Viral DNA/RNA Isolation Kit (4x96 well)

Product#: BMG-GD2811-01
$680.00
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Viral DNA/RNA Isolation Kit (4x96 well)

Cat. No.: BMG-GD2811-01
Size: 4x96 well


Description:

EZgeneTM  96-Well blood viral DNA Kit provides an easy and reliable method for isolating total viral DNA/RNA from plasma, serum, whole blood, urine and cell culture supernatant in a 96-well format. This procedure has been tested for isolating nucleic acids from Hepatitis A, Hepatitis C and HIV. The isolated DNA/RNA can be used for PCR, RT-PCR and other downstream applications.

Applications:
  • Isolation of viral DNA and RNA from various biological sources, including:
    Plasma
    Serum
    Saliva
    Urine
    Cell culture media
    Cerebrospinal fluid
    Cellular suspensions
  • Enables rapid processing of up to 384 samples (4x96 wells) for viral detection and characterization
  • Suitable for large-scale epidemiological studies and surveillance programs
  • Preparation of viral nucleic acids for downstream diagnostic assays, such as:
    RT-PCR
    qPCR
    Real-time PCR
  • Isolation of viral genomes for:
    Next-Generation Sequencing (NGS)
    Viral genome characterization
    Mutation analysis
    Phylogenetic studies
  • Isolation of nucleic acids from various viruses, including:
    Enteroviruses
    Rhinoviruses
    Coronaviruses (including SARS-CoV-2)
    HIV
    HCV
    Influenza viruses
    Flaviviruses
    Measles virus
    Parainfluenza virus
    Parvovirus
  • Designed for use with automated liquid handling platforms, increasing throughput and reducing hands-on time
Features:
  • Isolates high-quality viral DNA and RNA
  • Yield: Up to 5 μg DNA and 10 μg RNA per well
  • Size range of isolated nucleic acids: 50 nt to ~200 kb
  • Compatible with samples stored in UTM/VTM (Universal/Viral Transport Medium)
  • Uses a single buffer system for viral particle lysis and nucleic acid adsorption
  • No organic denaturants or proteases used
  • Elution with DNase/RNase-Free Water
  • Suitable for isolating nucleic acids from a wide range of viruses
  • No post-purification DNase treatment required for most applications
  • Standardized protocol across different sample types
Reference:
Pichl, Lutz et al. “Magnetic bead technology in viral RNA and DNA extraction from plasma minipools.” Transfusion vol. 45,7 (2005): 1106-10. doi:10.1111/j.1537-2995.2005.04356.x
Lecamwasam, Ashani et al. “DNA methylation profiling of genomic DNA isolated from urine in diabetic chronic kidney disease: A pilot study.” PloS one vol. 13,2 e0190280. 20 Feb. 2018, doi:10.1371/journal.pone.0190280
 

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