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重要文件

810130P

Avanti

16:0-06:0 NBD PC

Avanti Research - A Croda Brand 810130P, powder

同義詞:

1-棕榈酰基-2-{6-[(7-硝基-2-1,3-苯并恶二唑-4-基)氨基]己酰基}-sn-甘油基-3-磷酸胆碱

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About This Item

經驗公式(希爾表示法):
C36H62N5O11P
CAS號碼:
分子量::
771.88
MDL號碼:
分類程式碼代碼:
12352211
NACRES:
NA.25

化驗

>99% (TLC)

形狀

powder

包裝

pkg of 1 × 1 mg (810130P-1mg)
pkg of 5 × 1 mg (810130P-5mg)

製造商/商標名

Avanti Research - A Croda Brand 810130P

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

16:0-06:0 NBD PC(1-棕榈酰基-2-{6-[(7-硝基-2-1,3-苯并恶二唑-4-基)氨基]己酰基}-sn-甘油-3-磷酸胆碱)是磷脂酰胆碱的荧光类似物。

應用

16:0-06:0 NBD PC(1-棕榈酰基-2-{6-[(7-硝基-2-1,3-苯并恶二唑-4-基)氨基]己酰基}-sn-甘油-3-磷酸胆碱)已用于NBD-磷脂易位测定。它可以用作分子荧光标记物,以在摩擦试验期间标记脂质,用作酶底物特异性测定的底物以及制备小的单层脂质体。

生化/生理作用

16:0-06:0 NBD PC(1-棕榈酰基-2-{6-[(7-硝基-2-1,3-苯并恶二唑-4-基)氨基]己酰基}-sn-甘油-3-磷酸胆碱)充当潜在的荧光探针。它用于定量可溶性和膜结合磷脂酶A2(PLA2)的活性。7-硝基苯-2-氧杂-1,3-二氮杂-4-基(NBD)衍生物被广泛用作生物膜和模型膜中天然脂质的荧光类似物,以研究各种过程。

包裝

5 mL琥珀色玻璃螺旋盖小瓶(810130P-1mg)
5 mL琥珀色玻璃螺旋盖小瓶(810130P-5mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids


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分析證明 (COA)

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Effects of fluorescent probe NBD-PC on the structure, dynamics and phase transition of DPPC. A molecular dynamics and differential scanning calorimetry study
Loura L, et al.
Biochimica et Biophysica Acta - Biomembranes, 1778(2), 491-501 (2008)
In vitro analysis of the Staphylococcus aureus lipoteichoic acid synthase enzyme using fluorescently labeled lipids
Karatsa-Dodgson MW, et al.
Journal of Bacteriology, 192(20), 5341-5349 (2010)
The use of C6-NBD-PC for assaying phospholipase A2-activity: scope and limitations
Meyuhas D, et al.
Biochimica et Biophysica Acta, Lipids and Lipid Metabolism, 1124(3), 223-232 (1992)
Role of the biomolecular interactions in the structure and tribological properties of synovial fluid
Mirea DA, et al.
Tribology International, 59(3), 302-311 (2013)
Lenka Grycova et al.
PloS one, 7(10), e48437-e48437 (2012-11-03)
TRPV1 is a nonselective cation channel that integrates wide range of painful stimuli. It has been shown that its activity could be modulated by intracellular ligands PIP2 or calmodulin (CaM). The detailed localization and description of PIP2 interaction sites remain

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