Production Scale Optimized for Labeling 1 mg Antibody Per Reaction
Buccutite™ Rapid PerCP Antibody Labeling Kits, designed for large-scale production, provide a streamlined approach for labeling antibodies with PerCP, APC, PE, and iFluor® tandem dyes. Compared to conventional protein-protein conjugation methods like the SMCC crosslinking technique, Buccutite™ conjugation is simple and more robust. Using a two-step mixing protocol, researchers can directly conjugate PerCP to any antibody or protein in less than 2 hours. Each Buccutite™ kit includes all the essential components for two labeling reactions and features a user-friendly, pre-packed spin column to maximize conjugate yield. Each Buccutite™ FOL-Activated PerCP vial provided in this kit is precisely formulated to label 1 mg of purified protein or antibody. Before labeling, it's important to remove stabilizing proteins like BSA from the sample and avoid using amine-rich buffers like Tris, which might disrupt the labeling process. PerCP is an intensely bright, red fluorescent phycobiliprotein with an excitation and emission maxima of ~477 nm and ~678 nm, respectively. With its large Stoke’s Shift and compatibility with blue laser excitation, PerCP forms an ideal combination with iFluor® 488 (or FITC) and PE for conducting one- to three-color analyses with just a single laser. PerCP conjugates are large complexes well-suited for cell surface labeling techniques, flow cytometry, spectral flow cytometry, and other immunoassays requiring high sensitivity but not photostability. With Buccuitte™ Rapid Antibody Labeling kits, researchers can directly label primary antibodies, eliminating the need for secondary antibodies and enhancing panel-building flexibility.
Development of constrictional microchannels and the recurrent neural network in single-cell protein analysis.
Authors:
Zhang, Ting and Chen, Xiao and Chen, Deyong and Wang, Junbo and Chen, Jian
Journal:
Frontiers in bioengineering and biotechnology (2023): 1195940
Whole blood no-lyse no-wash micromethod for the quantitative measurement of monocyte HLA-DR.
Authors:
Miatello, Jordi and Faivre, Valérie and Marais, Clémence and Raineau, Mégane and Payen, Didier and Tissieres, Pierre
Journal:
Cytometry. Part B, Clinical cytometry (2023)
Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis.
Authors:
Zhang, Linlin and Liu, Mengjia and Zhang, Meng and Ai, Junhong and Tian, Jiao and Wang, Ran and Xie, Zhengde
Journal:
Journal of visualized experiments : JoVE (2022)
Recombinant thrombomodulin attenuates hyper-inflammation and glycocalyx damage in a murine model of Streptococcus pneumoniae-induced sepsis.
Authors:
Watanabe, Eizo and Akamatsu, Toshinobu and Ohmori, Masaaki and Kato, Mayu and Takeuchi, Noriko and Ishiwada, Naruhiko and Nishimura, Rintaro and Hishiki, Haruka and Fujimura, Lisa and Ito, Chizuru and Hatano, Masahiko
Journal:
Cytokine (2022): 155723
Routine flow cytometry approach for the evaluation of solid tumor neoplasms and immune cells in minimally invasive samples.
Authors:
Quirós-Caso, Covadonga and Arias Fernández, Tamara and Fonseca-Mourelle, Ariana and Torres, Héctor and Fernández, Luis and Moreno-Rodríguez, Maria and Ariza-Prota, Miguel Ángel and López-González, Francisco Julián and Carvajal-Álvarez, Miguel and Alonso-Álvarez, Sara and Moro-García, Marco Antonio and Colado, Enrique