推薦產品
化驗
≥95% (HPLC)
形狀
lyophilized
分子量
calculated mol wt 501.66
包裝
pkg of 1 mg
製造商/商標名
Millipore
儲存條件
desiccated
protect from light
技術
cell based assay: suitable
顏色
off-white
螢光
λex 540 nm; λem 590 nm
檢測方法
fluorometric
運輸包裝
ambient
儲存溫度
−20°C
一般說明
Cyclooxygenase (COX), also known as Prostaglandin-endoperoxide synthase (PTGS), is the key enzyme in prostaglandin biosynthesis. There are two isozymes of cyclooxygenase: a constitutive COX-1 and an inducible COX-2, which differ in their regulation of expression and tissue distribution. COX-2 overexpression is prominent in inflammatory diseases, neurodegenerative disorders, and cancer. Directly monitoring COX-2 activity within its native environment poses an exciting approach to investigate the effect of the local environments on protein activity.
BioTracker CoxFluor Live Cell Dye is an isoform selective activity-based sensor for COX-2. The probe may be used for COX-2 inhibitor screening assays and for monitoring COX-2 activity in live cells by confocal microscopy or flow cytometry. CoxFluor strategically links a natural substrate with a dye precursor to engage both the cyclooxygenase and peroxidase activities of COX-2. This catalyzes the release of resorufin and the natural product, as supported by molecular dynamics and ensemble docking. CoxFluor enabled the detection of oxygen dependent changes in COX-2 activity that are independent of protein expression within live macrophage cells.
Spectral Properties
Absorbance: 540 nm
Emission: 590 nm
Reference:
1. Yadav, A. K., Reinhardt, C. J., Arango, A. S., Huff, H. C., Dong, L., Malkowski, M. G., ... & Chan, J. (2020). An Activity?Based Sensing Approach for the Detection of Cyclooxygenase?2 in Live Cells. Angewandte Chemie, 132(8), 3333-3340.
BioTracker CoxFluor Live Cell Dye is an isoform selective activity-based sensor for COX-2. The probe may be used for COX-2 inhibitor screening assays and for monitoring COX-2 activity in live cells by confocal microscopy or flow cytometry. CoxFluor strategically links a natural substrate with a dye precursor to engage both the cyclooxygenase and peroxidase activities of COX-2. This catalyzes the release of resorufin and the natural product, as supported by molecular dynamics and ensemble docking. CoxFluor enabled the detection of oxygen dependent changes in COX-2 activity that are independent of protein expression within live macrophage cells.
Spectral Properties
Absorbance: 540 nm
Emission: 590 nm
Reference:
1. Yadav, A. K., Reinhardt, C. J., Arango, A. S., Huff, H. C., Dong, L., Malkowski, M. G., ... & Chan, J. (2020). An Activity?Based Sensing Approach for the Detection of Cyclooxygenase?2 in Live Cells. Angewandte Chemie, 132(8), 3333-3340.
應用
Purity ≥ 95% confirmed by HPLC. Identification confirmed by HNMR, LC-MS, and elemental analysis.
特點和優勢
Fluorescent probe for monitoring COX-2 activity in live cells by confocal microscopy or flow cytometry.
外觀
Lyophilized. Off-white solid.
儲存和穩定性
Store at -20°C, desiccate and protect from light
Note: Centrifuge vial briefly to collect contents at bottom of vial before opening
Note: Centrifuge vial briefly to collect contents at bottom of vial before opening
其他說明
Live cell fluorescent imaging
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
Angewandte Chemie (International ed. in English), 59(8), 3307-3314 (2019-12-20)
Cyclooxygenase-2 (COX-2) overexpression is prominent in inflammatory diseases, neurodegenerative disorders, and cancer. Directly monitoring COX-2 activity within its native environment poses an exciting approach to account for and illuminate the effect of the local environments on protein activity. Herein, we
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