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anti human rab7 abs  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti human rab7 abs
    A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein <t>GFP-Rab7</t> on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).
    Anti Human Rab7 Abs, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+human+rab7+abs/med_rxiv__64898__2026__04__03__26349989-68-25-28
    Average 86 stars, based on 1 article reviews
    anti human rab7 abs - by Bioz Stars, 2026-09
    86/100 stars

    Images

    1) Product Images from "Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation"

    Article Title: Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation

    Journal: medRxiv

    doi: 10.64898/2026.04.03.26349989

    A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein GFP-Rab7 on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).
    Figure Legend Snippet: A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein GFP-Rab7 on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).

    Techniques Used: Marker, Comparison, MANN-WHITNEY, Expressing, Fluorescence

    Related Articles

    Staining:

    Article Title: Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation
    Article Snippet: .. Cells were then saturated using TBS-Tween 0.01% supplemented with 3% goat serum, and stained with a primary anti-human WDR91 Ab (Abcam) and anti-human EEA1 or anti-human Rab7 Abs (Cell Signaling Technologies) and a secondary goat anti-mouse/rabbit IgG mAb coupled to AF488 or AF687 (Thermo Fisher Scientific). .. Nuclei were counterstained with SYTOX Orange (Invitrogen), and coverslips were mounted using ProLong Diamond Antifade Mountant (Molecular Probes).



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    anti human rab7 abs  (Cell Signaling Technology Inc)
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    Cell Signaling Technology Inc anti human rab7 abs
    A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein <t>GFP-Rab7</t> on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).
    Anti Human Rab7 Abs, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+human+rab7+abs/med_rxiv__64898__2026__04__03__26349989-68-25-28
    Average 86 stars, based on 1 article reviews
    anti human rab7 abs - by Bioz Stars, 2026-09
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein GFP-Rab7 on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).

    Journal: medRxiv

    Article Title: Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation

    doi: 10.64898/2026.04.03.26349989

    Figure Lengend Snippet: A. Time-lapse recording of dynamic changes of the early endosomal marker 2×FYVE-mCherry and the late endosomal protein GFP-Rab7 on endosomes in transduced HEK193 cells (left) and duration of the overlap of 2×FYVE and Rab7 on endosomes (right; one-way ANOVA with Kruskal-Wallis multiple comparison test, ** p<0.01, **** p<10 - ; at least 10 endosomes per cell line were analyzed). B. Colocalization of endogenous EEA1 with Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; Mann-Whitney test, *** p<10 - ; at least 30 independent cells per cell line were analyzed). C. EEA1 and Rab7 protein expression in transduced HEK293 cells, representative blot of three independent experiments. Individual fluorescence channels were analyzed separately due to distinct background signal. D. Colocalization of WDR91 with endogenous EEA1 or Rab7 in WDR91 WT and WDR91 Y15N cells: representative confocal images (left) and assessment of Pearson’s coefficient (right; 2-way ANOVA with Sidak multiple comparison test, *** p<10 -3 , **** p<10 -4 ; at least 30 independent cells per cell line were analyzed).

    Article Snippet: Cells were then saturated using TBS-Tween 0.01% supplemented with 3% goat serum, and stained with a primary anti-human WDR91 Ab (Abcam) and anti-human EEA1 or anti-human Rab7 Abs (Cell Signaling Technologies) and a secondary goat anti-mouse/rabbit IgG mAb coupled to AF488 or AF687 (Thermo Fisher Scientific).

    Techniques: Marker, Comparison, MANN-WHITNEY, Expressing, Fluorescence