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ET0300

Sigma-Aldrich

E-TOXATE™ Kit

sufficient for 100 assays

Sinónimos:

Endotoxin detection kit

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.84

usage

sufficient for 100 assays

Quality Level

200

storage temp.

−20°C

Application

E-TOXATE™ Kit has been used in the semiquantitative determination of endotoxin levels in 0.1 % (w/v) dispersions of polyelectrolyte nanoparticle construct (NPs) and 0.1 % (w/v) polymer solutions.

Legal Information

E-Toxate is a trademark of Sigma-Aldrich Co. LLC

Los componentes del kit también están disponibles por separado

Referencia del producto
Descripción
SDS
  • E8029E-Toxate™ Endotoxin standard, for endotoxin quantitation 1 mL/vialSDS
  • E8779E-Toxate™ reagent from Limulus polyphemus, sufficient for 20 tests 5 vial(s)SDS
  • 2107E-Toxate™ Water, endotoxin, free 5 x 30SDS

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ET0100

E-Toxate™ Kit, sufficient for 50 assays

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Storage Class

10 - Combustible liquids

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Intra-articular delivery of a nanocomplex comprising salmon calcitonin, hyaluronic acid, and chitosan using an equine model of joint inflammation.
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H E Çolakoğlu et al.
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The aim of this study was to investigate some of the growth and transcriptional factors originating from oocytes and granulosa cells in follicular fluid and to identify the relationships between the basic blood metabolite-metabolic hormones and intrafollicular lipopolysaccharide (LPS) concentrations.
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The development and maintenance of memory B cells (MBC) is dependent on germinal centres (GC) with follicular dendritic cell (FDC) networks. We have previously shown that FDC networks within GC of the spleen express a novel ligand for CD38 and
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Drug delivery and translational research, 8(5), 1421-1435 (2018-06-28)
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
Atsuko Hayashida et al.
The American journal of pathology, 174(2), 509-518 (2009-01-17)
In pneumonia caused by the bacterium Staphylococcus aureus, the intense inflammatory response that is triggered by this infection can lead to the development of lung injury. Little is known, however, about the impact of specific virulence factors on this inflammatory
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