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anti yap  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti yap
    Anti Yap, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1491 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+yap/YAP+XP+Rabbit+mAb/pm42894734-264-38-40
    Average 98 stars, based on 1491 article reviews
    anti yap - by Bioz Stars, 2026-10
    98/100 stars

    Images

    Related Articles

    Magnetic Beads:

    Article Title: Inflammatory macrophages drive smooth muscle dedifferentiation via YAP signaling in murine deep vein thrombosis.
    Article Snippet: Cells were lysed in Pierce IP Lysis Buffer (Thermo Scientific, 87787) and coimmunoprecipitation experiments were performed using SureBeads magnetic beads (Biorad, 1614013) as per the manufacturer’s protocol. .. In brief, Protein A magnetic beads were washed in TBST, incubated with anti-YAP (14074, Cell Signaling Technology, 1:1000) or rabbit IgG isotype control (Thermo Scientific, 026102) for 30 minutes at room temperature, and then magnetized and washed three times with TBST. ..

    Incubation:

    Article Title: Inflammatory macrophages drive smooth muscle dedifferentiation via YAP signaling in murine deep vein thrombosis.
    Article Snippet: Cells were lysed in Pierce IP Lysis Buffer (Thermo Scientific, 87787) and coimmunoprecipitation experiments were performed using SureBeads magnetic beads (Biorad, 1614013) as per the manufacturer’s protocol. .. In brief, Protein A magnetic beads were washed in TBST, incubated with anti-YAP (14074, Cell Signaling Technology, 1:1000) or rabbit IgG isotype control (Thermo Scientific, 026102) for 30 minutes at room temperature, and then magnetized and washed three times with TBST. ..

    Article Title: Neuronal and Glial YAP/TAZ in the Spinal Cord Contribute to the Development of Bone Cancer Pain in Mice.
    Article Snippet: The treatment of bone cancer pain (BCP) remains a major clinical challenge, and the mechanisms underlying BCP remain poorly understood.. Here, we report that tumor cell implantation (TCI) led to nuclear accumulation of yes-associated protein (YAP) and transcriptional coactivator with PDZ (postsynaptic density protein 95, PSD95; discs large, Dlg; zonula occludens-1, ZO-1)-binding motif (TAZ) and up-regulation of their mRNA (messenger ribonucleic acid) expression in Vglut2+ excitatory neurons, microglia, and astrocytes in the spinal dorsal horn.. Pharmacological inhibition of YAP/TAZ or genetic knockout of YAP/TAZ in Vglut2+ excitatory neurons, microglia, or astrocytes significantly alleviates TCI-induced BCP.

    Article Title: Inflammatory macrophages drive smooth muscle dedifferentiation via YAP signaling in murine deep vein thrombosis.
    Article Snippet: .. The membranes were blocked with 5% skim milk, and incubated overnight at 4 °C with the following primary antibodies: anti-Phospho-YAP (Ser127) (13008, Cell Signaling Technology; 1:1000), anti-YAP (14074, Cell Signaling Technology, 1:1000), anti-PhosphoYAP (Ser397) (13619, Cell Signaling Technology; 1:1000), anti-SM22α (36090, Cell Signaling Technology; 1:1000), anti-MYH11 (ab133567, Abcam; 1:1000), anti-Pan-TEAD (13295, Cell Signaling Technology, 1:1000), anti-α-smooth muscle actin (19245, Cell Signaling Technology, 1:1000), anti-β-actin (A5441, Sigma-Aldrich, 1:5000), followed by HRP (horseradish peroxidase)-labeled secondary antibody (Jackson ImmunoResearch, 1:5000). .. Total RNA was extracted from cultured cells using PureLinkTM RNA Mini Kit (12183018A, ThermoFisher Scientific) according to manufacturer’s protocols.

    Article Title: Injectable mRNA-engineered short fibers deliver temporally coupled mechano-genetic signals to reprogram Schwann cell cytoskeleton for nerve repair.
    Article Snippet: .. Sections were blocked with 5% BSA and incubated with primary antibodies overnight at 4 ◦C: anti-c-Jun antibody (9165S, CST, Danvers, MA), anti-S100β (90393, CST, Danvers, MA), anti-GAP43 antibody (87287-1-RR, Proteintech, Wuhan, China), anti-CD31 antibody (3528S, CST, Danvers, MA), anti-YAP (14074T, CST, Danvers, MA) and anti-Tuj1 (5568S, CST, Danvers, MA), anti-Myelin Protein Zero antibody (57518S, CST, Danvers, MA, USA) and anti-p75NTR antibody (55014, proteintech, Wuhan, China). .. After incubation with Alexa Fluor-conjugated secondary antibodies (ab150077/ab150115, Abcam, Cambridge, UK), nuclei were counterstained with DAPI.

