216699-36-4 Usage
Description
6-ROX, SE, also known as 6-Carboxy-X-rhodamine N-succinimidyl ester, is a fluorescent probe and a rhodamine X derivative. It is an amine-reactive fluorescent probe used for labeling oligonucleotides and preparing labeled primers for real-time PCR applications.
Uses
Used in Molecular Biology:
6-ROX, SE is used as an amine-reactive fluorescent probe for labeling oligonucleotides, which allows for the detection and analysis of specific DNA or RNA sequences in various molecular biology techniques.
Used in Real-Time PCR:
6-ROX, SE is used as a labeling agent for the preparation of labeled primers, which are essential for real-time PCR. This enables the monitoring of PCR amplification in real-time, providing accurate quantification of target nucleic acid sequences.
Used in Fluorescence Detection:
As a rhodamine X derivative, 6-ROX, SE is used in fluorescence detection methods due to its strong fluorescence properties. This makes it suitable for various applications, such as fluorescence microscopy, flow cytometry, and other fluorescence-based assays.
Check Digit Verification of cas no
The CAS Registry Mumber 216699-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,6,9 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 216699-36:
(8*2)+(7*1)+(6*6)+(5*6)+(4*9)+(3*9)+(2*3)+(1*6)=164
164 % 10 = 4
So 216699-36-4 is a valid CAS Registry Number.
216699-36-4Relevant articles and documents
Hydroxylated Fluorescent Dyes for Live-Cell Labeling: Synthesis, Spectra and Super-Resolution STED
Butkevich, Alexey N.,Belov, Vladimir N.,Kolmakov, Kirill,Sokolov, Viktor V.,Shojaei, Heydar,Sidenstein, Sven C.,Kamin, Dirk,Matthias, Jessica,Vlijm, Rifka,Engelhardt, Johann,Hell, Stefan W.
, p. 12114 - 12119 (2017/09/14)
Hydroxylated rhodamines, carbopyronines, silico- and germanorhodamines with absorption maxima in the range of 530–640 nm were prepared and applied in specific labeling of living cells. The direct and high-yielding entry to germa- and silaxanthones tolerates the presence of protected heteroatoms and may be considered for the syntheses of various sila- and germafluoresceins, as well as -rhodols. Application in stimulated emission depletion (STED) fluorescence microscopy revealed a resolution of 50–75 nm in one- and two-color imaging of vimentin-HaloTag fused protein and native tubulin. The established structure–property relationships allow for prediction of the spectral properties and the positions of spirolactone/zwitterion equilibria for the new analogues of rhodamines, carbo-, silico-, and germanorhodamines using simple additive schemes.