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sulfocyanine5 5  (Lumiprobe)


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    Structured Review

    Lumiprobe sulfocyanine5 5
    Sulfocyanine5 5, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 94/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cyanine5+5+azide/Sulfo-Cyanine5%2E5+azide/pm41930901-56-43-46
    Average 94 stars, based on 9 article reviews
    sulfocyanine5 5 - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    other:

    Article Title: Zwitterionic Cross-Linked Biodegradable Nanocapsules for Cancer Imaging
    Article Snippet: Cyanine5.5 azide (Cy5.5-N3) was purchased from Lumiprobe Corporation.

    Article Title: Identification of a novel target of sulforaphane: Sulforaphane binds to acyl-protein thioesterase 2 (APT2) and attenuates its palmitoylation.
    Article Snippet: The anti-FLAG M2 affinity gel and NH2OH were purchased from Sigma (St Louis, MO, USA) and cyanine5.5 azide from Lumiprobe Limited (Wan Chai, Hong Kong).

    Article Title: Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions.
    Article Snippet: Cyanine5.5 azide and Cyanine5 NHS ester were purchased from Lumiprobe.

    Article Title: Methods and compositions for detecting hematopoietic and lymphoid tissue cancer cells
    Article Snippet: Examples of azide containing probe compounds include BDP FL azide, BDP TMR azide, Coumarin 343 azide, Coumarin 343 X azide, Cyanine3 azide, Cyanine3.5 azide, Cyanine5 azide, Cyanine5.5 azide, Cyanine7 azide, Cyanine7.5 azide, FAM azide, 5-isomer, FAM azide, 6-isomer, PEP azide, Perylene azide, Pyrene azide 1, Pyrene azide 2, Pyrene azide 3, ROX azide, 5-isomer, Sulfo-Cyanine3 azide, Sulfo-Cyanine5 azide, Sulfo-Cyanine5.5 azide, Sulfo-Cyanine7 azide, TAMRA azide, 5-isomer, which are commercially available from Lumiprobe Corporation located in Hallandale Beach Fla.

    Droplet Countercurrent Chromatography:

    Article Title: Therapeutic Delivery of Polymeric Tadpole Nanostructures with High Selectivity to Triple Negative Breast Cancer Cells.
    Article Snippet: Subscriber access provided by University of Massachusetts Amherst Libraries is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society.

    Article Title: RGD Density on Tadpole Nanostructures Regulates Cancer Stem Cell Proliferation and Stemness.
    Article Snippet: Cancer stem cells (CSCs) make up a small population of cancer cells, primarily responsible for tumor initiation, metastasis, and drug resistance.. They overexpress Arg-Gly-Asp (RGD) binding integrin receptors that play crucial roles in cell proliferation and stemness through interaction with the extracellular matrix.. Here, we showed that monodisperse polymeric tadpole nanoparticles covalently coupled with different RGD densities regulated colon CSC proliferation and stemness in a RGD density-dependent manner.

    Labeling:

    Article Title: Bioorthogonal PEGylation Prolongs the Elimination Half-Life of N-TIMP2 While Retaining MMP Inhibition.
    Article Snippet: Tissue inhibitors of metalloproteinases (TIMPs) are natural inhibitors of the matrix metalloproteinase (MMP) family of proteins, whose members are key regulators of the proteolysis of extracellular matrix components and hence of multiple biological processes.. In particular, imbalanced activity of matrix metalloproteinase-14 (MMP-14) may lead to the development of cancer and cardiovascular and other diseases.. This study aimed to engineer TIMP2, one of the four homologous TIMPs, as a potential therapeutic by virtue of its ability to bind to the active-site Zn of MMP-14.



