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810195C

Avanti

18:1-12:0 NBD PS

Avanti Research - A Croda Brand 810195C

Synonym(s):

1-oleoyl-2-{12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl}-sn-glycero-3-phosphoserine (ammonium salt)

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About This Item

Empirical Formula (Hill Notation):
C42H73N6O13P
CAS Number:
Molecular Weight:
901.04
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 1 mL (810195C-1mg)

manufacturer/tradename

Avanti Research - A Croda Brand 810195C

concentration

1 mg/mL (810195C-1mg)

shipped in

dry ice

storage temp.

−20°C

General description

Phosphatidylserine (PS) is a minor membrane phospholipid. This anionic phospholipid contains a polar head group and two long hydrophobic acyl chains. 1 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) PS is a fluorescent probe containing NBD at the headgroup of PS.

Application

18:1-12:0 NBD PS or 1-oleoyl-2-{12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl}-sn-glycero-3-phosphoserine (ammonium salt) has been used in donor liposomes to determine the phospholipid transfer activity of the synaptic vesicle membrane protein, VAT-1 and phosphatidic acid (PA) transfer by Ups1−Mdm35 system in mitochondria. 18:1-12:0 NBD PS is also suitable for the determination of in vitro phosphatidylserine decarboxylase (Psd1) activity.

Packaging

5 mL Amber Glass Screw Cap Vial (810195C-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictograms

Skull and crossbonesHealth hazard

Signal Word

Danger

Hazard Classifications

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

Target Organs

Central nervous system, Liver,Kidney

WGK

WGK 3


Certificates of Analysis (COA)

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Structural and mechanistic insights into phospholipid transfer by Ups1?Mdm35 in mitochondria
Yasunori W, et al.
Nature Communications null
The distribution and function of phosphatidylserine in cellular membranes
Leventis PA and Grinstein S
Annual Review of Biophysics null
Phosphatidylserine and the human brain
Glade MJ and Smith K
Nutrition null
Structural Basis for Phosphatidylethanolamine Biosynthesis by Bacterial Phosphatidylserine Decarboxylase
Yasunori W, et al.
Structure null
Organization and dynamics of N-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)-labeled lipids: a fluorescence approach
Mukherjee S, et al.
Chemistry and Physics of Lipids null

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