qFlamma® Black01 Carboxylic acid

Product#: QWC1001
$778.24

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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qFlamma® Black01 Carboxylic acid

Cat. No. List below

Description

qFlamma® Black01 Carboxylic acid is an inactive form of universal dark quencher that the range of absorption covers from 400 to 800 nm with no native fluorescence. Black01 quencher displays high absorption coefficient, superb stability and aqueous solubility. A hexanoic acid is attached to Black01 quencher. qFlamma® Black01 carboxylic acid can be coupled with amines at a probe or on biomolecules by standard amide bond coupling conditions or can be utilized as a reference standard for fluorophore-quencher pair probes. 
 
Specifications
  • Functionality: Dark quencher
  • Functional group: carboxylic acid
  • Absorption max. (nm): 484
  • Absorption range (nm): 400 ~ 800
  • Extinction coefficient: ≥ 12,000 cm-1M-1
  • Appearance: Green Solid
  • Molecular Weight: 721.76 g/mol
  • Solubility: Water, DMF
  • Storage conditions: 4 ℃, protect from light

 qFlamma® Quenchers
 
Quick link (Cat.#) Series Quick link (Cat.#) Series
QWS1001 qFlamma® Black01 NHS ester QWSN1001 qFlamma® Black01 Sulfo-NHS ester
QWA1001 qFlamma® Black01 Vinylsulfone QWC1001 qFlamma® Black01 Carboxylic acid
QWM1001 qFlamma® Black01 Maleimide QWE1001 qFlamma® Black01 Amine
QWT1001 qFlamma® Black01 Thiol QWR1001 qFlamma® Black01 Dichlorotriazine
QWG1001 qFlamma® Black01 PEG4-Alkyne QWD1001 qFlamma® Black01 ADIBO
QWB1001 qFlamma® Black01 Biotin QWK1001 qFlamma® Black01 Alkyne
QWZ1001 qFlamma® Black01 Azide QWH1001 qFlamma® Black01 Hydrazide


Background

qFlamma® Quenchers

Dark quenchers are substances that absorb excitation energy from a fluorophore and dissipate the energy as heat without any native fluorescence. The combination of a fluorescent dye and quencher may act as an on/off switch of fluorescence that the original fluorescence might be restored as the distance between them increases or when their connection is cleaved. In conjunction with fluorophores, dark quenchers are regarded as key components in designing FRET probes, in protease activity assays, nucleic acid hybridization, PCR, etc. The main advantage of dark quencher is the non-emissive excitation and elimination of background fluorescence. BioActs developed a new generation of azo-anthraquinone derivative dark quenchers, qFlamma® quenchers, to overcome issues associated with existing dark quenchers such as stability, quenching ability and water solubility.

The absorbance peaks of qFlamma® quenchers completely cover spectral range from visible to near-infrared (NIR) that all of commercially available fluorescent dyes can be effectively quenched. The quenchers display high absorption coefficient together with excellent quenching ability, superb stability and aqueous solubility so that it can easily manipulated in aqueous buffers. The four of qFlamma® quenchers (Black 01, Red, Blue and Orange) series cover the electromagnetic spectrum from 400 nm to NIR region and provides excellent spectral overlap across the entire range of known fluorescent dyes. The complete spectral overlap of qFlamma® quencher series along with their variety of reacting groups enable to design single-tube multiplexing assay system owing their capability for efficient quenching and the preventing cross-talking between dyes. BioActs offers qFlamma® quenchers as universal dark quenchers for the construction of a variety of hybridization and custom-synthesized probes incorporated spectrally paired fluorophores and quenchers for multiplexed bio-analysis, PCR, nucleic acid hybridization, and high-throughput imaging assays.
 
  • Completely dissipate fluorescent energy without native fluorescence
  • Can quench all of commercially available fluorescent dyes
  • High absorption coefficient, excellent quenching ability, superb stability and aqueous solubility
  • High purity and compatible with most of biomolecules.

 

Types of qFlamma® Quenchers

 

 

Figure 1.  Absorption spectra of 4 qFlamma® quenchers with emission maxima of commonly used fluorescent dyes.


Citation & Reference

1. Arnaud Chevalier. Bioconjugatable Azo-Based Dark-Quencher Dyes: Synthesis and Application to Protease-Activatable Far-Red Fluorescent Probes. Chemistry 19.5 (2013): 1686-99.

2. Arnaud Chevalier. Universal Dark Quencher Based on “Clicked” Spectrally Distinct Azo Dyes. Org. Lett 2013 15.23 (2013): 6082–6085.

3. Arnaud Chevalier. Straightforward synthesis of bioconjugatable azo dyes. Part 1: Black Hole Quencher-1 (BHQ-1) scaffold. Tetrahedron Letters 55.50 (2014): 6759-6763.

 

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