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品質水準
アッセイ
≥95%
フォーム
powder or crystals
反応適合性
reaction type: click chemistry
保管温度
−20°C
SMILES記法
O=CNCCOCCOCCOCCOCC#C.CN(C)C1=CC=C(C(C2=C(C([O-])=O)C=CC=C2)=C(C=C3)C(O4)=CC3=[N+](C)C)C4=C1
InChI Key
ZFKUPSPWMXEEIG-UHFFFAOYSA-N
関連するカテゴリー
アプリケーション
TAMRA alkyne is a red-fluorescent probe that through the alkyne group can be reacted with azides via a copper-catalyzed click reaction (CuAAC). TAMRA (tetramethylrhodamine) is a bright fluorescent probe and is compatible with various excitation sources including mercury arc, tungsten and xenon arc lamps, the 544 nm line of the Helium-Neon laser and the 532 nm green laser line.[1]{37[2]
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
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Selective imaging of Gram-negative and Gram-positive microbiotas in the mouse gut.
Wang W, et al.
Biochemistry, 56(30), 3889-3893 (2017)
Chemoselective modification of viral surfaces via bioorthogonal click chemistry.
Rubino F A, et al.
Journal of Visualized Experiments, 66 (2012)
Jacob Gubbens et al.
Chemistry & biology, 16(1), 3-14 (2009-01-28)
New lipid analogs mimicking the abundant membrane phospholipid phosphatidylcholine were developed to photocrosslink proteins interacting with phospholipid headgroups at the membrane interface. In addition to either a phenylazide or benzophenone photoactivatable moiety attached to the headgroup, the lipid analogs contained
アクティブなフィルタ
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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