ET0200
E-TOXATE™ Kit
sufficient for 20 assays
Synonym(s):
Endotoxin detection kit
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About This Item
UNSPSC Code:
12352202
NACRES:
NA.84
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General description
E-Toxate™ Kit prepared from Limulus polyphemus amebocyte lysate (LAL) is suitable for the detection and quantification of endotoxins for research purposes.
Application
E-Toxate™ Kit has been used to determine the endotoxins:
- from Tabebuia chrysantha and Tabebuia rosea plant methanolic extracts
- from human pentameric C-reactive protein (pCRP)
- in the Diptheria toxin preparations
The E-TOXATE Kit was used to determine the number of bacteria in suspensions of group B streptococci used to infect rats for models of sepsis.
Features and Benefits
- Highly sensitive to endotoxins
- Simple and rapid detection
- Cost-effective
Legal Information
E-Toxate is a trademark of Sigma-Aldrich Co. LLC
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Storage Class Code
12 - Non Combustible Liquids
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Priscila Raquel Martins et al.
Memorias do Instituto Oswaldo Cruz, 103(3), 244-250 (2008-06-12)
A polysaccharide-rich fraction (ATF) of medicinal mushroom Agaricus brasiliensis was evaluated on the candidacidal activity, H2O2 and nitric oxide (NO) production, and expression of mannose receptors by murine peritoneal macrophages. Mice received three intraperitoneal (i.p.) injections of ATF and after
Priscila Raquel Martins et al.
The journal of venomous animals and toxins including tropical diseases, 23, 17-17 (2017-03-28)
Agaricus brasiliensis is a medicinal mushroom with immunomodulatory and antitumor activities attributed to the β-glucans presented in the polysaccharide fraction of its fruiting body. Since β-glucans enhance cellular immunoresponsiveness, in this study we aimed to evaluate the effect of an
G Teti et al.
Infection and immunity, 61(1), 227-235 (1993-01-01)
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Molecular therapy : the journal of the American Society of Gene Therapy, 14(4), 588-598 (2006-05-31)
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Polyelectrolyte nanoparticle constructs (NPs) comprising salmon calcitonin (sCT), chitosan (CS), and hyaluronic acid (HA) were previously established as having anti-inflammatory potential when injected via the intra-articular (i.a.) route to a mouse model. We attempted to translate the formulation to a
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