viral nucleic acids—often being time-consuming while compromising purity and yield. With over 13 years of expertise in magnetic bead nucleic acid extraction, Shanghai Lingjun Biotechnology leverages core magnetic bead R&D capabilities to deliver a full-scene magnetic bead RNA extraction kit series, providing researchers with an efficient, safe, and stable one-stop solution.

I. Why Choose Lingjun? Core Technologies Deliver Unmatched Advantages

In-House Magnetic Bead R&D: Industry-Leading Performance

Lingjun’s self-developed superparamagnetic silica beads(1.4μm particle size, 65±5 emu/g magnetic saturation) achieve >95% nucleic acid adsorption through surface modification and functional design. Batch-to-batch consistency eliminates material variability, ensuring reproducible results across laboratories.

One-Step ProtocolRevolution: Boosts Efficiency by >50%

No centrifugation or toxic reagents: Eliminates hazardous phenol/chloroform and liquid nitrogen grinding. Room-temperature lysis with magnetic bead adsorption delivers pure RNA in under 1 hora.

Full automation compatibility: Kits adapt to mainstream nucleic acid extractors. Magnetic-rod platforms require no manual intervention, habilitando “cargar y listo” operation.

3.Conquering Four Challenging Samples: Purity Meets Top Journal Standards

Sample TypeKey InnovationPerformance (A260/A280)
Polysaccharide/polyphenol plantsProprietary lysis buffer removes impurities1.90–2.0 (dandelion leaf)
Animal tissues (muscle/liver)Grinding-free direct lysis, 100% RNA integrity1.86–1.96 (shrimp/fish liver)
Serum/plasma virusesSensitivity down to 10 IU/mL, repeatability R>0.99Full detection in gradient dilutions
Trace cellsExtraction from 0.2 µg, zero waste for rare samples32.7 μg from 20 mg pork

II. Flagship Product Matrix: Precision Solutions for Research Scenarios

Plant RNASpecialist– Polysaccharide/Polyphenol Kit

Processes challenging samples (pothos, peach trees, roses) en 30 minutos. Pre-packaged kits (96 tests/box) yield high-purity RNA (A260/A230≥1.8), >9 μg/20 mg leaves—ideal for transcriptome sequencing.

Kit de extracción de ARN total de plantas

Caso experimental:

 20mg of sweet potato leaves, peach leaves, rose leaves and eggplant leaves were extracted with LNJNBio plant total RNA extraction kit

No.MuestraA260/A280A260/A230Conc.(ng/μL)Rendimiento(μg)
120mg Sweet potato leaves1.9722.039193.7619.376
21.9762.038194.4419.444
promedio1.9742.0385194.119.41
320mg Peach leaves1.9041.477159.1615.916
41.9011.472159.5615.956
promedio1.90251.4745159.3615.936
520mg Seasonal leaves1.8551.69899.29.92
61.8581.70298.929.892
promedio1.85651.799.069.906
720mg Eggplant leaves1.9881.75298.089.808
81.9871.75598.69.86
promedio1.98751.753598.349.834

Gel electrophoresis with agarose:

Análisis de resultados: 

The A260/A280 ratio was between 1.8-2.0, while the A260/A230 ratio exceeded 1.4, indicating high purity of the extracted products. All plant leaf samples achieved nucleic acid extraction yields above 9 µg. Bright and well-integrated bands were observed in all plant leaf samples. En resumen, the extraction process yielded high-purity products with substantial output and complete electrophoretic bands when processing different plant leaf samples.

Animal RNAGuardian– Degradation-Proof Design

From shrimp to mouse tails, centrifugation-free technology ensures clear 28S/18S bands and 100% electrophoresis integrity. 50-test boxes support high-throughput labs.

