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About This Item
Empirical Formula (Hill Notation):
C31H29BF2N4O6S
CAS Number:
Molecular Weight:
634.46
NACRES:
NA.21
SMILES string
O=C(CCCCCNC(COC1=CC=C(C2=CC=C3C=C4C=CC(C5=CC=CS5)=[N]4[B+3]([F-])([N-]32)[F-])C=C1)=O)ON6C(CCC6=O)=O
assay
≥95% (HPLC)
form
powder
color
, Red To very dark purple
solubility
DMSO: 2 mg/mL, clear
storage temp.
-10 to -25°C
Quality Level
Related Categories
Biochem/physiol Actions
Amine reactive, red luminous fluorescent labeling reagent that can be used to tag antibodies, proteins, peptides, and nucleic acids.
BODIPY TR-X NHS Ester is a versatile, amine-sensitive red fluorescent labeling reagent useful to tag antibodies, proteins, peptides, and nucleic acids. BODIPY TR dyes, also called boron-dipyrromethene tetramethylrhodamine, are known for their exceptional photophysical properties, including high fluorescence quality and photostability, with wide spectral tuning. BODIPY TR has a narrow absorption range (~ 500-550 nm) and a broader emission range (~ 580-640 nm) for multi-color cell labeling. BODIPY TR-X offers an extended excited-state lifetime for fluorescence polarization assays and significant two-photon excitation capability. BODIPY TR-X NHS Ester is a valuable tool for fluorescence microscopy, flow cytometry, and IHC applications.
BODIPY TR-X NHS Ester is a versatile, amine-sensitive red fluorescent labeling reagent useful to tag antibodies, proteins, peptides, and nucleic acids. BODIPY TR dyes, also called boron-dipyrromethene tetramethylrhodamine, are known for their exceptional photophysical properties, including high fluorescence quality and photostability, with wide spectral tuning. BODIPY TR has a narrow absorption range (~ 500-550 nm) and a broader emission range (~ 580-640 nm) for multi-color cell labeling. BODIPY TR-X offers an extended excited-state lifetime for fluorescence polarization assays and significant two-photon excitation capability. BODIPY TR-X NHS Ester is a valuable tool for fluorescence microscopy, flow cytometry, and IHC applications.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Highly potent and selective fluorescent antagonists of the human adenosine A? receptor based on the 1,2,4-triazolo[4,3-a]quinoxalin-1-one scaffold
Journal of Medicinal Chemistry, 55(4), 1771-1782 (2012)
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Nanoscale, 9(4), 1511-1519 (2017-01-10)
Förster resonant energy transfer (FRET) is a nonradiative process by which the energy of light absorbed by a donor molecule is transferred to an acceptor molecule over a distance of several nanometers. FRET plays a crucial role in photosynthesis and
Karen Martin et al.
Proteomics, 2(5), 499-512 (2002-05-03)
A two-color fluorescence detection method is described based upon covalently coupling the succinimidyl ester of BODIPY TR-X dye to proteins immobilized on polyvinylidene difluoride membranes, followed by detection of target proteins using the fluorogenic, precipitating substrate ELF 39-phosphate in combination
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