Quality Level
form
liquid
feature
RNase free (removal from glass and plastic surfaces)
packaging
pkg of 250 mL
technique(s)
RNA purification: suitable
pH
7.0-7.4
transition temp
flash point 100 °C (closed cup)
solubility
water: soluble
density
1000 g/cm3
General description
RNaseZAP™ is a purifying agent used for eliminating RNase contamination from glassware, plastic surfaces, reaction vessels, countertops and pipettors. It is also used for effective removal of RNase residues from microcentrifuge tubes without inhibiting subsequent enzymatic reactions.
Application
A cleaning agent for removing RNase from glassware, plastic surfaces, countertops, and pipettors. It is also effective at eliminating RNase contamination from microcentrifuge tubes without inhibiting subsequent enzymatic reactions.
- RNaseZAP™ has been used as a cleaning agent for removing RNase from glassware, apparatus, countertops and pipettors.
- Remove RNase contamination from glass and plastic surfaces
- CAUTION: Please note that RNaseZap Solution should not be used on corrodible metal surfaces
Legal Information
RNaseZAP is a trademark of Ambion, Inc.
저장 등급
12 - Non Combustible Liquids
문서
SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.
Learn how water impurities can affect DNA and RNA electrophoresis and blotting. High purity water purified using ultrafiltration is suitable for nucleic acid electrophoresis, Northern and Southern blotting.
관련 콘텐츠
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Instructions
Sandra Nwokeoha et al.
Ultrasound in medicine & biology, 42(10), 2478-2492 (2016-07-23)
The delivery of genes into cells through the transfer of ribonucleic acids (RNAs) has been found to cause a change in the level of target protein expression. RNA-based transfection is conceptually more efficient than commonly delivered plasmid DNA because it
Farah J Nassar et al.
Methods in molecular biology (Clifton, N.J.), 1465, 219-241 (2016-09-02)
Integrative analysis of microRNA (miRNA) and messenger RNA (mRNA) in Chronic Myeloid leukemia (CML) stem cells is an important technique to study the involvement of miRNA and their targets in CML stem cells self-renewal, maintenance, and therapeutic resistance. Here, we
Transport and metabolism of choline in synaptosomes: ionic requirement.
T Y Wong et al.
Biochemical Society transactions, 9(1), 84-85 (1981-02-01)