Viral Nucleic Acid Extraction Kit

Suitable for extract viral DNA or viral RNA from various bodily fluid samples.

Viral Nucleic Acid Extraction Kit

  • Preparate viral nucleic acid within 20-40 min.
  • Detection sensitivity of viral DNA is increased 10-50 timesthan the boiling extraction
  • Detection sensitivity of viral RNA is increased 5-10 timesthan the traditional Trizol method.
  • Carrier RNA increases the detection sensitivity (stable detection of virus at a concentration of 100 copies/ml in body fluids).
  • No need of phenol chloroform and isopropanol.
  • Nucleic acids are free of impurities and inhibitors and can be amplified using up to 1/2 the PCR reaction volume as

Price List

Product No Quantity Price
4002050 50 preps contact us
4002250 250 preps contact us

Description

The body fluid sample is digested by proteinase K to release viral nucleic acid, and then supplemented by column purification technology to adsorb viral nucleic acid on the spin column. After washing the spin column with a wash buffer, the impurities and PCR inhibitors remaining on the spin column can be completely removed. Viral nucleic acids on the spin column can be eluted directly with Buffer TE and can be used directly in various molecular biology experiments.

Specifications

  • Samples: body fluids (plasma, serum, urine, CSF, and cell culture supernatant).
  • Sample amount: 200 μl body fluid sample.

Experimental date

Figure 1: Amplification plot of HBV DNA

Curve 1: Nucleic acids extracted in serum by boiling method (5 μl DNA added in a 50 μl amplification system).

Curve 2: Nucleic acids extracted from the same serum (200 μl) with Simgen Virus Nucleic Acid Extraction Kit (5 μl DNA added in a 50 μl amplification system).

Curve 3: Nucleic acids extracted from the same serum (200 μl) with Simgen Virus Nucleic Acid Extraction Kit (25 μl DNA added in a 50 μl amplification system). No significant inhibition effect was observed, but the CT value was reduced.

Specifications

Resources

Thesis

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  2. YangH, Liang W, Si J, et al. Long spacer arm-functionalized magnetic nanoparticle platform for enhanced chemiluminescent detection of hepatitis B virus[J]. Journal of Biomedical Nanotechnology, 2014, 10(12): 3610-3619.
  3. Zhou C, Jin X, Tang J, et al. Association of CD40-1C/T polymorphism in the 5′-untranslated region with chronic HBV infection[J]. Cellular Physiology and Biochemistry, 2015, 35(1): 83-91.
  4. Ali Z, Liang W, Jin L, et al. Development of magnetic nanoparticles based nucleic acid extraction method and application in hepatitis c virus chemiluminescent detection[J]. Science of Advanced Materials, 2015, 7(7): 1233-1240.
  5. 王海萍, 陈秀丽, 周朱瑛, 等. 肠道病毒 71 型脑炎患儿血清和脑脊液 CD 40, CD 40 L 和血管细胞黏附分子-1 检测的价值[J]. 疾病监测, 2015, 30(7): 534-538.
  6. YangH, Guo Y, Li S, et al. Magnetic beads-based chemiluminescent assay for ultrasensitive detection of pseudorabies virus[J]. Journal of Nanoscience and Nanotechnology, 2014, 14(5): 3337-3342.
  7. Zhang Q, Li S, Lei P, et al. ANXA2 Facilitates Enterovirus 71 Infection by Interacting with 3D Polymerase and PI4KB to Assist the Assembly of Replication Organelles[J]. Virologica Sinica, 2021, 36(6): 1387-1399.
  8. Liu X, Liang J, Yu Y, et al. Discovery of aryl benzoyl hydrazide derivatives as novel potent broad-spectrum inhibitors of influenza A virus RNA-dependent RNA polymerase (RdRp)[J]. Journal of Medicinal Chemistry, 2022, 65(5): 3814-3832.
  9. Liu X, Xu Z, Liang J, et al. Identification of a novel acylthiourea-based potent broad-spectrum inhibitor for enterovirus 3D polymerase in vitro and in vivo[J]. Antiviral Research, 2023, 213: 105583.
  10. Ren J, Yu L, Zhang Q, et al. AIMP2 restricts EV71 replication by recruiting SMURF2 to promote the degradation of 3D polymerase[J]. Virologica Sinica, 2024.
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