Kit de extracción de ARN total de tejido animal

Caso experimental:

The total RNA extraction kit of animal tissues was used to extract shrimp meat, chicken heart, fish heart, fish liver and fish gut respectively

No.MuestraA260/A280A260/A230Conc.(de/ul)Yield(μg)
120mg de camarones1.8631.72565.485.2384
21.8651.78268.965.5168
promedio1.8641.753567.225.3776
35mg de corazón de pollo1.9581.72155.720.44576
41.9661.73656.680.45344
promedio1.9621.728556.20.4496
55mg corazón de pescado1.9441.76128.560.22848
61.9461.74227.840.22272
promedio1.9451.751528.20.2256
75mg de hígado de pescado1.9112.0791.840.73472
81.9122.06196.440.77152
promedio1.91152.065594.140.75312
910mg de intestinos de pescado1.9252.196390.723.12576
101.9282.187382.043.05632
promedio1.92652.1915386.383.09104

Gel electrophoresis with agarose:

Análisis de resultados:

The value of A260/A280 was 1.86-1.96, and the value of A260/A230 was above 1.75, which proved that the purity of the extracted product was high; different animal tissue samples had bright bands and good integrity.

Viral DetectionSharpshooter– High-Sensitivity Serum/Plasma Kit

Reliably extracts HBV/HCV nucleic acids from 200 μL samples. Delivers leading qPCR CT values for early diagnosis.

Kit de extracción de ADN sin suero/plasma

Caso experimental:

HCV nucleic acid serum standard substance was subjected to gradient dilution, and our serum/plasma virus nucleic acid extraction reagent was used to extract on the automatic nucleic acid extraction and purification instrument LJbio32H. The extracted products of various concentration gradient dilutions were subjected to qPCR detection, y los resultados son los siguientes:

dooncentration(IU/ml)CTPromedio CV
10^723.0222.9622.990.18%
10^625.8825.8325.8550.14%
10^529.0928.9729.030.29%
10^433.1632.4232.791.60%

Análisis de resultados:

 The data shows high consistency, indicating excellent sensitivity and stable reagent performance, with a correlation coefficient reaching 0.998. The extraction efficiency is remarkable, consistently detecting both low and high concentrations with stability.

All-inclusive– The Universal Total RNA Extraction Kit

The universal total RNA extraction reagent is suitable for the rapid and efficient extraction of total RNA from fresh plant, animal, hongos, cellular and other tissue samples. The whole process is convenient to operate, especially suitable for the automated nucleic acid extraction platform.The extracted and purified nucleic acids in this kit can be used for RT-PCR, Real-Time PCR, chip analysis, polyA screening, in vitro translation and molecular cloning.

The universal total RNA extraction reagent

III. Real Data, Real Impact: Client Validation Establishes Benchmark

Caso 1: An agricultural research team used the Plant DNA/RNA Dual Extraction Kit (Cat#231011) on 20 mg sweet potato leaves, logrando 775.2 ng/μL concentration (77.52 μg total yield) y 40% higher PCR efficiency.

Caso 2: CDC testing showed Lingjun’s Serum Virus Kit achieved 100% detection at 10 IU/mL—outperforming competitors (CT values 2–3 cycles earlier).

IV. Limited-Time Empowerment Program: Accelerate Your Research

Act Now – Make Extraction Anxiety-Free!

 Order online: www.lnjnbio.com

 Technical support: 18103799069 / lnjnbio@163.com

 Expo demo: Shanghai International Biotech Expo 2025 (Booth 3-B2108). Live demos + free gel reagents.

Lingjun Commitment: Unlocking nucleic acid challenges with magnetic bead power—making every extraction a trusted data foundation.

Proveedor

Shanghai Lingjun Biotecnología Co., Limitado.se estableció en 2016 que es un fabricante profesional de materiales biomagnéticos y reactivos de extracción de ácidos nucleicos..

Tenemos una rica experiencia en extracción y purificación de ácidos nucleicos., purificación de proteínas, separación celular, quimioluminiscencia, y otros campos técnicos.

Nuestros productos son ampliamente utilizados en muchos campos., como pruebas médicas, pruebas genéticas, investigación universitaria, mejoramiento genético, etcétera. No solo proporcionamos productos sino que también podemos realizar OEM, ODM, y otras necesidades. Si tienes una necesidad relacionada, no dude en contactarnos .

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