    Control:

    Article Title: Inflammatory macrophages drive smooth muscle dedifferentiation via YAP signaling in murine deep vein thrombosis.
    Article Snippet: Cells were lysed in Pierce IP Lysis Buffer (Thermo Scientific, 87787) and coimmunoprecipitation experiments were performed using SureBeads magnetic beads (Biorad, 1614013) as per the manufacturer’s protocol. .. In brief, Protein A magnetic beads were washed in TBST, incubated with anti-YAP (14074, Cell Signaling Technology, 1:1000) or rabbit IgG isotype control (Thermo Scientific, 026102) for 30 minutes at room temperature, and then magnetized and washed three times with TBST. ..

    Binding Assay:

    Article Title: Neuronal and Glial YAP/TAZ in the Spinal Cord Contribute to the Development of Bone Cancer Pain in Mice.
    Article Snippet: The treatment of bone cancer pain (BCP) remains a major clinical challenge, and the mechanisms underlying BCP remain poorly understood.. Here, we report that tumor cell implantation (TCI) led to nuclear accumulation of yes-associated protein (YAP) and transcriptional coactivator with PDZ (postsynaptic density protein 95, PSD95; discs large, Dlg; zonula occludens-1, ZO-1)-binding motif (TAZ) and up-regulation of their mRNA (messenger ribonucleic acid) expression in Vglut2+ excitatory neurons, microglia, and astrocytes in the spinal dorsal horn.. Pharmacological inhibition of YAP/TAZ or genetic knockout of YAP/TAZ in Vglut2+ excitatory neurons, microglia, or astrocytes significantly alleviates TCI-induced BCP.

    other:

    Article Title: Adaptable sliding hydrogels enable pericellular pocket formation while enhancing MSC chondrogenesis and survival in 3D
    Article Snippet: After PBS washing, samples were blocked for 30 min and then incubated overnight in primary antibody overnight at 4 °C at a 1:100 dilution (Abcam 34712, Abcam 34710, and Thermo Scientific 14-9771-82).

    Article Title: From disease model to therapeutic insight: An engineered hydrogel reveals the role of matrix viscous dissipation in intervertebral disc degeneration
    Article Snippet: Inhibitors in cell culture were used at the following concertation: 0.25 μM VP to inhibit YAP (MCE, China, CL 318952), 10 μM PF-573228 (MCE, China, HY-10461) to inhibit p-FAK, 1 μg ml −1 ITGB 1-blocking antibody (Abcam, NBP2-16974), VBIT-4 (MCE, China, HY-129122) to inhibit mitochondria damage and SN-011 (MCE, China, HY-145010) to inhibit STING.

    Immunofluorescence:

    Article Title: Integrin‐Binding Matricellular Protein Fibulin‐5 Maintains Epidermal Stem Cell Heterogeneity During Skin Aging
    Article Snippet: .. Immunofluorescence staining was performed as previously described (Xuan Ngo et al. ) using the following primary antibodies: rabbit anti‐YAP (1:100; Cell Signaling Technology, 4912S), mouse anti‐Ki‐67 (1:200; BD Bioscience, 14‐5698‐82), rabbit anti‐ASS1 (1:1000; Cell Signaling Technology, 05‐665), and guinea pig anti‐SLC1A3 (1:100; Frontier Institute, GLAST‐GP‐Af1000). ..

    Staining:

    Article Title: Integrin‐Binding Matricellular Protein Fibulin‐5 Maintains Epidermal Stem Cell Heterogeneity During Skin Aging
    Article Snippet: .. Immunofluorescence staining was performed as previously described (Xuan Ngo et al. ) using the following primary antibodies: rabbit anti‐YAP (1:100; Cell Signaling Technology, 4912S), mouse anti‐Ki‐67 (1:200; BD Bioscience, 14‐5698‐82), rabbit anti‐ASS1 (1:1000; Cell Signaling Technology, 05‐665), and guinea pig anti‐SLC1A3 (1:100; Frontier Institute, GLAST‐GP‐Af1000). ..



