1,2-Diarachidoyl-sn-glycero-3-phosphatidylcholine
Modify Date: 2024-01-15 20:19:29
1,2-Diarachidoyl-sn-glycero-3-phosphatidylcholine structure
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Common Name | 1,2-Diarachidoyl-sn-glycero-3-phosphatidylcholine | ||
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| CAS Number | 61596-53-0 | Molecular Weight | 846.252 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C48H96NO8P | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Name | 1,2-Diarachidoyl-sn-glycero-3-phosphocholine |
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| Synonym | More Synonyms |
| Molecular Formula | C48H96NO8P |
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| Molecular Weight | 846.252 |
| Exact Mass | 845.687378 |
| PSA | 121.00000 |
| LogP | 15.13 |
| Storage condition | -20°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xn |
| RIDADR | NONH for all modes of transport |
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Lipidomic analyses of female mice lacking hepatic lipase and endothelial lipase indicate selective modulation of plasma lipid species.
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Relating toxicity to transfection: using sphingosine to maintain prolonged expression in vitro.
Mol. Pharm. 12(1) , 264-73, (2015) Cationic reagents are commonly used to facilitate DNA delivery, and transfection experiments are typically initiated in cell culture where the optimal charge ratio is determined. While transfection ra... |
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Evidence for segregation of sphingomyelin and cholesterol during formation of COPI-coated vesicles.
J. Cell Biol. 151 , 507-18, (2000) In higher eukaryotes, phospholipid and cholesterol synthesis occurs mainly in the endoplasmic reticulum, whereas sphingomyelin and higher glycosphingolipids are synthesized in the Golgi apparatus. Lip... |
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