推荐产品
化驗
>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)
形狀
liquid
包裝
pkg of 1 × 2.5 mL (855676C-25mg)
pkg of 2 × 4 mL (855676C-200mg)
製造商／商標名
Avanti Research™ - A Croda Brand 855676C
濃度
10 mg/mL (855676C-25mg)
25 mg/mL (855676C-200mg)
運輸包裝
dry ice
儲存溫度
−20°C
InChI
1S/C25H52NO7P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-25(28)31-22-24(27)23-33-34(29,30)32-21-20-26(2,3)4/h24,27H,5-23H2,1-4H3/t24-/m1/s1
InChI 密鑰
SRRQPVVYXBTRQK-XMMPIXPASA-N
應用
17:0 Lyso PC has been used for the extraction of lipids from the blood samples.
包裝
5 mL Clear Glass Sealed Ampule (855676C-200mg)
5 mL Clear Glass Sealed Ampule (855676C-25mg)
法律資訊
Avanti Research is a trademark of Avanti Polar Lipids, LLC
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3
標靶器官
Central nervous system, Liver,Kidney
水污染物質分類（WGK）
WGK 3
Generation and quality control of lipidomics data for the alzheimer?s disease neuroimaging initiative cohort
Barupal DK, et al.
Scientific data, 5, 180263-180263 (2018)
Melania Gaggini et al.
International journal of molecular sciences, 20(24) (2020-01-01)
Metabolomics/lipidomics are important tools to identify novel biomarkers associated with liver damage. Patients with chronic liver disease (CLD) and hepatitis C virus (HCV) infection often have alterations in glucose, lipid and protein metabolism. The aim of this study was to
David B Iaea et al.
Biochimica et biophysica acta. Molecular and cell biology of lipids, 1865(4), 158609-158609 (2020-01-10)
STARD4, a member of the evolutionarily conserved START gene family, is a soluble sterol transport protein implicated in cholesterol sensing and maintenance of cellular homeostasis. STARD4 is widely expressed and has been shown to transfer sterol between liposomes as well
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
Jordon M Inloes et al.
Biochemistry, 57(39), 5759-5767 (2018-09-18)
Deleterious mutations in the serine hydrolase DDHD domain containing 1 (DDHD1) cause the SPG28 subtype of the neurological disease hereditary spastic paraplegia (HSP), which is characterized by axonal neuropathy and gait impairments. DDHD1 has been shown to display PLA1-type phospholipase
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