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Product Description

Fluoppi is a technology providing an easy way to visualize protein-protein interactions (PPIs) with a high signal to noise ratio. It employs an oligomeric assembly helper tag (Ash-tag) and a tetrameric fluorescent protein tag (FP-tag) to create detectable fluorescent foci when there are interactions between two proteins fused to the tags. By way of example, genetic fusion of protein X with FP-tag, and Y with Ash-tag creates a tetrameric fluorescent fusion protein X-FP and an oligomeric fusion protein Y-Ash respectively. Because each fusion protein has multiple Xs or Ys, interaction between X and Y causes large lattice like complexes where the fluorescence by X-FP is concentrated and detectable as fluorescent foci. Anti-Ash-tag monoclonal antibody (mAb) recognizes the joint region between Ash-tag and flexible linker . Fluoppi Ver.2 : Ash-Red contains an additional amino acid at the C terminal of Ash-tag expressed by pAsh-MNL, which make it possible to be recognized by the mAbFluoppi Ver.2 : Ash-Red includes 4 expression plasmids as listed in section 2. A tetrameric red fluorescent protein, Monti-Red, is employed as a FP-tag as describe




Documents & Links for Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL)
Datasheet Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL) Datasheet
Purchase Agreement Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL) Purchase Agreement

Documents & Links for Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL)
Datasheet Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL) Datasheet
Purchase Agreement Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL) Purchase Agreement
Citations for Fluoppi Ver.2: Ash-Red (Ash-MNL/MCL + Monti-Red-MNL/MCL) – 6 Found
Koyano, Fumika; Okatsu, Kei; Kosako, Hidetaka; Tamura, Yasushi; Go, Etsu; Kimura, Mayumi; Kimura, Yoko; Tsuchiya, Hikaru; Yoshihara, Hidehito; Hirokawa, Takatsugu; Endo, Toshiya; Fon, Edward A; Trempe, Jean-François; Saeki, Yasushi; Tanaka, Keiji; Matsuda, Noriyuki. Ubiquitin is phosphorylated by PINK1 to activate parkin. Nature. 2014;510(7503):162-6.  PubMed
Yamano, Koji; Queliconi, Bruno B; Koyano, Fumika; Saeki, Yasushi; Hirokawa, Takatsugu; Tanaka, Keiji; Matsuda, Noriyuki. Site-specific Interaction Mapping of Phosphorylated Ubiquitin to Uncover Parkin Activation. The Journal Of Biological Chemistry. 2015;290(42):25199-211.  PubMed
Asamitsu, Kaori; Omagari, Katsumi; Okuda, Tomoya; Hibi, Yurina; Okamoto, Takashi. Quantification of the HIV transcriptional activator complex in live cells by image-based protein-protein interaction analysis. Genes To Cells : Devoted To Molecular & Cellular Mechanisms. 2016;21(7):706-16.  PubMed
Watanabe, Taku; Seki, Tatsuya; Fukano, Takashi; Sakaue-Sawano, Asako; Karasawa, Satoshi; Kubota, Misaki; Kurokawa, Hiroshi; Inoue, Ken; Akatsuka, Junichi; Miyawaki, Atsushi. Genetic visualization of protein interactions harnessing liquid phase transitions. Scientific Reports. 2017;7:46380.  PubMed
Saito, Ken; Iioka, Hidekazu; Maruyama, Satoshi; Sumardika, I Wayan; Sakaguchi, Masakiyo; Kondo, Eisaku. PODXL1 promotes metastasis of the pancreatic ductal adenocarcinoma by activating the C5aR/C5a axis from the tumor microenvironment. Neoplasia (New York, N.y.). 2019;21(12):1121-1132.  PubMed
Yoshikawa, Masaru; Yoshii, Tatsuyuki; Ikuta, Masahiro; Tsukiji, Shinya. Synthetic Protein Condensates That Inducibly Recruit and Release Protein Activity in Living Cells. Journal Of The American Chemical Society. 2021;143(17):6434-6446.  PubMed


Documentation Requirements for Order Placement

Material Transfer or Licensing Agreement (MTA)
The manufacturer of this product requires a signed Material Transfer or Licensing Agreement to be submitted at time of order placement. Access the agreement in the Documents section below. Please download and fill in the document as requested. Submit the completed document with your order to orders@cosmobiousa.com.