855810P
Avanti
26:0 溶血 PC
Avanti Research™ - A Croda Brand
别名:
1-十六烷酰基-sn-甘油-3-磷酸胆碱；PC(26:0/0:0)
Product Name
26:0 溶血 PC, 1-hexacosanoyl-2-hydroxy-sn-glycero-3-phosphocholine, powder
方案
>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)
表单
powder
包装
pkg of 1 × 10 mg (855810P-10mg)
pkg of 1 × 25 mg (855810P-25mg)
pkg of 1 × 5 mg (855810P-5mg)
制造商/商品名称
Avanti Research™ - A Croda Brand 855810P
运输
dry ice
储存温度
−20°C
一般描述
溶血磷脂酰胆碱（LPC）是一种具有生物活性的促炎脂质，其极性头部含有胆碱基团。它是由病理反应产生的。
应用
26:0 Lyso PC可用作提取C26:0-溶血磷脂酰胆碱（LPC）的内标。
生化/生理作用
溶血磷脂酰胆碱（LPC）诱导许多第二信使，包括蛋白激酶C、细胞外信号调节激酶和蛋白酪氨酸激酶。它可改变不同类型细胞的各种生物学功能，包括内皮细胞、平滑肌细胞、单核细胞、巨噬细胞和T细胞。LPC与动脉粥样硬化和炎性疾病有关。
包装
5 mL棕色玻璃螺旋盖样品瓶（855810P-10mg）
5 mL棕色玻璃螺旋盖样品瓶（855810P-25mg）
5 mL棕色玻璃螺旋盖样品瓶（855810P-5mg）
法律信息
Avanti Research is a trademark of Avanti Polar Lipids, LLC
储存分类代码
11 - Combustible Solids
Xinying Hong et al.
Genetics in medicine : official journal of the American College of Medical Genetics (2020-04-21)
To develop a multiplexed assay for the newborn screening of lysosomal storage disorders and additional inborn errors in a flexible, comprehensive, and affordable manner to keep up with the expansion of the newborn screening panel. Ultraperformance liquid chromatography-tandem mass spectrometry
A thyroid hormone-based strategy for correcting the biochemical abnormality in X-linked adrenoleukodystrophy
Hartley MD, et al.
Endocrinology, 158(5), 1328-1338 (2017)
Analysis of phospholipid species in rat peritoneal surface layer by liquid chromatography/electrospray ionization ion-trap mass spectrometry
Gao F, et al.
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1761(7), 667-676 (2006)
Kelsey B Law et al.
Autophagy, 13(5), 868-884 (2017-05-20)
Peroxisome biogenesis disorders (PBDs) are metabolic disorders caused by the loss of peroxisomes. The majority of PBDs result from mutation in one of 3 genes that encode for the peroxisomal AAA ATPase complex (AAA-complex) required for cycling PEX5 for peroxisomal
R E Stafford et al.
Biochemistry, 28(12), 5113-5120 (1989-06-13)
The critical micelle concentration (cmc) of several lysophospholipids and of a lysophospholipid analogue was determined from surface tension measurements using the maximum bubble pressure method and/or 31P NMR. The use of the maximum bubble pressure method has now been extended
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