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    Lumiprobe cyanine5 5 n3
    Conjugation and characterization of EVs. (A) Schematic diagram of conjugating c(RGDyK), RKK12 <t>peptides,</t> <t>and</t> <t>Cyanine-5.5</t> dye to EVs by a two-step. (B) Expression of exosomal marker, CD63, CD9, CD81, and TSG101 from MSCs and Naïve or conjugated EVs. (C) Size distributions of Naïve and conjugated EVs based on Nano particle Tracking Analysis (NTA). (D) Transmission electron micrograph (TEM) images of Naïve and conjugated EVs. Scale bar, 100 nm. (E) Verification of the expression of integrin family proteins in R28 and CCD-986SK cells. (F) Uptake analysis of <t>Cy5.5-labeld</t> EVs in R28 cells. Cells were incubated with 100 μg/mL of Cy5.5-labeled EVs. Confocal microscopy demonstrated the presence of Cy5.5-labeled EVs in cells after 1 or 24 h of incubation. Magnification × 400. (G) Flow cytometric analyses of R28 cells (control) or Cy5.5_Naïve EVs, or c(RGDyK)_EVs. Cy5.5-c(RGDyK)-EVs were added with free c(RGDyK) peptide. (H) Zeta potential measurements were performed after peptide conjugation. (* P < .05, ** P < .01). All figures are original and were created by the authors.
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    Image Search Results


    Conjugation and characterization of EVs. (A) Schematic diagram of conjugating c(RGDyK), RKK12 peptides, and Cyanine-5.5 dye to EVs by a two-step. (B) Expression of exosomal marker, CD63, CD9, CD81, and TSG101 from MSCs and Naïve or conjugated EVs. (C) Size distributions of Naïve and conjugated EVs based on Nano particle Tracking Analysis (NTA). (D) Transmission electron micrograph (TEM) images of Naïve and conjugated EVs. Scale bar, 100 nm. (E) Verification of the expression of integrin family proteins in R28 and CCD-986SK cells. (F) Uptake analysis of Cy5.5-labeld EVs in R28 cells. Cells were incubated with 100 μg/mL of Cy5.5-labeled EVs. Confocal microscopy demonstrated the presence of Cy5.5-labeled EVs in cells after 1 or 24 h of incubation. Magnification × 400. (G) Flow cytometric analyses of R28 cells (control) or Cy5.5_Naïve EVs, or c(RGDyK)_EVs. Cy5.5-c(RGDyK)-EVs were added with free c(RGDyK) peptide. (H) Zeta potential measurements were performed after peptide conjugation. (* P < .05, ** P < .01). All figures are original and were created by the authors.

    Journal: Stem Cells Translational Medicine

    Article Title: Extracellular vesicles conjugated with c(RGDyk) peptide targeting integrin αVβ3 repair optic nerve injury through YAP/TAZ and Smad2/3 signaling

    doi: 10.1093/stcltm/szag006

    Figure Lengend Snippet: Conjugation and characterization of EVs. (A) Schematic diagram of conjugating c(RGDyK), RKK12 peptides, and Cyanine-5.5 dye to EVs by a two-step. (B) Expression of exosomal marker, CD63, CD9, CD81, and TSG101 from MSCs and Naïve or conjugated EVs. (C) Size distributions of Naïve and conjugated EVs based on Nano particle Tracking Analysis (NTA). (D) Transmission electron micrograph (TEM) images of Naïve and conjugated EVs. Scale bar, 100 nm. (E) Verification of the expression of integrin family proteins in R28 and CCD-986SK cells. (F) Uptake analysis of Cy5.5-labeld EVs in R28 cells. Cells were incubated with 100 μg/mL of Cy5.5-labeled EVs. Confocal microscopy demonstrated the presence of Cy5.5-labeled EVs in cells after 1 or 24 h of incubation. Magnification × 400. (G) Flow cytometric analyses of R28 cells (control) or Cy5.5_Naïve EVs, or c(RGDyK)_EVs. Cy5.5-c(RGDyK)-EVs were added with free c(RGDyK) peptide. (H) Zeta potential measurements were performed after peptide conjugation. (* P < .05, ** P < .01). All figures are original and were created by the authors.

    Article Snippet: Cyanine 5.5 azide (Cy5.5 azide; Lumiprobe Co., Hallandale Beach, FL, USA) was also introduced onto peptide-conjugated EVs according to the manufacturer’s protocol.

    Techniques: Conjugation Assay, Expressing, Marker, Transmission Assay, Incubation, Labeling, Confocal Microscopy, Control, Zeta Potential Analyzer