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pmlc  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc pmlc
    ( A,B ) Representative immunofluorescence images <t>of</t> <t>paxillin</t> and F-actin (phalloidin) ( A ), and <t>pMLC</t> and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.
    Pmlc, 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/pmlc/pmc13068432-322-16-17
    Average 86 stars, based on 1 article reviews
    pmlc - by Bioz Stars, 2026-11
    86/100 stars

    Images

    1) Product Images from "GTPase-activating protein DLC1 spatio-temporally regulates Rho signaling"

    Article Title: GTPase-activating protein DLC1 spatio-temporally regulates Rho signaling

    Journal: eLife

    doi: 10.7554/eLife.90305

    ( A,B ) Representative immunofluorescence images of paxillin and F-actin (phalloidin) ( A ), and pMLC and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.
    Figure Legend Snippet: ( A,B ) Representative immunofluorescence images of paxillin and F-actin (phalloidin) ( A ), and pMLC and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.

    Techniques Used: Immunofluorescence

    Related Articles

    other:

    Article Title: A Mechanotransduction-Aware Strategy for Enhancing MSC Potency via 3D Culture and Localized Delivery
    Article Snippet: Phalloidin-TRITC was purchased from Invitrogen (USA).

    Staining:

    Article Title: Inflammasomes and DNA Damage Orchestrate Divergent Pyroptotic Fates in Neutrophils
    Article Snippet: .. Cells were permeabilized with 0.1% Triton X, blocked with 2% BSA, and stained overnight with primary antibodies as follows-8-OHdG (1:1000) (Obtained from Merck), IL-1β (1:100) (Invitrogen) or pMLC (1:100) (Myosin light chain; Cell Signaling Technology, Boston, MA) overnight at 4°C. .. Cells were then washed and stained with secondary antibody anti-goat Alexa fluor 488 or anti-rabbit Alexa fluor 488 for 2 h at RT (1:500, Invitrogen) and mounted in DAPI-containing media (Invitrogen) ( ).

    Blocking Assay:

    Article Title: Patterns of Mitochondrial ATP Predict Tissue Folding
    Article Snippet: .. After blocking, samples were incubated in blocking buffer containing primary antibodies against Tom20 (1:100; D8T4N, rabbit mAb; Cell Signaling 42406S), E-cadherin (1:500; clone 36, mouse mAb; BD 610182), or pMLC (1:50; Ser19, mouse mAb; Cell Signaling 3675S) for 48 hours at 4°C. ..

    Article Title: Rho kinase and RND3 regulate the direct effect of estradiol-17β on oviductal tonus.
    Article Snippet: Briefly, the lysates from oviductal isthmic smooth reproduction@bioscientifica.com Manuscript submitted for review to Reproduction D ow nloaded from https://academ ic.oup.com /reproduction/advance-article/doi/10.1093/reprod/xaag004/8439658 by guest on 27 January 2026 8 128 muscle tissues (25 μg/lane) were prepared, separated using SDS-PAGE (7%–13%), and 129 transferred to PVDF membranes. .. After blocking, the membranes were incubated with antibodies 130 against RhoA (sc-418, Santa Cruz Biotechnology, Santa Cruz, USA, RRID:AB_628218), ROCK 131 I (sc-17794, Santa Cruz Biotechnology, RRID:AB_628223), ROCK II (sc-398519, Santa Cruz 132 Biotechnology), RND1 (A06347, Boster Biological Technology, Wuhan, China), RND2 (13844- 133 1-AP, Proteintech, Wuhan, China, RRID:AB_2181817), RND3 (66228-1-lg, Proteintech), 134 MYPT1 (2634, Cell Signaling Technology, Massachusetts, USA, RRID:AB_915965), pMYPT1 135 (Thr696, 5163, Cell Signaling Technology, RRID:AB_10691830), pMYPT1 (Thr853, 4563, Cell 136 Signaling Technology, RRID:AB_1031185), MLC (8505, Cell Signaling Technology, 137 RRID:AB_2728760), pMLC (Thr18/Ser19, 3674, Cell Signaling Technology, 138 RRID:AB_2147464) or GAPDH (NB300-221SS, Novus Biologicals, Briarwood Avenue, USA, 139 RRID:AB_790028) diluted with Can Get Signal Solution 1 (NKB-201, TOYOBO) overnight at 140 4°C or for 2 h at room temperature. .. After washing with TBS-T, HRP-linked sheep anti-mouse 141 IgG (NA931, Cytiva, RRID:AB_772210), HRP-linked donkey anti-rabbit IgG (NA934, Cytiva, 142 RRID: AB_772206), or HRP-linked goat anti-mouse IgM (ab97230, Abcam, Cambridge, UK, 143 RRID:AB_10688258) diluted with Can Get Signal Solution 2 (NKB-301, TOYOBO) were 144 incubated to the membranes for 1 h at room temperature.

