Direct Extraction Buffer

For general laboratory use.

Please centrifuge briefly before opening (volume ≤2 ml).

Shipping: shipped at ambient temperature

Storage Conditions: store at 4°C or -20°C

Shelf Life: 12 months

Form: liquid

Concentration: 10 x

Description:
Direct Extraction Buffer allows an easy and fast extraction of DNA and RNA directly from blood, swabs and animal- or plant tissue. The buffer is optimized for use in combination with Direct PCR or RT-PCR master mixes like qPCR ProbesMaster (PCR-396) or SCRIPT Direct RT-qPCR ProbesMaster (PCR-528).

The mix allows DNA and RNA preparation within 3-5 minutes and with a minimum of pipetting steps. It is especially recommended for:

• Direct detection of viral or bacterial DNA in nasal or throat swabs
• Direct PCR from blood samples
• Direct amplification of target DNA from various tissue samples
• Point-of-Care diagnostics

The preparation process can be easily automatized.

Content:
Direct Extraction Buffer
10 x conc.

Sample preparation
a) Blood Samples / Liquid Samples

• Dilute 10x Extraction Buffer to 1x concentrated Buffer with PCR-grade water.
• Transfer 2 μl of the Blood/Liquid Sample into a tube containing 100 μl to 200 μl of 1x concentrated Extraction Buffer (a dilution of Blood 1:50 to 1:100 in 1x Extraction Buffer is recommended).
• Close the tube and vortex for 15 sec
• Incubate the tube at room temperature (20-25 °C) for 2-3 min.
• Transfer 1-2 μl of the supernatant into a 20 μl qPCR assay or 2-5 μl into a 50 μl qPCR assay.

b) Samples from nasal or throat swabs

• Dilute 10x Extraction Buffer to 1x concentrated Buffer with PCR-grade water.
• Transfer 200 μl 1x Extraction Buffer into a 1.5 ml microtube
• Cut off the cotton tip with the collected nasal or throat swab and place it in the micro tube
• Close the tube and vortex for 15 sec
• Incubate at room temperature (20-25 °C) for 2-3 min
• Remove the cotton tip and squeeze it out at the rim of the tube
• Centrifuge briefly and transfer 1-2 μl of the supernatant into a 20 μl qPCR assay or 2-5 μl into a 50 μl qPCR assay.

c) Samples from Animal or Plant Tissue

• Dilute 10 x Extraction Buffer to 1 x concentrated Buffer with PCR-grade water.
• Prepare a small piece from animal or plant tissue not exceeding 8 mm in diameter
• Crack plant seeds to less than 1 mm in diameter using a BeadBeater, Tissue Lyser or small hammer
• Place the sample in a 1.5 ml microtube
• Add 1x concentrated Extraction Buffer to the tissue sample as following:

• Mix briefly by tapping or vortexing and make sure that the sample is

  10x Extraction Buffer

  Hazard pictograms:
  

  
  
  Corrosion

  Signal word: Danger

  Hazard statements:
  H314 Causes severe skin burns and eye damage.

  Precautionary statements:
  P260 Do not breathe dust/fume/gas/mist/vapours/spray.
  P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/....
  P303 + P361 + P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower].
  P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
  P310 Immediately call a POISON CENTER/doctor/....
  P321 Specific treatment (see ... on this label). soaked with Extraction Buffer

• Incubate at room temperature (20-25 °C) for 3 min
• Centrifuge briefly and transfer 1-2 μl of the supernatant into a 20 μl qPCR assay or 2-5 μl into a 50 μl qPCR assay.