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Key Documents

850185P

Avanti

08:0 PI (4,5) P2

Avanti Research - A Croda Brand

同義詞:

PIP2[4′,5′](8:0/8:0); 110665

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About This Item

經驗公式(希爾表示法):
C25H58N3O19P3
CAS號碼:
分子量::
797.66
分類程式碼代碼:
51191904
NACRES:
NA.25

描述

1,2-dioctanoyl-sn-glycero-3-phospho-(1′-myo-inositol-4′,5′-bisphosphate) (ammonium salt)

化驗

>99% (TLC)

形狀

powder

包裝

pkg of 1 × 100 μg (with stopper and crimp cap (850185P-100ug))
pkg of 1 × 500 μg (with stopper and crimp cap (850185P-500ug))

製造商/商標名

Avanti Research - A Croda Brand

脂質類型

cardiolipins
phospholipids

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](OP(O)([O-])=O)[C@H](OP([O-])(O)=O)[C@@H](O)[C@H]1O)=O)(OC(CCCCCCC)=O)COC(CCCCCCC)=O.[NH4+].[NH4+].[NH4+]

一般說明

尽管PI(4,5)P2是细胞膜的次要成分,但它作为许多重要信号转导蛋白的底物发挥着重要作用。PI(4,5)P2是IP3/DAG途径中的中间体,在该途径中,它被磷脂酶C水解,释放第二信使,即肌醇1,4,5-三磷酸(IP3)和二酰基甘油(DAG)。PI(4,5)P2也是PI 3-激酶的底物,可被磷酸化为PI(3,4,5)P3,后者是下游信号转导成分(如蛋白激酶AKT)的激活剂。PI(4,5)P2的二辛酰基衍生物比其长链对应物更易溶于水。

應用

08:0 PI(4,5)P2适用于识别瞬时受体电位香草酸4(TRPV4 N)末端的结合位点。它可用于体外结合试验,以测定G蛋白偶联受体激酶(GRK)和β2肾上腺素能受体(β2AR)的结合。

包裝

带塞子和压接盖的2 mL棕色血清瓶(850185P-100ug)
带塞子和压接盖的2 mL棕色血清瓶(850185P-500ug)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids


分析證明 (COA)

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存取文件庫

Scott B Hansen et al.
Nature, 477(7365), 495-498 (2011-08-30)
The regulation of ion channel activity by specific lipid molecules is widely recognized as an integral component of electrical signalling in cells. In particular, phosphatidylinositol 4,5-bisphosphate (PIP(2)), a minor yet dynamic phospholipid component of cell membranes, is known to regulate
Structural Basis of TRPV4 N Terminus Interaction with Syndapin/PACSIN1-3 and PIP2
Goretzki B, et al.
Structure, 26(12), 1583-1593 (2018)
George Khelashvili et al.
Biochemistry, 51(39), 7685-7698 (2012-09-07)
Syntaxin (STX) is a N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) protein that binds to the plasma membrane and regulates ion channels and neurotransmitter transporters. Experiments have established the involvement of the N-terminal segment of STX in direct protein-protein interactions and
Tao Liang et al.
The Journal of biological chemistry, 289(9), 6028-6040 (2014-01-17)
In β-cells, syntaxin (Syn)-1A interacts with SUR1 to inhibit ATP-sensitive potassium channels (KATP channels). PIP2 binds the Kir6.2 subunit to open KATP channels. PIP2 also modifies Syn-1A clustering in plasma membrane (PM) that may alter Syn-1A actions on PM proteins
Structural and functional analysis of a beta2-adrenergic receptor complex with GRK5
Komolov KE, et al.
Cell, 169(3), 407-421 (2017)

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