    Incubation:

    Article Title: Patterns of Mitochondrial ATP Predict Tissue Folding
    Article Snippet: .. After blocking, samples were incubated in blocking buffer containing primary antibodies against Tom20 (1:100; D8T4N, rabbit mAb; Cell Signaling 42406S), E-cadherin (1:500; clone 36, mouse mAb; BD 610182), or pMLC (1:50; Ser19, mouse mAb; Cell Signaling 3675S) for 48 hours at 4°C. ..

    Article Title: Rho kinase and RND3 regulate the direct effect of estradiol-17β on oviductal tonus.
    Article Snippet: Briefly, the lysates from oviductal isthmic smooth reproduction@bioscientifica.com Manuscript submitted for review to Reproduction D ow nloaded from https://academ ic.oup.com /reproduction/advance-article/doi/10.1093/reprod/xaag004/8439658 by guest on 27 January 2026 8 128 muscle tissues (25 μg/lane) were prepared, separated using SDS-PAGE (7%–13%), and 129 transferred to PVDF membranes. .. After blocking, the membranes were incubated with antibodies 130 against RhoA (sc-418, Santa Cruz Biotechnology, Santa Cruz, USA, RRID:AB_628218), ROCK 131 I (sc-17794, Santa Cruz Biotechnology, RRID:AB_628223), ROCK II (sc-398519, Santa Cruz 132 Biotechnology), RND1 (A06347, Boster Biological Technology, Wuhan, China), RND2 (13844- 133 1-AP, Proteintech, Wuhan, China, RRID:AB_2181817), RND3 (66228-1-lg, Proteintech), 134 MYPT1 (2634, Cell Signaling Technology, Massachusetts, USA, RRID:AB_915965), pMYPT1 135 (Thr696, 5163, Cell Signaling Technology, RRID:AB_10691830), pMYPT1 (Thr853, 4563, Cell 136 Signaling Technology, RRID:AB_1031185), MLC (8505, Cell Signaling Technology, 137 RRID:AB_2728760), pMLC (Thr18/Ser19, 3674, Cell Signaling Technology, 138 RRID:AB_2147464) or GAPDH (NB300-221SS, Novus Biologicals, Briarwood Avenue, USA, 139 RRID:AB_790028) diluted with Can Get Signal Solution 1 (NKB-201, TOYOBO) overnight at 140 4°C or for 2 h at room temperature. .. After washing with TBS-T, HRP-linked sheep anti-mouse 141 IgG (NA931, Cytiva, RRID:AB_772210), HRP-linked donkey anti-rabbit IgG (NA934, Cytiva, 142 RRID: AB_772206), or HRP-linked goat anti-mouse IgM (ab97230, Abcam, Cambridge, UK, 143 RRID:AB_10688258) diluted with Can Get Signal Solution 2 (NKB-301, TOYOBO) were 144 incubated to the membranes for 1 h at room temperature.

    Article Title: GTPase-activating protein DLC1 spatio-temporally regulates Rho signaling
    Article Snippet: .. Cells were incubated overnight with the primary antibody 1:250 dilution for paxillin (Abcam ab32084), 1:50 for pMLC (Cell Signaling Antibody #3671). ..



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    ( A,B ) Representative immunofluorescence images <t>of</t> <t>paxillin</t> and F-actin (phalloidin) ( A ), and <t>pMLC</t> and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.
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    Image Search Results


    ( A,B ) Representative immunofluorescence images of paxillin and F-actin (phalloidin) ( A ), and pMLC and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.

    Journal: eLife

    Article Title: GTPase-activating protein DLC1 spatio-temporally regulates Rho signaling

    doi: 10.7554/eLife.90305

    Figure Lengend Snippet: ( A,B ) Representative immunofluorescence images of paxillin and F-actin (phalloidin) ( A ), and pMLC and F-actin (phalloidin) ( B ) immunostains are shown in inverted black and white (ibw) contrast as well as color composites (DAPI signal also included). Scale bar = 10 µm. ( C ) Compared to WT cells (n=243), lamella size is significantly increased in DLC1 KD cells (n=290, p-adjusted<0.001) and DLC1 KO cells (n=242, p-adjusted<0.001), while DLC1 rescue cells (n=57) show significantly lower lamella sizes than both WT (p-adjusted=0.0098) and KO cells (p-adjusted<0.001). ( D ) DLC1 KD cells (n=290) display a significant increase in the total area of focal adhesions per cell (p-adjusted<0.001) compared to WT cells (n=243), while DLC1 KO cells (n=242) do not show a significant difference (p-adjusted=0.09). Rescue cells show a significant decrease in the total area of focal adhesions (p-adjusted<0.001). ANOVA plus Tukey’s honestly significant difference test.

    Article Snippet: Cells were incubated overnight with the primary antibody 1:250 dilution for paxillin (Abcam ab32084), 1:50 for pMLC (Cell Signaling Antibody #3671).

    Techniques: Immunofluorescence