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polyclonal mcherry genetex 1:2000 antibody  (GeneTex)

 
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    Structured Review

    GeneTex polyclonal mcherry genetex 1:2000 antibody
    TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and <t>NPY-mCherry</t> (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .
    Polyclonal Mcherry Genetex 1:2000 Antibody, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/polyclonal+mcherry+genetex+1%3A2000+antibody/pmc07331729-253-30-32?v=GeneTex
    Average 90 stars, based on 1 article reviews
    polyclonal mcherry genetex 1:2000 antibody - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Tetanus insensitive VAMP2 differentially restores synaptic and dense core vesicle fusion in tetanus neurotoxin treated neurons"

    Article Title: Tetanus insensitive VAMP2 differentially restores synaptic and dense core vesicle fusion in tetanus neurotoxin treated neurons

    Journal: Scientific Reports

    doi: 10.1038/s41598-020-67988-2

    TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and NPY-mCherry (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .
    Figure Legend Snippet: TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and NPY-mCherry (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .

    Techniques Used: Infection



    Similar Products

    polyclonal mcherry genetex 1:2000 antibody  (GeneTex)
    90
    GeneTex polyclonal mcherry genetex 1:2000 antibody
    TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and <t>NPY-mCherry</t> (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .
    Polyclonal Mcherry Genetex 1:2000 Antibody, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/polyclonal+mcherry+genetex+1%3A2000+antibody/pmc07331729-253-30-32?v=GeneTex
    Average 90 stars, based on 1 article reviews
    polyclonal mcherry genetex 1:2000 antibody - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and NPY-mCherry (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .

    Journal: Scientific Reports

    Article Title: Tetanus insensitive VAMP2 differentially restores synaptic and dense core vesicle fusion in tetanus neurotoxin treated neurons

    doi: 10.1038/s41598-020-67988-2

    Figure Lengend Snippet: TI-VAMP1 and TI-VAMP2 co-travel with DCVs. ( A ) Representative kymographs of neurons co-infected (at DIV 4–6) with TI-VAMP1 and NPY-mCherry (left), or TI-VAMP2 and NPY-mCherry (right), imaged at DIV 11–13. VAMP kymographs in green, NPY kymographs in magenta. The bottom panels are graphic representations of the kymographs to show the quantification of the tracks: VAMP only (green), NPY only (magenta) or co-trafficking/localization (black). ( B ) Percentage moving (diagonal line in kymograph) TI-VAMP1 (n = 16, N = 2) TI-VAMP2 (n = 14, N = 2), and NPY (n = 30, N = 2) puncta. 1-way ANOVA with post-hoc Tukey’s test: VAMP2 vs VAMP1/NPY: p = 0.001 (***). ( C ) Percentage of moving NPY puncta with VAMP1 and VAMP2, and moving VAMP1 and VAMP2 puncta with NPY. 1-way ANOVA: p = 0.48 non-significant (ns). Bars represent mean + SEM. Detailed statistics are shown in Supplementary Table .

    Article Snippet: Primary antibodies used were: polyclonal MAP2 (Abcam 1:1,000), monoclonal VAMP2 (Sysy, 1:2000), polyclonal GFP (bioconnect, 1:1,000), polyclonal SCG2 (Biodesign International, 1:500), monoclonal BDNF (DSHB, 1:4), polyclonal synaptophysin 1 (SySy, 1:1,000) polyclonal mCherry (GeneTex, 1:2000), polyclonal HA-tag (Abcam, 1:500).

    Techniques: Infection