Pre-processing of bacterial sample genomic DNA extraction 96 Samples

$225.00

Dostava USD 45 - Besplatno preko USD 300

DTE je kineska platforma za e-trgovinu specijalizirana za online prodaju molekularnog testiranja, ELISA, i srodni proizvodi.

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Opis

Instructions:

  1. Sample Collection:
    • Collect 0.1-1ml blood sample.
  2. Priprema uzorka:
    • Dodati 2 to 3 times the volume of 1x red blood cell solution to the blood sample.
    • Mix thoroughly by inverting.
    • Centrifuge at 12,000 rpm for 1 minute.
    • Carefully aspirate the supernatant. The precipitate should ideally be white or light red.
    • Dodati 400 μl reagent buffer I and 10 μl epoxy resin K (10 mg/ml) to the precipitate.
    • Vortex and mix for 15 sekundi, then let it sit for 2 minuta.
  3. Special Case: Low-level Organisms:
    • If processing blood from low-level organisms (e.g., poultry, birds) containing cell nuclei:
    • Add 1x red blood cell solution and directly add 200 μl of reagent buffer I (total volume not exceeding 500 μl).
    • Let it sit for 2 minuta.
  4. Digestion:
    • Dodati 10 μl epoxy resin K (10 mg/ml) to the mixture.
    • Invert and mix, then digest at 65°C for 10 minuta.
    • During this period, invert and mix 6-7 times to ensure complete digestion.
  5. Transfer to Reagent Plate:
    • Add the solution from the previous step to the 96-well reagent plate.
    • Follow specific steps outlined in the automatic extraction protocol for further processing.

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Težina0.7 kg
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