Cy5 maleimide (non-sulfonated)

Cy5 maleimide (non-sulfonated)

Catalog Number:
DAD1368215APE
Mfr. No.:
APE-A8139
Price:
$392
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      • Overview
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          Background

          Cy5 maleimide is a mono-reactive dye for selectively labeling peptides and proteins which couples with thiol groups. The labeling reagent is a common fluorophore dye with low aqueous solubility which is compatible with various instrumentation like microscopes, imagers, and fluorescence readers. Cy5 maleimide is part of the probe among the biological research. For biomolecule labeling, the labeling reagent has low aqueous solubility, using of organic co-solvent to dissolve this molecular is necessary for efficient reaction. First, Cyanine dye should be dissolved in organic solvent and then added to a solution of biomolecule in appropriate aqueous buffer. The user can generate probes with virtually any non-genetically encoded moiety of interest with the scaffold in hand.
          G3C(Cy5) probe consists of two parts. First, a GGGC scaffold peptide is synthesized on solid phase, followed by coupling of the liberated peptide to Cy5 maleimide, while in solution [1].


          Reference: [1]. Popp, M.W. Site-Specific Labeling of Proteins via Sortase: Protocols for the Molecular Biologist. Methods in Molecular Biology,2015, 1266, 185–198.

      • Properties
        • Categories
          Labeling of cysteine residues, as well as other thiolated molecules
          Alternative Name
          6-[(2E)-3,3-dimethyl-2-[(2E,4E)-5-(1,3,3-trimethylindol-1-ium-2-yl)penta-2,4-dienylidene]indol-1-yl]-N-[2-(2,5-dioxopyrrol-1-yl)ethyl]hexanamide
          Molecular Formula
          C38H45ClN4O3
          Molecular Weight
          641.24
          Appearance
          A solid
          Purity
          98.76%
          Solubility
          ≥64.1 mg/mL in DMSO; insoluble in H2O; ≥65 mg/mL in EtOH
          Storage
          24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate.
          SMILES
          CC1(C2=CC=CC=C2[N+](=C1C=CC=CC=C3C(C4=CC=CC=C4N3CCCCCC(=O)NCCN5C(=O)C=CC5=O)(C)C)C)C

          * For Research Use Only

      • Reference
        • 1. Xueting Tang, Lin Chen, et al. "Lipophilic NO-Driven Nanomotors as Drug Balloon Coating for the Treatment of Atherosclerosis." Small. 2022 Aug 12;e2203238. PMID:35961946
          2. Qi Wang , Ting Li, et al. "Engineered Exosomes with Independent Module/Cascading Function for Therapy of Parkinson's Disease by Multistep Targeting and Multistage Intervention Method." Adv Mater. 2022 Apr 18;e2201406. PMID:35435282
          3. Xiuhua Pan, Xiaochen Pei, et al. "One-in-one individual package and delivery of CRISPR/Cas9 ribonucleoprotein using apoferritin." J Control Release. 2021 Sep 10;337:686-697. PMID:34389365
          4. Bhatt R, Chudaev M, et al. "Engineered EF-Tu and tRNA-Based FRET Screening Assay to Find Inhibitors of Protein Synthesis in Bacteria." Assay Drug Dev Technol. 2018 May/Jun;16(4):212-221. PMID:29870274

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