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Merck
CN

L6386

脂多糖 来源于伤寒沙门氏菌

purified by phenol extraction

别名:

LPS

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关于此项目

UNSPSC Code:
12352201
NACRES:
NA.25
MDL number:
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产品名称

脂多糖 来源于伤寒沙门氏菌, purified by phenol extraction

biological source

bacterial (Salmonella typhosa)

form

lyophilized powder

purified by

phenol extraction

impurities

<3% Protein (Lowry)

color

white to yellow cast

solubility

water: 4.90-5.10 mg/mL, faintly hazy to hazy, colorless to faintly yellow

shipped in

ambient

storage temp.

2-8°C

Quality Level

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Application

脂多糖(LPS)是革兰氏阴性细菌细胞壁的特征成分。LPS 及其脂质 A 部分通过 Toll 样受体 4(TLR4)刺激先天免疫系统的细胞,TLR4 是 Toll 样受体蛋白家族的成员,它能识别常见的病原体相关分子模式(PAMP)。

Biochem/physiol Actions

脂多糖(LPS)位于膜的外层,并且在非包封的菌株中暴露在细胞表面上。它们有助于外膜的完整性,并保护细胞免受胆汁盐和亲脂性抗生素的作用。

General description

本产品是从伤寒沙门氏菌中提取的苯酚。来源菌株为 ATCC 10749。

Other Notes

为了全面了解我们针对客户研究提供的各种脂多糖产品,建议您访问我们的碳水化合物分类页面。

Preparation Note

产物可溶于水(5mg/ml)或细胞培养基(1mg/ml),产生浑浊的淡黄色溶液。在经过涡旋,并升温至 70-80oC 后,含水盐水变得更浓缩,但仍然浑浊(20mg/ml)。脂多糖分子在每种溶剂中均形成胶束。在水和磷酸盐缓冲盐水中观察到浑浊的溶液。使用有机溶剂,溶液也是浑浊的。甲醇产生具有漂浮物的浑浊悬浮液,而水则产生均匀浑浊的溶液。

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 2 Oral

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yingjian Liang et al.
European journal of pharmacology, 833, 432-440 (2018-07-08)
Immune cell death caused by neutrophil extracellular traps (NETs), referred to as NETosis, can contribute to the pathogenesis of endotoxemia and organ damage. Although the mechanisms by which infection induces NETosis and how that leads to organ dysfunction remain largely
Yongqing Li et al.
Surgery, 150(3), 442-451 (2011-09-01)
Circulating proteins may serve as biomarkers for the early diagnosis and treatment of shock. We have recently demonstrated that treatment with suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, significantly improves survival in a rodent model of lipopolysaccharide (LPS)-induced septic
Céline Tellier et al.
Neoplasia (New York, N.Y.), 17(1), 66-78 (2015-01-28)
Abnormal architecture of the tumor blood network, as well as heterogeneous erythrocyte flow, leads to temporal fluctuations in tissue oxygen tension exposing tumor and stromal cells to cycling hypoxia. Inflammation is another feature of tumor microenvironment and is considered as
Amy G Clark et al.
Autoimmunity, 46(3), 188-204 (2012-11-20)
Autoantibodies to diverse antigens escape regulation in systemic lupus erythematosus under the influence of a multitude of predisposing genes. To gain insight into the differential impact of diverse genetic backgrounds on tolerance mechanisms controlling autoantibody production in lupus, we established
Sebastian Steven et al.
British journal of pharmacology, 174(12), 1620-1632 (2016-07-21)
Excessive inflammation in sepsis causes microvascular thrombosis and thrombocytopenia associated with organ dysfunction and high mortality. The present studies aimed to investigate whether inhibition of dipeptidyl peptidase-4 (DPP-4) and supplementation with glucagon-like peptide-1 (GLP-1) receptor agonists improved endotoxaemia-associated microvascular thrombosis

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