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About This Item
經驗公式（希爾表示法）:
C20H13NO5
CAS號碼:
分子量：:
347.32
Beilstein:
51708
EC號碼:
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:
NACRES:
NA.47
推薦產品
形狀
powder
品質等級
mp
285 °C (dec.) (lit.)
溶解度
methanol: 1 mg/mL, clear, yellow to very dark yellow-orange
λmax
495 nm
應用
diagnostic assay manufacturing
hematology
histology
儲存溫度
room temp
SMILES 字串
Nc1ccc2C(=O)OC3(c4ccc(O)cc4Oc5cc(O)ccc35)c2c1
InChI
1S/C20H13NO5/c21-10-1-4-13-16(7-10)20(26-19(13)24)14-5-2-11(22)8-17(14)25-18-9-12(23)3-6-15(18)20/h1-9,22-23H,21H2
InChI 密鑰
YOAWSYSKQHLFPM-UHFFFAOYSA-N
尋找類似的產品？ 前往 產品比較指南
應用
6-氨基荧光素已被用于确定其增强聚r（A-U）的抗病毒活性的能力。
6-氨基荧光素已被证明是基于富勒烯的脂质体纳米结构（称为'buckysomes'）的有效荧光标记试剂。溶解在0.1N NaOH中的6-氨基荧光素可通过490nm处的最大吸光度进行定量。溶解在6N HCl中的脱羧化的6-氨基荧光素（通过在110℃恒沸24小时制备）可通过454nm处的最大吸光度进行定量。醛基是通过对蛋白质的氧化损伤形成的，其可以通过与脱羧的6-氨基荧光素结合来检测。
其他說明
注意：不要与荧光胺混淆。
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
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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’.。
Self assembly of amphiphilic C60 fullerene derivatives into nanoscale supramolecular structures
Partha R
Journal of Nanobiotechnology (2007)
I Climent et al.
Analytical biochemistry, 182(2), 226-232 (1989-11-01)
Oxidative modification of proteins is implicated in a number of physiologic and pathologic processes. Metal-catalyzed oxidative modification usually causes inactivation of enzymes and the appearance of carbonyl groups in amino acid side chains of the protein. We describe use of
W.E.G. Muller and H.C. Schroder
Biological Response Modifiers ? Interferons, Double-Stranded RNA and 2?,5?-Oligoadenylates (2012)
K C Ingham et al.
Biochimica et biophysica acta, 670(2), 181-189 (1981-09-29)
A method for covalent attachment of a fluorescent molecule to the carbohydrate moieties of glycoproteins is described. The glycoproteins were oxidized with periodate under mild conditions selective for sialic acid (Van Lenten, L. and Ashwell, G. (1971) J. Biol. Chem.
Miju Kim et al.
ACS nano, 9(8), 8269-8278 (2015-07-15)
Polyelectrolyte microcapsules represent versatile stimuli-responsive structures that enable the encapsulation, protection, and release of active agents. Their conventional preparation methods, however, tend to be time-consuming, yield low encapsulation efficiency, and seldom allow for the dual incorporation of hydrophilic and hydrophobic
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