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Documentos

855779P

Avanti

22:0 Lyso PC

1-behenoyl-2-hydroxy-sn-glycero-3-phosphocholine, powder

Sinónimos:

1-docosanoyl-sn-glycero-3-phosphocholine; PC(22:0/0:0)

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About This Item

Fórmula empírica (notación de Hill):
C30H62NO7P
Número de CAS:
125146-65-8
Peso molecular:
579.79
UNSPSC Code:
51191904
NACRES:
NA.25

assay

>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)

form

powder

packaging

pkg of 1 × 25 mg (855779P-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 855779P

shipped in

dry ice

storage temp.

−20°C

SMILES string

O[C@](COP([O-])(OCC[N+](C)(C)C)=O)([H])COC(CCCCCCCCCCCCCCCCCCCCC)=O

Categorías relacionadas

Application

22:0 Lyso PC may be used as a standard to screen X-linked adrenoleukodystrophy (X-ALD) in newborns using positive ion electrospray (ESI) combined liquid chromatography-tandem spectrometric (LC-MS/MS) technique.

Packaging

5 mL Amber Glass Screw Cap Vial (855779P-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

also commonly purchased with this product

Referencia del producto
Descripción
Precios

Storage Class

11 - Combustible Solids

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) method
Hubbard WC, et al.
Molecular Genetics and Metabolism, 97(3), 212-220 (2009)
Walter C Hubbard et al.
Molecular genetics and metabolism, 89(1-2), 185-187 (2006-07-11)
Utilizing combined liquid chromatography-tandem mass spectrometry (LC-MS/MS) as the analytical method, we have demonstrated a ten to sixtyfold excess of lysophosphatidyl choline containing hexacosanoic acid (26:0) in dried blood spots on a filter paper matrix from 25 male patients with
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
Francesca Saitta et al.
Colloids and surfaces. B, Biointerfaces, 186, 110715-110715 (2019-12-17)
A fifteen-components model membrane that reflected the 80 % of phospholipids present in Insulin Secretory Granules was obtained and thermodynamic exploitation was performed, through micro-DSC, in order to assess the synergic contributions to the stability of a mixed complex system

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