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Merck

ET0100

E-Toxate Kit

sufficient for 50 assays

Sinónimos:

Endotoxin detection kit

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NACRES:
NA.83
UNSPSC Code:
12352202
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usage

sufficient for 50 assays

Quality Level

storage temp.

2-8°C

General description

E-Toxate Kit made from Limulus polyphemus amebocyte lysate (LAL) is developed for the detection and semi-quantitation of endotoxins.

Application

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.
E-Toxate Kit has been used for endotoxin detection:
  • in chitosan and collagen solutions
  • in C-reactive protein (CRP) samples
  • in the ethanolic plant extracts from Tinospora cordifolia

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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Los componentes del kit también están disponibles por separado

Referencia del producto
Descripción
SDS & Precios

  • E-Toxate Endotoxin standard, for endotoxin quantitation 1 mL/vial
    SDS

  • E-Toxate reagent from Limulus polyphemus, sufficient for 50 tests 1 mL/vial
    SDS

  • E-Toxate Water, endotoxin, free 30 mL
    SDS

wgk

WGK 3

Clase de almacenamiento

12 - Non Combustible Liquids



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Nicola R Sproston et al.
Frontiers in immunology, 9, 1500-1500 (2018-07-18)
Inflammation is regulated by many endogenous factors including estrogen, a steroid hormone that declines with increasing age, leading to excessive inflammation in the elderly. C-reactive protein (CRP) is an acute phase inflammatory protein that exists in two forms, native CRP
Ju-Suk Nam et al.
Journal of biomedical materials research. Part A, 105(3), 912-926 (2017-01-12)
Periprosthetic osteolysis remains the leading obstacle for total joint replacements. Primarily, it was thought that aseptic loosening is mainly caused by macrophage mediated inflammatory process arising from production of wear debris. The role of osteoclasts and its sequential bone resorption
Mathias Gehrmann et al.
PloS one, 7(7), e41341-e41341 (2012-07-26)
We have previously reported that human recombinant granzyme B (grB) mediates apoptosis in membrane heat shock protein 70 (Hsp70)-positive tumor cells in a perforin-independent manner. Optical imaging of uptake kinetics revealed co-localization of grB with recycling endosomes (Rab9/11) as early



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SKUGTIN
ET0100-1KT04061826738528