NucleoSpin RNA

NucleoSpin RNA

Brand: MACHEREY-NAGEL
In stock
SKU
NucleoSpin RNA
Grouped product items
Product Name Size
NucleoSpin® RNA
SKU: 740955.10
10 Preps
NucleoSpin® RNA
SKU: 740955.50
50 Preps
NucleoSpin® RNA
SKU: 740955.250
250 Preps
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NucleoSpin RNA
NucleoSpin RNA

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Applications

  • RNA isolation from cultured cells, tissue (standard protocol)
  • RNA from < 109 bacterial cells (Gram-negative, Gram-positive) or < 108 yeast cells
  • RNA from ≤ 100 μL biological fluids
  • RNA clean-up from reaction mixtures
  • RNA from samples stored in RNAlater®
  • RNA from saliva samples collected with Oragene®•RNA (Genotek)
  • Typical downstream applications: real-time RT-PCR, Northern blotting, primer extension, array technology, RNase protection assays

Features

  • rDNase included for on-column DNA digestion– easy and efficient removal of contaminating DNA
  • NucleoSpin® Filters (shredders) – efficient sample homogenization and reduction of viscosity
  • Up to 70 μg ready to use RNA
  • Parallel purification of genomic DNA by using the NucleoSpin® RNA/DNA Buffer Set

Specifications

  • Technology: Silica membrane technology
  • Fragment size: > 200 nt
  • A260/A280: 1.9–2.1
  • Processing: Centrifugation
  • Sample material: Cultured cells (< 5 x 10⁶) bacterial cells (< 10⁹), yeast cells (< 10⁸) Human / animal tissue (< 30 mg)
  • Typical yield: HeLa cells (10⁶): 14 μg, bacterial cells (10⁹): 70 μg
  • Elution volume: 30–120 μL
  • Binding capacity: 200 μg
  • Processing time: 35 min/6 preps

NucleoSpin RNA II procedure

NucleoSpin RNA II procedure

NucleoSpin RNA II procedure.

Residual Genomic DNA Comparison on an Agarose Gel

Residual Genomic DNA Comparison on an Agarose Gel

Residual Genomic DNA Comparison on an Agarose Gel. 10 μl of each eluate was treated with RNase A and subsequently loaded onto a 1% TAE agarose gel to reveal any contaminating genomic DNA.The NucleoSpin RNA II kit contains DNase I for on-column digestion. For Competitor Q’s kit, an additional on-column DNA digestion set was purchased separately in order to perform the digest. Lane M: λ/HindIII DNA size marker. Note: Optimized DNase I treatment has eliminated genomic DNA in total RNA samples purified with the NucleoSpin RNA II kit. Even after DNA digestion, Competitor Q’s kit showed evidence of genomic DNA contamination.

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Applications

  • RNA isolation from cultured cells, tissue (standard protocol)
  • RNA from < 109 bacterial cells (Gram-negative, Gram-positive) or < 108 yeast cells
  • RNA from ≤ 100 μL biological fluids
  • RNA clean-up from reaction mixtures
  • RNA from samples stored in RNAlater®
  • RNA from saliva samples collected with Oragene®•RNA (Genotek)
  • Typical downstream applications: real-time RT-PCR, Northern blotting, primer extension, array technology, RNase protection assays

Features

  • rDNase included for on-column DNA digestion– easy and efficient removal of contaminating DNA
  • NucleoSpin® Filters (shredders) – efficient sample homogenization and reduction of viscosity
  • Up to 70 μg ready to use RNA
  • Parallel purification of genomic DNA by using the NucleoSpin® RNA/DNA Buffer Set

Specifications

  • Technology: Silica membrane technology
  • Fragment size: > 200 nt
  • A260/A280: 1.9–2.1
  • Processing: Centrifugation
  • Sample material: Cultured cells (< 5 x 10⁶) bacterial cells (< 10⁹), yeast cells (< 10⁸) Human / animal tissue (< 30 mg)
  • Typical yield: HeLa cells (10⁶): 14 μg, bacterial cells (10⁹): 70 μg
  • Elution volume: 30–120 μL
  • Binding capacity: 200 μg
  • Processing time: 35 min/6 preps

NucleoSpin RNA II procedure

NucleoSpin RNA II procedure

NucleoSpin RNA II procedure.

Residual Genomic DNA Comparison on an Agarose Gel

Residual Genomic DNA Comparison on an Agarose Gel

Residual Genomic DNA Comparison on an Agarose Gel. 10 μl of each eluate was treated with RNase A and subsequently loaded onto a 1% TAE agarose gel to reveal any contaminating genomic DNA.The NucleoSpin RNA II kit contains DNase I for on-column digestion. For Competitor Q’s kit, an additional on-column DNA digestion set was purchased separately in order to perform the digest. Lane M: λ/HindIII DNA size marker. Note: Optimized DNase I treatment has eliminated genomic DNA in total RNA samples purified with the NucleoSpin RNA II kit. Even after DNA digestion, Competitor Q’s kit showed evidence of genomic DNA contamination.

Write Your Own Review
You're reviewing:NucleoSpin RNA
Your Rating