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Fluorescein-12-dATP Sale

(Synonyms: Fluorescein-12-2’-deoxyadenosine-5’-triphosphate) 目录号 : GC49455

A fluorescently labeled form of dATP

Fluorescein-12-dATP Chemical Structure

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1 nmol
¥397.00
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5 nmol
¥1,681.00
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10 nmol
¥2,982.00
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25 nmol
¥5,948.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Fluorescein-12-dATP is a fluorescently labeled form of the nucleotide 2’-deoxyadenosine-5’-triphosphate . It displays excitation/emission maxima of 498/517 nm, respectively. Fluorescein-12-dATP has been used to label DNA in fluorescence in situ hybridization (FISH) and nicking enzyme-assisted viewing and sequencing (NicE-viewSeq) applications.1,2

1.EstÈve, P.-O., Vishnu, U.S., Chin, H.G., et al.Visualization and sequencing of accessible chromatin reveals cell cycle and PostHDAC inhibitor treatment dynamicsJ. Mol. Biol.432(19)5304-5321(2020) 2.Kasahara, K., Taguchi, T., Yamasaki, I., et al.Genetic alterations in prostate cancerHandbook of immunohistochemistry and in situ hybridization of human carcinomas, Volume 2: Molecular pathology, colorectal carcinoma, and prostate carcinoma2299-305(2005)

Chemical Properties

Cas No. N/A SDF Download SDF
别名 Fluorescein-12-2’-deoxyadenosine-5’-triphosphate
Canonical SMILES O=C(CCCCCNC(C1=CC=C(C(O)=O)C(C2=C(C=C3)C(OC4=C2C=CC(O)=C4)=CC3=O)=C1)=O)NCC#CC5=CN([C@]6([H])O[C@H](COP(OP(OP(O)(O)=O)(O)=O)(O)=O)[C@@H](O)C6)C7=C5C(N)=NC=N7.O=C(CCCCCNC(C8=CC=C(C9=C(C=C%10)C(OC%11=C9C=CC(O)=C%11)=CC%10=O)C(C(O)=O)=C8)=O)NCC#CC%12=CN([C@]%13([H])O[C@H](COP(OP(OP(O)(O)=O)(O)=O)(O)=O)[C@@H](O)C%13)C%14=C%12C(N)=NC=N%14
分子式 C41H41N6O19P3 分子量 1014.7
溶解度 Water: soluble 储存条件 -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 0.9855 mL 4.9276 mL 9.8551 mL
5 mM 0.1971 mL 0.9855 mL 1.971 mL
10 mM 0.0986 mL 0.4928 mL 0.9855 mL
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Research Update

NicE-viewSeq: An Integrative Visualization and Genomics Method to Detect Accessible Chromatin in Fixed Cells

Methods Mol Biol 2023;2611:293-302.PMID:36807075DOI:10.1007/978-1-0716-2899-7_16.

A novel genome-wide accessible chromatin visualization, quantitation, and sequencing method is described, which allows in situ fluorescence visualization and sequencing of the accessible chromatin in the mammalian cell. The cells are fixed by formaldehyde crosslinking, and processed using a modified nick translation method, where a nicking enzyme nicks one strand of DNA, and DNA polymerase incorporates biotin-conjugated dCTP, 5-methyl-dCTP, Fluorescein-12-dATP or Texas Red-5-dATP, dGTP, and dTTP. This allows accessible chromatin DNA to be labeled for visualization and on bead NGS library preparation. This technology allows cellular level chromatin accessibility quantification and genomic analysis of the epigenetic information in the chromatin, particularly accessible promoter, enhancers, nucleosome positioning, transcription factor occupancy, and other chromosomal protein binding.