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DNA/RNA Shield (50 ml)Cat#: R1100-50DNA/RNA Shield reagent is a DNA and RNA stabilization solution for nucleic acids in any biological sample. This DNA and RNA stabilization solution preserves the...
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Format
Quick-RNA MagBead
Highlights
- Versatile: High-throughput, magnetic bead-based isolation total RNA (including small/micro RNAs) from any sample including cells, solid tissue, whole blood, biological liquids, FFPE tissue, environmental (plant/seed), swabs (stool, soil, microbial samples), etc.
- NGS-Ready: High-quality RNA is ready for any downstream application. DNase I included.
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Cat # | Name | Size |
---|
Cat # | Name | Size | |
---|---|---|---|
C2007-8 | 96-Well Plate Cover Foil | 8 Foils | |
C2002 | Collection Plate | 2 Plates | |
C2003 | Elution Plate | 2 Plates | |
P1005 | ZR-96 MagStand | 1 | |
C2007-2 | 96-Well Plate Cover Foil | 2 Foils | |
C2007-4 | 96-Well Plate Cover Foil | 4 Foils | |
R1200-25 | DNA/RNA Shield (2X Concentrate) | 25 ml | |
R1200-125 | DNA/RNA Shield (2X Concentrate) | 125 ml | |
D3001-2-5 | Proteinase K w/ Storage Buffer Set | 5 mg | |
D3001-2-20 | Proteinase K w/ Storage Buffer Set | 20 mg | |
W1001-4 | DNase/RNase-Free Water | 4 ml | |
W1001-6 | DNase/RNase-Free Water | 6 ml | |
W1001-10 | DNase/RNase-Free Water | 10 ml | |
W1001-30 | DNase/RNase-Free Water | 30 ml | |
W1001-1 | DNase/RNase-Free Water | 1 ml | |
D4100-2-12 | |||
D4100-2-24 | MagBinding Beads | 24 ml | |
D4100-2-3 | |||
R1060-1-100 | RNA Lysis Buffer | 100 ml | |
R1060-1-50 | RNA Lysis Buffer | 50 ml | |
E1010 | DNase I Set | 250 U | |
R1060-2-50 | RNA Prep Buffer | 50 ml | |
R2130-1-120 | |||
R2130-1-30 | |||
R2130-2-20 | |||
R2130-2-80 | |||
R1060-2-100 | RNA Prep Buffer | 100 ml | |
Description
Performance
Technical Specifications
Binding Capacity | 15 µg total RNA per 30 µl MagBinding Beads. |
---|---|
Equipment Needed | Magnetic stand or separator, heat block, liquid handler or robotic sample processor (user provided). |
Purity | High-quality RNA is ready for Next-Gen Sequencing, RT/PCR, hybridization, etc. |
Recommended Materials | (available separately) – 96-well Collection Plate (C2002; capacity is up to 1.2 ml/well), 96-Well Block (P1001; capacity is up to 2 ml/well), 96-well Elution Plate (C2003), Cover Foil (C2007), ZR-96 MagStand (P1005). |
Sample Preservation | DNA/RNA Shield lyses cells, inactivates nucleases and infectious agents and is ideal for safe sample storage and transport at ambient temperatures (page 7). |
Sample Sources | Any cells, solid tissue, whole blood, biological fluids, FFPE tissue, environmental (plant/seed), swabs (stool, soil, microbial samples), samples stored in DNA/RNA Shield, etc. |
Size Limits | Total RNA including small/microRNAs ≥ 17nt. |
Storage | RNA eluted with DNase/RNase-Free Water (provided) can be stored frozen. The addition of RNase inhibitors is highly recommended for prolonged storage. |
Resources
Documents
FAQ
Input | Average RNA Yield |
---|---|
Cells | 10 µg (per 106 cells) |
HeLa | 15 µg |
High Yield Tissue (mouse) | ≥ 30 µg (per 10 mg) |
Spleen | 30-50 µg |
Liver | 40-60 µg |
Low Yield Tissue (mouse) | ≤ 30 µg (per 10 mg) |
Brain, Heart | 5-15 µg |
Muscle | 5-20 µg |
Lung | 10-20 µg |
Intestine | 10-30 µg |
Kidney | 20-30 µg |
Whole Blood | (per 1 ml) |
Porcine | 10-20 µg |
Human | 2-10 µg |
Purity, RIN and/or any type of contamination can result from initial sample preparation (i.e., inefficient lysis of the sample). To improve, increase the volume of the lysis reagent (e.g., TRI Reagent/TRIzol or RNA Lysis Buffer).
- To ensure complete lysis, increase the volume of the lysis reagent (i.e., increase or titrate the volume of TRI Reagent/TRIzol or RNA Lysis Buffer). Lysate should be clear (not opaque or viscous). Pellet debris by centrifugation (if needed) and process the cleared supernatant.
- Prior to adding TRI Reagent/TRIzol or RNA Lysis Buffer, perform enzymatic treatment (Proteinase K; #D3001-2-20) and/or mechanical homogenization (bead beating with ZR BashingBead Lysis Tubes; #S6003) in DNA/RNA Shield (#R1100).
This can happen on occasion due to transport or storage at lower temperatures. The reagent functionality is not affected; however, the precipitate can be resolved by heating the reagent to >37 °C.
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