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安全信息

LM6005

Avanti

Cer/Sph 混合物 II

Avanti Polar Lipids

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别名:
Cer/Sph 混合物 II, 神经酰胺/Sphingoid内标混合物II
UNSPSC代码:
41116107
NACRES:
NA.25

形式

ethanol solution

包装

pkg of 1 × 1 mL (LM6005-1EA)

制造商/商品名称

Avanti Polar Lipids

浓度

~10 μg/mL (Refer to C of A for lot specific concentration. )

应用

lipidomics
metabolomics

运输

dry ice

储存温度

−20°C

应用

Cer/Sph混合物II已用于:作为液相-电喷雾电离-串联质谱法 (LC ESI-MS/MS)进行鞘磷脂定量分析的内标混合物,用于通过液相色谱-质谱(LC-MS)分析法对仪器稳定性进行质量控制检查,作为甲基叔丁基醚(MTBE)/乙醇提取法从血清和组织样品中提取脂质的内标混合物。

包装

2mL棕色玻璃密封安瓿(LM6005-1EA)

象形图

FlameExclamation mark

警示用语:

Danger

危险声明

危险分类

Eye Irrit. 2 - Flam. Liq. 2

WGK

WGK 1

闪点(°F)

55.4 °F

闪点(°C)

13 °C

法规信息

危险化学品

分析证书(COA)

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Merja Joensuu et al.
Progress in neuro-psychopharmacology & biological psychiatry, 84(Pt B), 362-381 (2017-09-06)
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Diego Arango et al.
The American journal of pathology, 180(4), 1509-1521 (2012-02-22)
Colorectal cancers (CRCs) are classified as having microsatellite instability (MSI) or chromosomal instability (CIN); herein termed microsatellite stable (MSS). MSI colon cancers frequently display a poorly differentiated histology for which the molecular basis is not well understood. Gene expression and
Jeffrey Molendijk et al.
Biomolecules, 10(5) (2020-05-21)
Esophageal adenocarcinoma (EAC) incidence has been rapidly increasing, potentially associated with the prevalence of the risk factors gastroesophageal reflux disease (GERD), obesity, high-fat diet (HFD), and the precursor condition Barrett's esophagus (BE). EAC development occurs over several years, with stepwise
Seema Khurana et al.
FEBS letters, 582(14), 2128-2139 (2008-03-01)
Villin is a tissue-specific actin modifying protein that is associated with actin filaments in the microvilli and terminal web of epithelial cells. It belongs to a large family of actin-binding proteins which includes actin-capping, -nucleating and/or -severing proteins such as
Nitai C Hait et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(3), 4293-4310 (2020-02-06)
Sphingosine kinase 2 (SphK2) is known to phosphorylate the nuclear sphingolipid metabolite to generate sphingosine-1-phosphate (S1P). Nuclear S1P is involved in epigenetic regulation of gene expression; however, the underlying mechanisms are not well understood. In this work, we have identified

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