1,2-dioleoyl-sn-glycero-3-phospho-(1'-myoinositol-3',4'-bisphosphate)(ammonium salt)

≥99%

Reagent Code: #180295
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CAS Number 799268-54-5

science Other reagents with same CAS 799268-54-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1074.16 g/mol
Formula C₄₅H₉₄N₃O₁₉P₃
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used in lipid signaling research to study phosphoinositide-dependent cellular processes. Serves as a synthetic analog of PI(3,4)P2, a key lipid second messenger involved in regulating membrane trafficking, cell survival, and insulin signaling. Employed in in vitro assays to investigate the activity and specificity of phosphoinositide-binding domains, such as PH, PX, and FYVE domains. Also utilized in liposome formulations to mimic physiological membranes and study protein-lipid interactions. Its defined acyl chain composition (di-oleoyl) ensures consistent biophysical properties in membrane studies.

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Size Availability Unit Price Quantity
inventory 100μg
10-20 days ฿10,800.00
inventory 500μg
10-20 days ฿47,000.00

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1,2-dioleoyl-sn-glycero-3-phospho-(1'-myoinositol-3',4'-bisphosphate)(ammonium salt)
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Used in lipid signaling research to study phosphoinositide-dependent cellular processes. Serves as a synthetic analog of PI(3,4)P2, a key lipid second messenger involved in regulating membrane trafficking, cell survival, and insulin signaling. Employed in in vitro assays to investigate the activity and specificity of phosphoinositide-binding domains, such as PH, PX, and FYVE domains. Also utilized in liposome formulations to mimic physiological membranes and study protein-lipid interactions. Its defined

Used in lipid signaling research to study phosphoinositide-dependent cellular processes. Serves as a synthetic analog of PI(3,4)P2, a key lipid second messenger involved in regulating membrane trafficking, cell survival, and insulin signaling. Employed in in vitro assays to investigate the activity and specificity of phosphoinositide-binding domains, such as PH, PX, and FYVE domains. Also utilized in liposome formulations to mimic physiological membranes and study protein-lipid interactions. Its defined acyl chain composition (di-oleoyl) ensures consistent biophysical properties in membrane studies.

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