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Nuclear Red™ DCS1 *5 mM DMSO Solution*

Fluorescence image of HeLa cells fixed with 4% formaldehyde then stained with iFluor 488 Phalloidin (Cat#23115, Green) and nuclei stain Nuclear Red™ DCS1 (Cat#17552, Red)
Fluorescence image of HeLa cells fixed with 4% formaldehyde then stained with iFluor 488 Phalloidin (Cat#23115, Green) and nuclei stain Nuclear Red™ DCS1 (Cat#17552, Red)
Fluorescence image of HeLa cells fixed with 4% formaldehyde then stained with iFluor 488 Phalloidin (Cat#23115, Green) and nuclei stain Nuclear Red™ DCS1 (Cat#17552, Red)
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Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
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Physical properties
Molecular weight671.42
SolventDMSO
Spectral properties
Excitation (nm)631
Emission (nm)651
Storage, safety and handling
Certificate of OriginDownload PDF
H-phraseH303, H313, H340
Hazard symbolT
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R68
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC41116134

OverviewpdfSDSpdfProtocol


Molecular weight
671.42
Excitation (nm)
631
Emission (nm)
651
Our Nuclear Red™ DCS1 is a fluorogenic, DNA-selective and cell-impermeant dye for analyzing DNA content in dead, fixed or apoptotic cells. The Nuclear Red™ DCS1 has its red fluorescence significantly enhanced upon binding to DNA. It can be used in fluorescence imaging, microplate and flow cytometry applications. This DNA-binding dye might be used for multicolor analysis of dead, fixed or apoptotic cells with proper filter sets.

Platform


Fluorescence microscope

ExcitationCy5 Filter
EmissionCy5 Filter
Recommended plateBlack wall/clear bottom

Example protocol


AT A GLANCE

Spectral Properties

Ex/Em = 631/651 nm (bound to DNA) 

SAMPLE EXPERIMENTAL PROTOCOL

Caution: The following protocol can be adapted for most cell types. Growth medium, cell density, the presence of other cell types, and factors may influence staining. Residual detergent on glassware may also affect the staining of many organisms and cause brightly stained material to appear in solutions with or without cells present.

  1. Add Nuclear Red™ DCS1 (2 to10 µM) into the fixed, dead or apoptotic cells (either suspension or adherent) and incubate the cells for 15 to 60 minutes.

    Note: In initial experiments, it is advisable to test a wide range of dye concentrations in order to determine the optimal concentration that yields the desired result.

    Optional: Wash the cells twice with Hanks and 20 mM HEPES buffer (HBSS) or a buffer of your choice. Then fill the wells with fresh HBSS or growth medium.

  2. Observe the cells using a fluorescence microscope, fluorescence microplate reader, or flow cytometer equipped with the desired filter set. 

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Nuclear Red™ DCS1 *5 mM DMSO Solution* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM148.938 µL744.69 µL1.489 mL7.447 mL14.894 mL
5 mM29.788 µL148.938 µL297.876 µL1.489 mL2.979 mL
10 mM14.894 µL74.469 µL148.938 µL744.69 µL1.489 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

