logo
AAT Bioquest

HIS Lite™ iFluor™ 568 Tris NTA Chelator

Product Image
Product Image
Gallery Image 1
Ordering information
Price
Catalog Number
Unit Size
Quantity
Add to cart
Additional ordering information
Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
ShippingStandard overnight for United States, inquire for international
Request quotation
Physical properties
Molecular weight1541.63
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.34
Correction Factor (280 nm)0.15
Extinction coefficient (cm -1 M -1)1000001
Excitation (nm)568
Emission (nm)587
Quantum yield0.571
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure

OverviewpdfSDSpdfProtocol


Molecular weight
1541.63
Correction Factor (260 nm)
0.34
Correction Factor (280 nm)
0.15
Extinction coefficient (cm -1 M -1)
1000001
Excitation (nm)
568
Emission (nm)
587
Quantum yield
0.571
iFluor® 568 Tris-NTA Chelator is used as a sensitive fluorescent probe for detecting polyhistidine-labeled proteins in combination with the addition of a heavy metal ion( such as Ni2+) in cells, solution and solid surfaces. Fluorescent tris-NTA compounds provide an efficient method for site-specific and stable noncovalent fluorescence labeling of polyhistidine-tagged proteins. In combination with OG488-tris-NTA compound iFluor® 568 Tris-NTA can be used for multicolor analysis of polyhistidine-tagged proteins. In contrast to the transient binding of conventional mono-NTA, the multivalent interaction of tris-NTA conjugated fluorophores form a much more stable complex with polyhistidine-tagged proteins. The high selectivity of tris-NTA compounds toward cumulated histidines enables the selective labeling of proteins in cell lysates and on the surface of live cells. Fluorescent tris-NTA conjugates can be applied for the analysis of a ternary protein complex in solution and on surfaces. AAT Bioquest also offers HIS Lite™ iFluor™ 568 Tris NTA-Ni Complex that can be directly used for the specific and highly sensitive detection of His-tagged fusion proteins without the addition of a heavy metal ion. The transition metal ions (e.g., Ni ion)-mediated complexation of polyhistidine-labeled proteins with fluorescent tris-NTA conjugates provides a sensitive reporter for detecting and monitoring protein-protein interactions in real time.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of HIS Lite™ iFluor™ 568 Tris NTA Chelator to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM64.866 µL324.332 µL648.664 µL3.243 mL6.487 mL
5 mM12.973 µL64.866 µL129.733 µL648.664 µL1.297 mL
10 mM6.487 µL32.433 µL64.866 µL324.332 µL648.664 µL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
/=x=

Spectrum


Open in Advanced Spectrum Viewer
spectrum

Spectral properties

Correction Factor (260 nm)0.34
Correction Factor (280 nm)0.15
Extinction coefficient (cm -1 M -1)1000001
Excitation (nm)568
Emission (nm)587
Quantum yield0.571

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)Correction Factor (656 nm)
HIS Lite™ iFluor™ 647 Tris NTA Chelator65667025000010.2510.030.030.0793

Images


References


View all 33 references: Citation Explorer
Engineering Protein Nanoparticles Functionalized with an Immunodominant Coxiella burnetii Antigen to Generate a Q Fever Vaccine.
Authors: Ramirez, Aaron and Felgner, Jiin and Jain, Aarti and Jan, Sharon and Albin, Tyler J and Badten, Alexander J and Gregory, Anthony E and Nakajima, Rie and Jasinskas, Algimantas and Felgner, Philip L and Burkhardt, Amanda M and Davies, D Huw and Wang, Szu-Wen
Journal: Bioconjugate chemistry (2023): 1653-1666
Protein Nanoparticle-Mediated Delivery of Recombinant Influenza Hemagglutinin Enhances Immunogenicity and Breadth of the Antibody Response.
Authors: Badten, Alexander J and Ramirez, Aaron and Hernandez-Davies, Jenny E and Albin, Tyler J and Jain, Aarti and Nakajima, Rie and Felgner, Jiin and Davies, D Huw and Wang, Szu-Wen
Journal: ACS infectious diseases (2023): 239-252
A Four-Channel Surface Plasmon Resonance Sensor Functionalized Online for Simultaneous Detections of Anti-SARS-CoV-2 Antibody, Free Viral Particles, and Neutralized Viral Particles.
Authors: Dong, Tianbao and Han, Chaowei and Jiang, Meng and Zhang, Tiantian and Kang, Qing and Wang, Pengcheng and Zhou, Feimeng
Journal: ACS sensors (2022): 3560-3570
Regenerable and high-throughput surface plasmon resonance assay for rapid screening of anti-SARS-CoV-2 antibody in serum samples.
Authors: Jiang, Meng and Dong, Tianbao and Han, Chaowei and Liu, Luyao and Zhang, Tiantian and Kang, Qing and Wang, Pengcheng and Zhou, Feimeng
Journal: Analytica chimica acta (2022): 339830
Facile Method of Tubulin Purification from Goat Brain for Reconstitution of Microtubule-Associated Intracellular Function.
Authors: Ghosh, Satyajit and Garg, Shubham and Mukherjee, Nabanita and Ghosh, Surajit
Journal: Methods in molecular biology (Clifton, N.J.) (2022): 17-45
Rapid and regenerable surface plasmon resonance determinations of biomarker concentration and biomolecular interaction based on tris-nitrilotriacetic acid chips.
Authors: Liu, Luyao and Han, Chaowei and Jiang, Meng and Zhang, Tiantian and Kang, Qing and Wang, Xiaoying and Wang, Pengcheng and Zhou, Feimeng
Journal: Analytica chimica acta (2021): 338625
Quantifying the Interaction of Phosphite with ABC Transporters: MicroScale Thermophoresis and a Novel His-Tag Labeling Approach.
Authors: Bartoschik, Tanja and Gupta, Amit and Kern, Beate and Hitchcock, Andrew and Adams, Nathan B P and Tschammer, Nuska
Journal: Methods in molecular biology (Clifton, N.J.) (2020): 51-62
Near-native, site-specific and purification-free protein labeling for quantitative protein interaction analysis by MicroScale Thermophoresis.
Authors: Bartoschik, Tanja and Galinec, Stefanie and Kleusch, Christian and Walkiewicz, Katarzyna and Breitsprecher, Dennis and Weigert, Sebastian and Muller, Yves A and You, Changjiang and Piehler, Jacob and Vercruysse, Thomas and Daelemans, Dirk and Tschammer, Nuska
Journal: Scientific reports (2018): 4977
Docking of Antibodies into the Cavities of DNA Origami Structures.
Authors: Ouyang, Xiangyuan and De Stefano, Mattia and Krissanaprasit, Abhichart and Bank Kodal, Anne Louise and Bech Rosen, Christian and Liu, Tianqiang and Helmig, Sarah and Fan, Chunhai and Gothelf, Kurt V
Journal: Angewandte Chemie (International ed. in English) (2017): 14423-14427
Affinity Capturing and Surface Enrichment of a Membrane Protein Embedded in a Continuous Supported Lipid Bilayer.
Authors: Gunnarsson, Anders and Simonsson Nyström, Lisa and Burazerovic, Sabina and Gunnarsson, Jenny and Snijder, Arjan and Geschwindner, Stefan and Höök, Fredrik
Journal: ChemistryOpen (2016): 445-449