68321
Atto 390 azide
BioReagent, suitable for fluorescence, ≥90% (HPLC)
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About This Item
Fórmula empírica (Notação de Hill):
C28H41N5O6
Peso molecular:
543.66
Número MDL:
Código UNSPSC:
12352125
ID de substância PubChem:
NACRES:
NA.32
Produtos recomendados
linha de produto
BioReagent
Ensaio
≥90% (HPLC)
Formulário
solid
fabricante/nome comercial
ATTO-TEC GmbH
λ
in ethanol (with 0.1% trifluoroacetic acid)
Absorção UV
λ: 380-384 nm Amax
adequação
suitable for fluorescence
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
CC(CC(C)(C)N1CCCC(NCCOCCOCCOCCN=[N+]=[N-])=O)C2=C1C=C(OC(C=C3C)=O)C3=C2
InChI
1S/C28H41N5O6/c1-20-16-27(35)39-25-18-24-22(17-23(20)25)21(2)19-28(3,4)33(24)9-5-6-26(34)30-7-10-36-12-14-38-15-13-37-11-8-31-32-29/h16-18,21H,5-15,19H2,1-4H3,(H,30,34)
chave InChI
FEBSRHTZZIMYNR-UHFFFAOYSA-N
Descrição geral
Atto 390 is a fluorescent label with a coumarin structure. The dye is intended for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are high fluorescence quantum yield, large Stokes-shift, good photostability and low molecular weight.
The azide modification is suitable for reactions with alkyne groups (Huisgen reaction - “Click Chemistry“).
find more information here
The azide modification is suitable for reactions with alkyne groups (Huisgen reaction - “Click Chemistry“).
find more information here
Informações legais
This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Herein we report a method for the detection of methylated CpG dinucleotides located within CpG islands in genomic DNA using multiplexed bead-based assays and standard flow cytometry instrumentation. Four CpG "clusters" were identified in the TFPI2 and SPARC CpG islands
Gerhild Zauner et al.
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A fluorescence-based system to sense oxygen in solution is described. The method exploits the sensitivity of the endogenous fluorescence of type-3 copper proteins towards the presence of oxygen by translating the near-UV emission of the protein to label fluorescence in
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