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    Q209R preferentially engages <t>FAK‐YAP</t> signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, <t>p‐4EBP1</t> <t>(Ser65),</t> and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .
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    SMFs amplify the response of orthodontic mechanical signaling pathways. (a) Representative immunofluorescence images of vinculin (green), F‐actin (purple), and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), with mechanical force only, and with mechanical force plus SMFs. Scale bar: 10 µm. (b) Cell area, (c) FA area per cell, and (d) cell shape index in PDLCs. Mean ± SD. n = 24. * p < 0.05, ** p < 0.01, **** p < 0.0001. (e) FAK: Focal Adhesion Kinase. It is a mechanotransducer that becomes activated upon orthodontic force, regulating downstream bone remodeling and inflammatory responses in PDLCs. Representative immunofluorescence images of FAK (red) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (f) Relative FAK integrated density per cell in PDLCs. Mean ± SD. n = 24. **** p < 0.0001. (g) Representative immunofluorescence images <t>of</t> <t>YAP/TAZ</t> (green) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (h) The nuclear‐cytoplasmic ratios of YAP/TAZ in PDLCs analyzed from the immunofluorescence images. Mean ± SD. n = 24. ** p < 0.01, *** p < 0.001, **** p < 0.0001.
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    Organoid characterization images. (A–C) H&E staining images, (D–F) immunofluorescence staining for TUJ1, <t>(G–I)</t> <t>YAP/TAZ</t> (green), (J–L) calretinin (green), (M‐O) FOXG1 (green), (P–S) TTR (green) markers with DAPI (nuclei‐blue) for the organoids at day 30 (scale bar 100 µm).
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    Image Search Results


    Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Journal: Pigment Cell & Melanoma Research

    Article Title: Allele‐Specific GNAQ Q209 Mutations Reveal Context‐Dependent Oncogenic Programs in Uveal Melanoma

    doi: 10.1111/pcmr.70121

    Figure Lengend Snippet: Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Article Snippet: Antibodies against GNAQ (CST, #14373, RRID:AB_2665457), BAP1 (Abcam, ab255611), Melan‐A (Abcam, ab210546, RRID:AB_2889292), ERK1/2 (CST, #4695, RRID:AB_390779), p‐ERK1/2 (Thr202/Tyr204) (CST, #4370, RRID:AB_2315112), FRA1 (Abcam, ab252421, RRID:AB_2904513), AKT (CST, #4691, RRID:AB_915783), p‐AKT (Ser473) (CST, #4060, RRID:AB_2315049), p‐FAK (Tyr397) (CST, #8556, RRID:AB_10891442), FAK (CST, #3285, RRID:AB_2269034), 4E‐BP1 (CST, #9452, RRID:AB_331692), p‐4E‐BP1 (Ser65; CST, #9451, RRID:AB_330947), YAP (CST, #4912, RRID:AB_2218911), and p‐YAP (Ser127) (CST, #4911, RRID:AB_2218913) were used at 1:1000 as indicated.

    Techniques: Western Blot, Analysis, Expressing, Control, Derivative Assay, Transplantation Assay

    Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Journal: Pigment Cell & Melanoma Research

    Article Title: Allele‐Specific GNAQ Q209 Mutations Reveal Context‐Dependent Oncogenic Programs in Uveal Melanoma

    doi: 10.1111/pcmr.70121

    Figure Lengend Snippet: Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Article Snippet: Antibodies against GNAQ (CST, #14373, RRID:AB_2665457), BAP1 (Abcam, ab255611), Melan‐A (Abcam, ab210546, RRID:AB_2889292), ERK1/2 (CST, #4695, RRID:AB_390779), p‐ERK1/2 (Thr202/Tyr204) (CST, #4370, RRID:AB_2315112), FRA1 (Abcam, ab252421, RRID:AB_2904513), AKT (CST, #4691, RRID:AB_915783), p‐AKT (Ser473) (CST, #4060, RRID:AB_2315049), p‐FAK (Tyr397) (CST, #8556, RRID:AB_10891442), FAK (CST, #3285, RRID:AB_2269034), 4E‐BP1 (CST, #9452, RRID:AB_331692), p‐4E‐BP1 (Ser65; CST, #9451, RRID:AB_330947), YAP (CST, #4912, RRID:AB_2218911), and p‐YAP (Ser127) (CST, #4911, RRID:AB_2218913) were used at 1:1000 as indicated.

