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rab11a wild-type (rab11a)  (Agilent technologies)


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    Agilent technologies rab11a wild-type (rab11a)
    Rab11a Wild Type (Rab11a), supplied by Agilent technologies, 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/rab11a+wild-type+(rab11a)/pmc01995710-188-1-21
    Average 90 stars, based on 1 article reviews
    rab11a wild-type (rab11a) - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Dominant Negative Mutation:

    Article Title: Exocyst Requirement for Endocytic Traffic Directed Toward the Apical and Basolateral Poles of Polarized MDCK Cells
    Article Snippet: For two-hybrid analysis Rab11a wild-type (Rab11a), dominant negative Rab11a-S25N (Rab11aSN), and dominant active Rab11a-S20V (Rab11aSV) were subcloned into the pBDGAL-Cam vector (Stratagene, La Jolla, CA) using standard DNA technologies.

    Plasmid Preparation:

    Article Title: Exocyst Requirement for Endocytic Traffic Directed Toward the Apical and Basolateral Poles of Polarized MDCK Cells
    Article Snippet: For two-hybrid analysis Rab11a wild-type (Rab11a), dominant negative Rab11a-S25N (Rab11aSN), and dominant active Rab11a-S20V (Rab11aSV) were subcloned into the pBDGAL-Cam vector (Stratagene, La Jolla, CA) using standard DNA technologies.



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    (A) Mammary gland sections stained for E-cadherin and PAR3 or aPKC. Arrows indicate cytoplasmic accumulation and impaired localization of PAR3 and aPKC to the apical surface; asterisks indicate small lumens. (B) Mammary gland sections stained for keratin 5 (K5) and GM130. (C) Percentage of LCs showing ribbon-like and fragmented localization of GM130 (control: n = 4 mice; mutant: n = 4 mice). (D) Mammary gland sections stained for HTT 4C8 and PAR3 or aPKC. (E) <t>HTT/PAR3/PAR6/aPKC/RAB11A</t> complexes were immunoprecipitated from MCF-10A cells. Mouse IgG (mIgG) was used as a negative control. The immunoprecipitates (IP) were analyzed by western blotting. All scale bars, 10 μm. Error bars, SEM. *** p <0.001. Complete statistical analyses with number of measures are detailed in .
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    rab11a wild-type (rab11a)  (Agilent technologies)
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    (A) Mammary gland sections stained for E-cadherin and PAR3 or aPKC. Arrows indicate cytoplasmic accumulation and impaired localization of PAR3 and aPKC to the apical surface; asterisks indicate small lumens. (B) Mammary gland sections stained for keratin 5 (K5) and GM130. (C) Percentage of LCs showing ribbon-like and fragmented localization of GM130 (control: n = 4 mice; mutant: n = 4 mice). (D) Mammary gland sections stained for HTT 4C8 and PAR3 or aPKC. (E) <t>HTT/PAR3/PAR6/aPKC/RAB11A</t> complexes were immunoprecipitated from MCF-10A cells. Mouse IgG (mIgG) was used as a negative control. The immunoprecipitates (IP) were analyzed by western blotting. All scale bars, 10 μm. Error bars, SEM. *** p <0.001. Complete statistical analyses with number of measures are detailed in .
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    Image Search Results


    (A) Mammary gland sections stained for E-cadherin and PAR3 or aPKC. Arrows indicate cytoplasmic accumulation and impaired localization of PAR3 and aPKC to the apical surface; asterisks indicate small lumens. (B) Mammary gland sections stained for keratin 5 (K5) and GM130. (C) Percentage of LCs showing ribbon-like and fragmented localization of GM130 (control: n = 4 mice; mutant: n = 4 mice). (D) Mammary gland sections stained for HTT 4C8 and PAR3 or aPKC. (E) HTT/PAR3/PAR6/aPKC/RAB11A complexes were immunoprecipitated from MCF-10A cells. Mouse IgG (mIgG) was used as a negative control. The immunoprecipitates (IP) were analyzed by western blotting. All scale bars, 10 μm. Error bars, SEM. *** p <0.001. Complete statistical analyses with number of measures are detailed in .

    Journal: PLoS Biology

    Article Title: Huntingtin Is Required for Epithelial Polarity through RAB11A-Mediated Apical Trafficking of PAR3-aPKC

    doi: 10.1371/journal.pbio.1002142

    Figure Lengend Snippet: (A) Mammary gland sections stained for E-cadherin and PAR3 or aPKC. Arrows indicate cytoplasmic accumulation and impaired localization of PAR3 and aPKC to the apical surface; asterisks indicate small lumens. (B) Mammary gland sections stained for keratin 5 (K5) and GM130. (C) Percentage of LCs showing ribbon-like and fragmented localization of GM130 (control: n = 4 mice; mutant: n = 4 mice). (D) Mammary gland sections stained for HTT 4C8 and PAR3 or aPKC. (E) HTT/PAR3/PAR6/aPKC/RAB11A complexes were immunoprecipitated from MCF-10A cells. Mouse IgG (mIgG) was used as a negative control. The immunoprecipitates (IP) were analyzed by western blotting. All scale bars, 10 μm. Error bars, SEM. *** p <0.001. Complete statistical analyses with number of measures are detailed in .

    Article Snippet: GFP-RAB11A wild-type (WT), dominant-negative (S25N), and constitutively active (Q70L) (referred to herein as RAB11A WT , RAB11A S25N and RAB11A Q70L , respectively) were obtained from B. Goud (Institut Curie, France).

