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AAT Bioquest

CDPI3 Azide [Minor Groove Binder Azide]

Minor Groove Binder (MGB) molecules selectively bind to the minor groove of a DNA molecule, the shallow furrow in the DNA helix. MGB-labeled oligonucleotides form stable hybrid complexes with complementary DNA and RNA target sequences. Dihydropyrroloindole tripeptide (CDPI3), the analogs of natural product CC-1065, have been shown to arrest sequence-specific primer extension on single-stranded DNA when linked to oligonucleotides. CDPI3-containing oligonucleotides increases both the specificity and the strength of hybridization, thus enhancing the stability of DNA duplexes. The addition of MGB molecules to DNA probes allows the design of shorter hybridization probes useful for molecular diagnostics, e.g., quantitative PCR based assays. Several designs are possible, including Taqman MGB probes. Compared to other commercial MGB probes, AAT Bioquest offer this MGB building block that contains a methylpiperazine moiety (derived from Hoechst 33258, another popular MGB molecule) to further enhance its DNA affinity. We offer CDPI3 azide for labeling alkyne-modified oligos.

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Correction Factor (280 nm)
AMCA Azide346434190000.153
XFD488 azide *Same Structure to Alexa Fluor™ 488 azide*499520710000.11
ICG azide7898132300000.076
Cy3B azide56057112000010.069
XFD647 Azide6506712700000.03
XFD350 azide343441190000.19
XFD405 azide40142135,0000.70
XFD430 azide43254015,0000.28
XFD514 azide518543800000.18
XFD546 azide5615721120000.12
XFD532 azide534553810000.09
XFD568 azide579603913000.46
XFD594 azide590618900000.56
Show More (4)

References

View all 5 references: Citation Explorer
Synthesis and biological evaluation of a novel betulinic acid derivative as an inducer of apoptosis in human colon carcinoma cells (HT-29).
Authors: Chakraborty, Biswajit and Dutta, Debasmita and Mukherjee, Sanjukta and Das, Supriya and Maiti, Nakul C and Das, Padma and Chowdhury, Chinmay
Journal: European journal of medicinal chemistry (2015): 93-105
Novel metal-based pharmacologically dynamic agents of transition metal(II) complexes: designing, synthesis, structural elucidation, DNA binding and photo-induced DNA cleavage activity.
Authors: Raman, N and Jeyamurugan, R and Sakthivel, A and Mitu, L
Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy (2010): 88-97
Synthesis, crystal structure, DNA binding and photo-induced DNA cleavage activity of (S-methyl-L-cysteine)copper(II) complexes of heterocyclic bases.
Authors: Patra, Ashis K and Nethaji, Munirathinam and Chakravarty, Akhil R
Journal: Journal of inorganic biochemistry (2007): 233-44
Syntheses, crystal structures, and oxidative DNA cleavage of some Cu(II) complexes of 5-amino-3-pyridin-2-yl-1,2,4-triazole.
Authors: Ferrer, Sacramento and Ballesteros, Rafael and Sambartolomé, Ana and González, Marta and Alzuet, Gloria and Borrás, Joaquín and Liu, Malva
Journal: Journal of inorganic biochemistry (2004): 1436-46
Metal-assisted light-induced DNA cleavage activity of 2-(methylthio)phenylsalicylaldimine Schiff base copper(II) complexes having planar heterocyclic bases.
Authors: Reddy, Pattubala A N and Santra, Bidyut K and Nethaji, Munirathinam and Chakravarty, Akhil R
Journal: Journal of inorganic biochemistry (2004): 377-86
Page updated on November 21, 2024

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Catalog Number6909
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Physical properties

Molecular weight

1434.66

Solvent

DMSO

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501