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RNaseZAP™

Cleaning agent for removing RNase

Synonym(s):

RNAse cleaner, RNAse contamination remover, RNAse remover

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About This Item

UNSPSC Code:
12352200
NACRES:
NA.52

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

  • 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
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.

Legal Information

RNaseZAP is a trademark of Ambion, Inc.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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An integrative analysis of microRNA and mRNA profiling in CML stem cells
Chronic Myeloid Leukemia, 219-241 (2016)
Transcriptome analysis and RNA interference of cockroach phototransduction indicate three opsins and suggest a major role for TRPL channels.
French AS
Frontiers in Physiology, 6, 207-207 (2015)
Transport and metabolism of choline in synaptosomes: ionic requirement.
T Y Wong et al.
Biochemical Society transactions, 9(1), 84-85 (1981-02-01)
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
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