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secondary antibodies cy3 conjugated goat anti mouse lgg  (Proteintech)


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    Structured Review

    Proteintech secondary antibodies cy3 conjugated goat anti mouse lgg
    DPC-Exos transported miR-218-5p from DPCs to HFSCs. (A) Fluorescence imaging of HFSCs after treatment with DiI-labeled DPC-Exos (scale bar = 50 μm). (B) Schematic of the DPC–HFSC co-culture system with fluorescence showing intercellular transfer of exosomal miR-218–5p. (C) MiR-218–5p expression in HFSCs after transfection with <t>Cy3-miR-218–5p</t> (unpaired two-tailed t -test, n = 3). (D) MiR-218–5p expression in HFSCs after DPCs were transfected with siRNA-Drosha (unpaired two-tailed t -test, n = 3). (E) MiR-218–5p expression in HFSCs after DPCs were treated with GW4869 (unpaired two-tailed t -test, n = 3). ∗∗ P < 0.01.
    Secondary Antibodies Cy3 Conjugated Goat Anti Mouse Lgg, supplied by Proteintech, used in various techniques. Bioz Stars score: 97/100, based on 284 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/secondary antibodies cy3 conjugated goat anti mouse lgg/product/Proteintech
    Average 97 stars, based on 284 article reviews
    secondary antibodies cy3 conjugated goat anti mouse lgg - by Bioz Stars, 2026-06
    97/100 stars

    Images

    1) Product Images from "Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development"

    Article Title: Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development

    Journal: Non-coding RNA Research

    doi: 10.1016/j.ncrna.2026.01.004

    DPC-Exos transported miR-218-5p from DPCs to HFSCs. (A) Fluorescence imaging of HFSCs after treatment with DiI-labeled DPC-Exos (scale bar = 50 μm). (B) Schematic of the DPC–HFSC co-culture system with fluorescence showing intercellular transfer of exosomal miR-218–5p. (C) MiR-218–5p expression in HFSCs after transfection with Cy3-miR-218–5p (unpaired two-tailed t -test, n = 3). (D) MiR-218–5p expression in HFSCs after DPCs were transfected with siRNA-Drosha (unpaired two-tailed t -test, n = 3). (E) MiR-218–5p expression in HFSCs after DPCs were treated with GW4869 (unpaired two-tailed t -test, n = 3). ∗∗ P < 0.01.
    Figure Legend Snippet: DPC-Exos transported miR-218-5p from DPCs to HFSCs. (A) Fluorescence imaging of HFSCs after treatment with DiI-labeled DPC-Exos (scale bar = 50 μm). (B) Schematic of the DPC–HFSC co-culture system with fluorescence showing intercellular transfer of exosomal miR-218–5p. (C) MiR-218–5p expression in HFSCs after transfection with Cy3-miR-218–5p (unpaired two-tailed t -test, n = 3). (D) MiR-218–5p expression in HFSCs after DPCs were transfected with siRNA-Drosha (unpaired two-tailed t -test, n = 3). (E) MiR-218–5p expression in HFSCs after DPCs were treated with GW4869 (unpaired two-tailed t -test, n = 3). ∗∗ P < 0.01.

    Techniques Used: Fluorescence, Imaging, Labeling, Co-Culture Assay, Expressing, Transfection, Two Tailed Test



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    Image Search Results


    DPC-Exos transported miR-218-5p from DPCs to HFSCs. (A) Fluorescence imaging of HFSCs after treatment with DiI-labeled DPC-Exos (scale bar = 50 μm). (B) Schematic of the DPC–HFSC co-culture system with fluorescence showing intercellular transfer of exosomal miR-218–5p. (C) MiR-218–5p expression in HFSCs after transfection with Cy3-miR-218–5p (unpaired two-tailed t -test, n = 3). (D) MiR-218–5p expression in HFSCs after DPCs were transfected with siRNA-Drosha (unpaired two-tailed t -test, n = 3). (E) MiR-218–5p expression in HFSCs after DPCs were treated with GW4869 (unpaired two-tailed t -test, n = 3). ∗∗ P < 0.01.

    Journal: Non-coding RNA Research

    Article Title: Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development

    doi: 10.1016/j.ncrna.2026.01.004

    Figure Lengend Snippet: DPC-Exos transported miR-218-5p from DPCs to HFSCs. (A) Fluorescence imaging of HFSCs after treatment with DiI-labeled DPC-Exos (scale bar = 50 μm). (B) Schematic of the DPC–HFSC co-culture system with fluorescence showing intercellular transfer of exosomal miR-218–5p. (C) MiR-218–5p expression in HFSCs after transfection with Cy3-miR-218–5p (unpaired two-tailed t -test, n = 3). (D) MiR-218–5p expression in HFSCs after DPCs were transfected with siRNA-Drosha (unpaired two-tailed t -test, n = 3). (E) MiR-218–5p expression in HFSCs after DPCs were treated with GW4869 (unpaired two-tailed t -test, n = 3). ∗∗ P < 0.01.

    Article Snippet: After three times washing with PBS containing 0.1 % Tween-20 (Solarbio, China, Cat. No. ST825), secondary antibodies Cy3-conjugated Goat Anti-Mouse lgG (Proteintech, China, Cat No. SA00009-1) and Fluorescein (FlTc)-conjugated Goat Anti-Mouse lgG (Proteintech, China, Cat No. SA00003-1) were applied for incubation.

    Techniques: Fluorescence, Imaging, Labeling, Co-Culture Assay, Expressing, Transfection, Two Tailed Test

    Average Cy3 fluorescence intensity of silver nanostructured surfaces under different substrate inclination angles and withdrawal flow rates ( a – d ), along with the corresponding line plot ( e ) and three-dimensional bar chart ( f ).

    Journal: Biosensors

    Article Title: Angle-Dependent Dip Coating Strategy for Silver Nanostructured Surface Fabrication with Enhanced Fluorescence and Surface-Enhanced Raman Scattering Properties

    doi: 10.3390/bios16050292

    Figure Lengend Snippet: Average Cy3 fluorescence intensity of silver nanostructured surfaces under different substrate inclination angles and withdrawal flow rates ( a – d ), along with the corresponding line plot ( e ) and three-dimensional bar chart ( f ).

    Article Snippet: Cy3 and Rhodamine 6G (R6G) were used as probe molecules and purchased from Macklin Biochemical Co., Ltd. (Shanghai, China).

    Techniques: Fluorescence

    ( a , b ) Average fluorescence intensities of Cy3 at different concentrations on silver nanostructured surfaces and a glass slide; ( c ) fluorescence enhancement factor of the silver nanostructured surfaces relative to the glass slide.

    Journal: Biosensors

    Article Title: Angle-Dependent Dip Coating Strategy for Silver Nanostructured Surface Fabrication with Enhanced Fluorescence and Surface-Enhanced Raman Scattering Properties

    doi: 10.3390/bios16050292

    Figure Lengend Snippet: ( a , b ) Average fluorescence intensities of Cy3 at different concentrations on silver nanostructured surfaces and a glass slide; ( c ) fluorescence enhancement factor of the silver nanostructured surfaces relative to the glass slide.

    Article Snippet: Cy3 and Rhodamine 6G (R6G) were used as probe molecules and purchased from Macklin Biochemical Co., Ltd. (Shanghai, China).

    Techniques: Fluorescence