推荐产品
产品线
BioReagent
质量水平
方案
≥99.0% (UV)
表单
crystals
mp
>300 °C (lit.)
溶解性
ethanol: soluble
methanol: soluble
荧光
λex 498 nm; λem 520 nm in methanol
适用性
suitable for fluorescence
SMILES字符串
Cl.Nc1ccc2c(OC3=CC(=N)C=CC3=C2c4ccccc4C(O)=O)c1
InChI
1S/C20H14N2O3.ClH/c21-11-5-7-15-17(9-11)25-18-10-12(22)6-8-16(18)19(15)13-3-1-2-4-14(13)20(23)24;/h1-10,21H,22H2,(H,23,24);1H
InChI key
JNGRENQDBKMCCR-UHFFFAOYSA-N
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相关类别
一般描述
罗丹明110或R110是一种三苯甲烷染料,可发射出强烈的绿色荧光。能发出高强度荧光是由于存在作为给电子基团的氨基。罗丹明110的最大激发光谱和发射光谱分别为502.4/521.6521.6 nm。
应用
罗丹明110被用于测定具有准确的动力学参数的蛋白酶活性。它被用于测量诱导细胞凋亡的半胱天冬酶活性。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(8), 1667-1672 (2003-05-09)
A simple and sensitive fluorescence quenching method for the determination of trace nitrite has been developed. The method is based on the reaction of Rhodamine 110 with nitrite in acidic medium to form a new compound, which has much lower
Analytical chemistry, 84(5), 2380-2387 (2012-02-14)
By site directed mutagenesis, we have produced recombinant mutants of human and mouse prethrombin-2 which are able to convert themselves autocatalytically into α-thrombin. We also have created a new method to amplify the signal of bioanalytical assays based on the
Journal of the American Chemical Society, 132(18), 6306-6308 (2010-04-20)
Access to native protein structure depends on precise polypeptide folding and assembly pathways. Identifying folding missteps that may lead to the nearly 40 protein misfolding diseases could feature prominently in the development of intervention strategies. Accordingly, we have investigated the
Clinical chemistry, 58(8), 1252-1259 (2012-06-06)
The calibrated automated thrombogram (CAT) assay in plasma is a versatile tool to investigate patients with hypo- or hypercoagulable phenotypes. The objective was to make this method applicable for whole blood measurements. Thin-layer technology and the use of a rhodamine
Bioconjugate chemistry, 22(10), 1932-1938 (2011-09-13)
Commonly used fluorogenic substrate analogues for the detection of protease activity contain two enzyme-cleavable bonds conjugated to the fluorophore. Enzymatic cleavage follows a two-step reaction with a monoamide intermediate. This intermediate shows fluorescence at the same wavelength as the final
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