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AB275055

NBD-X, SE

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(1 Publication)

MW 391.34 Da, Purity >90%. Lipophilic green fluorescent probe for labeling antibodies and proteins. X-spacer provides separation between dye and protein for increased sensitivity and reduced impact on protein function. Functional analog of the dinitrophenol (DNP) hapten. Fluorescence is quenched when bound by anti-DNP antibodies.
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Chemical Structure - NBD-X, SE (AB275055)
  • Chemical Structure

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Chemical Structure - NBD-X, SE (AB275055)

Chemical structure of NBD-X, SE, 145195-58-0

Key facts

CAS number

145195-58-0

Purity

>90%

Form

Solid

form

Molecular weight

391.34 Da

Molecular formula

C<sub>1</sub><sub>6</sub>H<sub>1</sub><sub>7</sub>N<sub>5</sub>O<sub>7</sub>

PubChem

10237523

Nature

Synthetic

Solubility

Soluble in DMSO

Biochemical name

Hexanoic acid, 6-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-, 2,5-dioxo-1-pyrrolidinyl ester

Biological description

Lipophilic green fluorescent probe for labeling antibodies and proteins. X-spacer provides separation between dye and protein for increased sensitivity and reduced impact on protein function. Functional analog of the dinitrophenol (DNP) hapten. Fluorescence is quenched when bound by anti-DNP antibodies.

Canonical smiles

C1CC(=O)N(C1=O)OC(=O)CCCCCNC2=CC=C(C3=NON=C23)[N+](=O)[O-]

InChi

InChI=1S/C16H17N5O7/c22-12-7-8-13(23)20(12)27-14(24)4-2-1-3-9-17-10-5-6-11(21(25)26)16-15(10)18-28-19-16/h5-6,17H,1-4,7-9H2

InChiKey

ULIVORQJLJKPHQ-UHFFFAOYSA-N

IUPAC Name

(2,5-dioxopyrrolidin-1-yl) 6-[(4-nitro-2,1,3-benzoxadiazol-7-yl)amino]hexanoate

Excitation/Emission

Ex: 460nm, Em: 540nm

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions
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Product protocols

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Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Chemistry and physics of lipids 151:125-8 PubMed18039471

2007

An efficient, one-pot synthesis of various ceramide 1-phosphates from sphingosine 1-phosphate.

Applications

Unspecified application

Species

Unspecified reactive species

Peter Nussbaumer,Valentin Hornillos,Michael Ghobrial,Thomas Ullrich
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