    Techniques: Western Blot, Analysis, Expressing, Control, Derivative Assay, Transplantation Assay

    SMFs amplify the response of orthodontic mechanical signaling pathways. (a) Representative immunofluorescence images of vinculin (green), F‐actin (purple), and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), with mechanical force only, and with mechanical force plus SMFs. Scale bar: 10 µm. (b) Cell area, (c) FA area per cell, and (d) cell shape index in PDLCs. Mean ± SD. n = 24. * p < 0.05, ** p < 0.01, **** p < 0.0001. (e) FAK: Focal Adhesion Kinase. It is a mechanotransducer that becomes activated upon orthodontic force, regulating downstream bone remodeling and inflammatory responses in PDLCs. Representative immunofluorescence images of FAK (red) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (f) Relative FAK integrated density per cell in PDLCs. Mean ± SD. n = 24. **** p < 0.0001. (g) Representative immunofluorescence images of YAP/TAZ (green) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (h) The nuclear‐cytoplasmic ratios of YAP/TAZ in PDLCs analyzed from the immunofluorescence images. Mean ± SD. n = 24. ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Journal: Advanced Science

    Article Title: Arrayed Magnetic Accelerator Synergistically Enhances Orthodontic Tooth Movement via Microtubule Assembly‐Mediated Periodontal Remodeling

    doi: 10.1002/advs.77447

    Figure Lengend Snippet: SMFs amplify the response of orthodontic mechanical signaling pathways. (a) Representative immunofluorescence images of vinculin (green), F‐actin (purple), and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), with mechanical force only, and with mechanical force plus SMFs. Scale bar: 10 µm. (b) Cell area, (c) FA area per cell, and (d) cell shape index in PDLCs. Mean ± SD. n = 24. * p < 0.05, ** p < 0.01, **** p < 0.0001. (e) FAK: Focal Adhesion Kinase. It is a mechanotransducer that becomes activated upon orthodontic force, regulating downstream bone remodeling and inflammatory responses in PDLCs. Representative immunofluorescence images of FAK (red) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (f) Relative FAK integrated density per cell in PDLCs. Mean ± SD. n = 24. **** p < 0.0001. (g) Representative immunofluorescence images of YAP/TAZ (green) and nuclei (blue) in PDLCs under three conditions: control (without mechanical force and without SMFs), mechanical force only, and mechanical force plus SMFs. Scale bar: 10 µm. (h) The nuclear‐cytoplasmic ratios of YAP/TAZ in PDLCs analyzed from the immunofluorescence images. Mean ± SD. n = 24. ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Article Snippet: PDLCs were respectively incubated with the primary antibody for Vinculin (Proteintech, 26520‐1‐Ap, 1:300), FAK (Proteintech, 12636‐1‐AP, 1:400), YAP/TAZ (Proteintech, 13584‐1‐Ap, 1:200), α‐Tubulin (Abclonal, AC012, 1:200) and Integrin‐β1 (Abclonal, A23497, 1:200).

    Techniques: Protein-Protein interactions, Immunofluorescence, Control

    Organoid characterization images. (A–C) H&E staining images, (D–F) immunofluorescence staining for TUJ1, (G–I) YAP/TAZ (green), (J–L) calretinin (green), (M‐O) FOXG1 (green), (P–S) TTR (green) markers with DAPI (nuclei‐blue) for the organoids at day 30 (scale bar 100 µm).

    Journal: Developmental Neurobiology

    Article Title: Molecular and Proteomic Profiling of Human Cerebral Organoid‑Derived Small Extracellular Vesicles

    doi: 10.1002/dneu.70062

    Figure Lengend Snippet: Organoid characterization images. (A–C) H&E staining images, (D–F) immunofluorescence staining for TUJ1, (G–I) YAP/TAZ (green), (J–L) calretinin (green), (M‐O) FOXG1 (green), (P–S) TTR (green) markers with DAPI (nuclei‐blue) for the organoids at day 30 (scale bar 100 µm).

    Article Snippet: Subsequently, primary antibodies TUJ1 (R&D Systems, MAB1195), Calretinin (Proteintech, 12278‐1‐AP), FOXG1 (ThermoFisher Scientific, PA526794 ), TTR (Proteintech, 11891‐1‐AP), and YAP/TAZ (CST, 8418S) were added and incubated overnight at 4°C.

    Techniques: Staining, Immunofluorescence, Organoids