    Techniques: Staining, Control, Mutagenesis, Immunoprecipitation, Negative Control, Western Blot

    (A) Mammary gland section stained for HTT 4C8 and RAB11A. (B) Mammary gland section stained for E-cadherin and RAB11A. (C) Twenty-four–hour and four-day MDCK 3-D cultures stained for HTT 4C8 and RAB11A. Colocalization of HTT and RAB11A is displayed in yellow (merge). (D) Twenty-four–hour and four-day MDCK 3-D cultures stained for RAB11A. HTTFL is tagged with mCherry and fluorescence is displayed in magenta and the colocalization of RAB11A and HTTFL appears in white. (E) Twenty-four–hour and four-day MDCK 3-D cultures transfected with RAB11A WT , RAB11A Q70L or RAB11A S22N , stained for PAR3. RAB11 is tagged with GFP and fluorescence is displayed in magenta. The colocalization of aPKC and RAB11A appears in white. (F) Representative line-scan analysis (relative fluorescence intensity; at least 20 cells were analyzed per condition). (G) Percentage of acini with normal lumen. (H) Quantification of acini size. (G and H) Control+RAB11A WT : n = 59 acini, Control+RAB11A Q70L : n = 54 acini, Control+RAB11A S22N : n = 66 acini, shHTT2+RAB11A WT : n = 60 acini, shHTT2+RAB11A Q70L : n = 72 acini, shHTT2+RAB11A S22N : n = 93 acini. (I) FM64-4 4-day MDCK 3-D structures were video recorded. Maximum intensity and z projections are shown. All scale bars, 10 μm. Error bars, SEM. ** p <0.01; *** p <0.001. Complete statistical analyses with number of measures are detailed in .

    Journal: PLoS Biology

    Article Title: Huntingtin Is Required for Epithelial Polarity through RAB11A-Mediated Apical Trafficking of PAR3-aPKC

    doi: 10.1371/journal.pbio.1002142

    Figure Lengend Snippet: (A) Mammary gland section stained for HTT 4C8 and RAB11A. (B) Mammary gland section stained for E-cadherin and RAB11A. (C) Twenty-four–hour and four-day MDCK 3-D cultures stained for HTT 4C8 and RAB11A. Colocalization of HTT and RAB11A is displayed in yellow (merge). (D) Twenty-four–hour and four-day MDCK 3-D cultures stained for RAB11A. HTTFL is tagged with mCherry and fluorescence is displayed in magenta and the colocalization of RAB11A and HTTFL appears in white. (E) Twenty-four–hour and four-day MDCK 3-D cultures transfected with RAB11A WT , RAB11A Q70L or RAB11A S22N , stained for PAR3. RAB11 is tagged with GFP and fluorescence is displayed in magenta. The colocalization of aPKC and RAB11A appears in white. (F) Representative line-scan analysis (relative fluorescence intensity; at least 20 cells were analyzed per condition). (G) Percentage of acini with normal lumen. (H) Quantification of acini size. (G and H) Control+RAB11A WT : n = 59 acini, Control+RAB11A Q70L : n = 54 acini, Control+RAB11A S22N : n = 66 acini, shHTT2+RAB11A WT : n = 60 acini, shHTT2+RAB11A Q70L : n = 72 acini, shHTT2+RAB11A S22N : n = 93 acini. (I) FM64-4 4-day MDCK 3-D structures were video recorded. Maximum intensity and z projections are shown. All scale bars, 10 μm. Error bars, SEM. ** p <0.01; *** p <0.001. Complete statistical analyses with number of measures are detailed in .

    Article Snippet: GFP-RAB11A wild-type (WT), dominant-negative (S25N), and constitutively active (Q70L) (referred to herein as RAB11A WT , RAB11A S25N and RAB11A Q70L , respectively) were obtained from B. Goud (Institut Curie, France).

    Techniques: Staining, Fluorescence, Transfection, Control

    During epithelial morphogenesis, HTT modulates the activation of RAB11A (1). HTT-RAB11A forms a complex with PAR3-aPKC, which may be recruited to HTT-kinesin 1 apical vesicles (2). HTT coordinates apical recycling of PAR3-aPKC vesicles (3). PAR3-aPKC accumulation at the pre-apical patches (PAP) (4) triggers the expansion of the apical membrane, leading to the formation of a central lumen (5).

    Journal: PLoS Biology

    Article Title: Huntingtin Is Required for Epithelial Polarity through RAB11A-Mediated Apical Trafficking of PAR3-aPKC

    doi: 10.1371/journal.pbio.1002142

    Figure Lengend Snippet: During epithelial morphogenesis, HTT modulates the activation of RAB11A (1). HTT-RAB11A forms a complex with PAR3-aPKC, which may be recruited to HTT-kinesin 1 apical vesicles (2). HTT coordinates apical recycling of PAR3-aPKC vesicles (3). PAR3-aPKC accumulation at the pre-apical patches (PAP) (4) triggers the expansion of the apical membrane, leading to the formation of a central lumen (5).

    Article Snippet: GFP-RAB11A wild-type (WT), dominant-negative (S25N), and constitutively active (Q70L) (referred to herein as RAB11A WT , RAB11A S25N and RAB11A Q70L , respectively) were obtained from B. Goud (Institut Curie, France).

    Techniques: Activation Assay, Membrane