E.Z.N.A.® Universal Pathogen Kit

$0.00$231.50

• Elute in as low as 15 μL
• Prefilled Disruptor Tubes for faster sample homogenization
• No Phenol/chloroform extractions
• High-quality DNA suitable for a variety of downstream applications

D4035-00S E.Z.N.A.® Universal Pathogen Kit (Sample Request)

$0.00

The E.Z.N.A. Universal Pathogen DNA Kit allows for rapid and reliable isolation of high-quality host genomic DNA, gram-positive and gram-negative bacterial DNA, fungal spore DNA, yeast DNA, viral DNA and viral RNA from tissues, blood, urine, serum, whole blood, and stool samples.

This kit incorporates Omega Bio-tek’s Disruptor Tubes prefilled with glass beads for faster and easier processing. The Disruptor Tubes allow for simultaneous homogenization and lysis of the samples and aid in the effective disruption of difficult samples. No detergents are present in the initial lysis buffer, which eliminates foaming issues and provides optimal conditions for homogenization.

This unique buffer system does not require alcohol to bind nucleic acids, allowing for the recovery of high-quality DNA/RNA free of PCR inhibitors. Omega Bio-tek’s MicroElute LE Spin Columns are used, which support elution volumes as low as 15 μL to obtain a high concentration of the eluate.

For Research Use Only. Not for use in diagnostic procedures.

FEATURESSPECIFICATIONS
Starting Amount25-30 mg tissue, 250 µL fecal sample / serum / urine/blood,
Starting Materialtissue, urine, serum, and fecal sample
Elution Volume15-100 μL
TechnologySilica MicroElute spin column
Processing ModeManual, Centrifugation/Vacuum
NoteHost genomic DNA, gram positive and negative bacterial DNA, fungal spore DNA, and viral DNA and RNA
ITEMAVAILABLE SEPARATELY
Disruptor TubesView Product
MicroElute® LE DNA ColumnsView Product
2 mL Collection Tubes
SLX-Mlus BufferView Product
DS BufferCall for Pricing
PCP Buffer
RBB BufferView Product
HBC BufferView Product
DNA Wash BufferView Product
Elution BufferView Product
Proteinase K SolutionView Product

Figure 1. Human fecal samples suspended in PBS solution were spiked into corresponding organisms. Fecal samples were then processed according to each manufacturer’s recommended protocols. qPCR was performed in triplicate for each sample using primers specific for the target organism. Data shown are averages on triplicate reactions.

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