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NucleoSpin Soil, Mini Kit für DNA aus Bodenproben

NucleoSpin Soil ist die Lösung für die Aufreinigung von DNA aus Bodenproben. Die Homogenisierung der Proben kann mit den mitgelieferten MN Bead Tubes Typ A durchgeführt werden. Zwei spezielle Lysepuffer, die für unterschiedliche Bodenzusammensetzungen geeignet sind, und der Enhancer SX sorgen für die Lyse der Bodenprobe. Die NucleoSpin Inhibitor Removal Column gewährleistet die Entfernung von störenden Substanzen, bevor die DNA in einem einfachen Workflow extrahiert wird.

Anwendung Isolierung von DNA
Automatische Nutzung Nein
CE-zertifiziert Nein, nur für wissenschaftlichen Gebrauch
Elutionsvolumen 30–100 µL
Format Mini Präp
Fragmentgröße 50 bp–ca. 50 kbp
Gefahrstoffe Ja
Haltbarkeit (ab Produktion) 27 Monat(e)
Handhabung Zentrifugation
Lagertemperatur 15–25 °C
Lysat-Klärung NucleoSpin Säule zur Entfernung von Inhibitoren, Zentrifugation
Präparationszeit 90 min/10 Präps
Probenmaterial Boden, Schlamm, Sediment
Probenmenge < 500 mg
Technologie Silica-Membrantechnologie
Theoretische Bindungskapazität 50 µg
Typische Ausbeute 2-10 µg (500 mg Boden)
Typische Downstream-Anwendung Echtzeit-PCR, Microarrays, PCR, Southern Blotting
Verkaufseinheit 10 Präp(s), 50 Präp(s), 250 Präp(s)
Warenzeichen NucleoSpin
Ziel DNA

NucleoSpin Soil

Soil samples contain different amounts of organic matter and inorganic material (humic substances or polysaccharides) and exhibit different phs, all of which can hinder the consistency of DNA extraction from these sample types. The NucleoSpin Soil kit overcomes these obstacles though the use of highly optimized lysis conditions and mechanical disruption.

NucleoSpin Soil procedure

Superior DNA yield and purity from various soil types

Two different lysis buffer options plus optional addition of the chemical additive Enhancer SX allow fine tuning for maximum yield and purity.

Complete removal of PCR inhibitors – PCR results even from undiluted eluates! 

DNA was purified with NucleoSpin Soil using Lysis Buffer SL1 and Lysis Buffer SL2 with, and without. Enhancer SX as well as with kits from competitor MP, and MO. Then, 2 μL of undiluted eluate were used as PCR template with fungi specific internal transcribed spacer (ITS) primers. Competitor MP failed to yield DNA pure enough to be used undiluted. DNA, and inhibitor concentration were both low for competitor MO, but the PCR from river sediment samples was still strongly inhibited. With NucleoSpin Soil there were at least two conditions for each soil type yielding plenty of DNA, and working undiluted in PCR.

Efficient lysis system – even suitable for difficult-to-lyse microorganisms

Total DNA from 400 mg cropping soil was purified with NucleoSpin Soil using Lysis Buffer SL2 in combination with Enhancer SX. 2 μl of undiluted eluates were analyzed in PCR using, order specific primer systems.

Selected citations

Adamczyk et al. Plant roots increase both decomposition, and stable, organic matter formation in boreal forest soil. Nature Communications, volume 10, 3982 (2019). 

Goncalves et al. Microbiota stimulation generates LCMV-specific memory CD8+ T cells in SPF mice, and determines their TCR repertoire during LCMV infection. Molecular Immunology, volume 124, pages 125–141 (2020).

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