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Spectrum


Open in Advanced Spectrum Viewer
spectrum

Spectral properties

Excitation (nm)631
Emission (nm)651

Images


Citations


View all 9 citations: Citation Explorer
Nuclear translocation of Axl contributes to the malignancy of oral cancer cells
Authors: Su, Yu-Fu and Shen, Po-Chien and Huang, Wen-Yen and Hung, Yi-Jen and Huang, Tsai-Wang and Lin, Che-Yi and Shieh, Yi-Shing
Journal: Journal of Dental Sciences (2023)
Bezafibrate Exerts Neuroprotective Effects in a Rat Model of Sporadic Alzheimer’s Disease
Authors: Lin, Li-Fan and Jhao, Yun-Ting and Chiu, Chuang-Hsin and Sun, Lu-Han and Chou, Ta-Kai and Shiue, Chyng-Yann and Cheng, Cheng-Yi and Ma, Kuo-Hsing
Journal: Pharmaceuticals (2022): 109
Calcitonin induces bone formation by increasing expression of Wnt10b in osteoclasts in ovariectomy-induced osteoporotic rats
Authors: Hsiao, Chen-Yuan and Chen, Tien-Hua and Chu, Tzu-Hui and Ting, Yen-Nien and Tsai, Pei-Jiun and Shyu, Jia-Fwu
Journal: Frontiers in Endocrinology (2020): 613
Osteoclast-released Wnt-10b underlies cinacalcet related bone improvement in chronic kidney disease
Authors: Zheng, Cai-Mei and Hsu, Yung-Ho and Wu, Chia-Chao and Lu, Chien-Lin and Liu, Wen-Chih and Zheng, Jing-Quan and Lin, Yuh-Feng and Chiu, Hui-Wen and Chang, Tian-Jong and Shyu, Jia-Fwu and others,
Journal: International journal of molecular sciences (2019): 2800
Neural stem cells for disease modeling and evaluation of therapeutics for infantile (CLN1/PPT1) and late infantile (CLN2/TPP1) neuronal ceroid lipofuscinoses
Authors: Sima, Ni and Li, Rong and Huang, Wei and Xu, Miao and Beers, Jeanette and Zou, Jizhong and Titus, Steven and Ottinger, Elizabeth A and Marugan, Juan J and Xie, Xing and others, undefined
Journal: Orphanet journal of rare diseases (2018): 54
Synthesis of the Anionic Hydroxypropyl-&beta;-cyclodextrin: Poly (decamethylenephosphate) Polyrotaxane and Evaluation of its Cholesterol Efflux Potential in Niemann-Pick C1 Cells
Authors: Egele, Kerstin and Samaddar, Shayak and Schneider, Nina and Thompson, David H and Wenz, Gerhard
Journal: Journal of Materials Chemistry B (2018)
Methyl-$\beta$-cyclodextrin restores impaired autophagy flux in Niemann-Pick C1-deficient cells through activation of AMPK
Authors: Dai, Sheng and Dulcey, Andr{\'e}s E and Hu, Xin and Wassif, Christopher A and Porter, Forbes D and Austin, Christopher P and Ory, Daniel S and Marugan, Juan and Zheng, Wei
Journal: Autophagy (2017): 1435--1451
One-Step Seeding of Neural Stem Cells with Vitronectin-Supplemented Medium for High-Throughput Screening Assays
Authors: Dai, Sheng and Li, Rong and Long, Yan and Titus, Steve and Zhao, Jinghua and Huang, Ruili and Xia, Menghang and Zheng, Wei
Journal: Journal of Biomolecular Screening (2016): 1112--1124
Genome shuffling of the nonconventional yeast Pichia anomala for improved sugar alcohol production
Authors: Zhang, Guoqiang and Lin, Yuping and Qi, Xianni and Wang, Lixian and He, Peng and Wang, Qinhong and Ma, Yanhe
Journal: Microbial cell factories (2015): 1

References


View all 65 references: Citation Explorer
In vitro activity of pyrvinium pamoate against Entamoeba histolytica and Giardia intestinalis using radiolabelled thymidine incorporation and an SYBR Green I-based fluorescence assay
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Journal: J Antimicrob Chemother (2009): 751
Detection of methylation in hepatocellular carcinoma using SYBR Green fluorescent quantitative PCR
Authors: Yang B, Lou C, Gao Y, Du Z, Song W.
Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2008): 534
Estimation of copy number using SYBR Green: confounding by AT-rich DNA and by variation in amplicon length
Authors: Colborn JM, Byrd BD, Koita OA, Krogstad DJ.
Journal: Am J Trop Med Hyg (2008): 887
DRAQ5-based, no-lyse, no-wash bone marrow aspirate evaluation by flow cytometry
Authors: Allan RW, Ansari-Lari MA, Jordan S.
Journal: Am J Clin Pathol (2008): 706
Interaction of a DNA intercalator DRAQ5, and a minor groove binder SYTO17, with chromatin in live cells--influence on chromatin organization and histone-DNA interactions
Authors: Wojcik K, Dobrucki JW.
Journal: Cytometry A (2008): 555
Addition of gold nanoparticles to real-time PCR: effect on PCR profile and SYBR Green I fluorescence
Authors: Haber AL, Griffiths KR, Jamting AK, Emslie KR.
Journal: Anal Bioanal Chem (2008): 887
Tetraalkylammonium derivatives as real-time PCR enhancers and stabilizers of the qPCR mixtures containing SYBR Green I
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Journal: Nucleic Acids Res (2008): e93
Highly sensitive and selective detection of Hg(2+) in aqueous solution with mercury-specific DNA and Sybr Green I
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Journal: Chem Commun (Camb) (2008): 4759
Group testing to annihilate pairs applied to DNA cross-hybridization elimination using SYBR Green I
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DRAQ5: improved flow cytometric DNA content analysis and minimal residual disease detection in childhood malignancies
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