form
dry powder (dehydrated (DCM))
manufacturer/tradename
Anaerocult™
bulk density
550 kg/m3
suitability
suitable for microbiology, anaerobic bacteria
application(s)
food and beverages
microbiology
storage temp.
−20°C
General description
ANAEROCULT™ IS contains components that chemically bind any oxygen present within a short space of time and release carbon dioxide thus creating an anaerobic atmosphere. The special incubation bag is designed to accommodate all identification galleries currently on the market.
for microbiology Gas generator system for the anaerobic incubation of identification systems and sensitivity tests
Application
ANAEROCULT™ IS gas generating system is used for the anaerobic incubation of identification systems and susceptibility test. Each item for incubation can be evaluated without disrupting the anaerobic conditions. Results that are initially unclear can be checked repeatedly without having to open the incubation bag.
Analysis Note
Growth
- Bacteroides fragilis ATCC 25285
passes test - Clostridium beijerinckii ATCC 17795passes test
- Bacteroides fragilis ATCC 25285
passes test - Clostridium beijerinckii ATCC 17795passes test
Legal Information
ANAEROCULT is a trademark of Merck KGaA, Darmstadt, Germany
法规信息
监管及禁止进口产品
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Biochemical pharmacology, 56(7), 871-879 (1998-10-17)
While a differential sensitivity to cyclic AMP (cAMP)-mediated signaling between Th1 and Th2 cells has been hypothesized, differential activity of downstream signaling through cAMP-dependent protein kinase (cAK) isoforms remains unexplored. We herein report the effects of type 1- and type
H Yokozaki et al.
Cancer research, 52(9), 2504-2508 (1992-05-01)
A set of adenosine 3':5'-monophosphate (cAMP) analogues that combine exocyclic sulfur substitutions in the equatorial (Rp) or the axial (Sp) position of the cyclophosphate ring with modifications in the adenine base of cAMP were tested for their effect on the
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The Journal of biological chemistry, 270(35), 20599-20607 (1995-09-01)
Novel (Rp)-cAMPS analogs differed widely in ability to antagonize cAMP activation of pure cAMP-dependent protein kinase I and II and to antagonize actions of cAMP on gene expression, shape change, apoptosis, DNA replication, and protein phosphorylation in intact cells. These
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