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Proteintech α sma
Efficacy of GelMA MAVP MPs in promoting nerve end interface self-resolution. ( A ) Schematic of the peripheral sciatic nerve ligation (p-SNL) model with four experimental groups (i.e., MAVP, VAN, vehicle, and control) ( B ) Immunofluorescence (IF) staining of p-VEGFR2 and YAP (indicating mechanotransduction signaling). ( C ) The positive area percentage of p-VEGFR2 (n = 6). ( D ) Percentage of YAP in nuclear/cytoplasm (n = 6). ( E ) IF staining of proliferation signal (Ki-67) and vessel signal (CD31) for p-SNL animal. ( F ) Quantification of Ki-67/CD31 co-localization area percentage (n = 6). ( G ) IF co-staining of Ki-67 and macrophage marker F4/80. ( H ) Quantification of Ki-67/F4/80 co-localization area percentage (n = 6). ( I ) IF staining of scar <t>marker</t> <t>α-SMA.</t> ( J ) Quantification <t>of</t> <t>α-SMA-positive</t> area percentage (n = 6). Mean values are shown and error bars represent ± s.d., as analyzed by one-way ANOVA followed by the Tukey-Kramer test in ( C , D , F , H and J ). Biological replicates were used for all experiments. ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
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1) Product Images from "Targeting VEGFR2 inhibition within a spatially-confined conduit promotes nerve self-resolution and alleviates mechanical allodynia"

Article Title: Targeting VEGFR2 inhibition within a spatially-confined conduit promotes nerve self-resolution and alleviates mechanical allodynia

Journal: Bioactive Materials

doi: 10.1016/j.bioactmat.2026.03.009

Efficacy of GelMA MAVP MPs in promoting nerve end interface self-resolution. ( A ) Schematic of the peripheral sciatic nerve ligation (p-SNL) model with four experimental groups (i.e., MAVP, VAN, vehicle, and control) ( B ) Immunofluorescence (IF) staining of p-VEGFR2 and YAP (indicating mechanotransduction signaling). ( C ) The positive area percentage of p-VEGFR2 (n = 6). ( D ) Percentage of YAP in nuclear/cytoplasm (n = 6). ( E ) IF staining of proliferation signal (Ki-67) and vessel signal (CD31) for p-SNL animal. ( F ) Quantification of Ki-67/CD31 co-localization area percentage (n = 6). ( G ) IF co-staining of Ki-67 and macrophage marker F4/80. ( H ) Quantification of Ki-67/F4/80 co-localization area percentage (n = 6). ( I ) IF staining of scar marker α-SMA. ( J ) Quantification of α-SMA-positive area percentage (n = 6). Mean values are shown and error bars represent ± s.d., as analyzed by one-way ANOVA followed by the Tukey-Kramer test in ( C , D , F , H and J ). Biological replicates were used for all experiments. ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
Figure Legend Snippet: Efficacy of GelMA MAVP MPs in promoting nerve end interface self-resolution. ( A ) Schematic of the peripheral sciatic nerve ligation (p-SNL) model with four experimental groups (i.e., MAVP, VAN, vehicle, and control) ( B ) Immunofluorescence (IF) staining of p-VEGFR2 and YAP (indicating mechanotransduction signaling). ( C ) The positive area percentage of p-VEGFR2 (n = 6). ( D ) Percentage of YAP in nuclear/cytoplasm (n = 6). ( E ) IF staining of proliferation signal (Ki-67) and vessel signal (CD31) for p-SNL animal. ( F ) Quantification of Ki-67/CD31 co-localization area percentage (n = 6). ( G ) IF co-staining of Ki-67 and macrophage marker F4/80. ( H ) Quantification of Ki-67/F4/80 co-localization area percentage (n = 6). ( I ) IF staining of scar marker α-SMA. ( J ) Quantification of α-SMA-positive area percentage (n = 6). Mean values are shown and error bars represent ± s.d., as analyzed by one-way ANOVA followed by the Tukey-Kramer test in ( C , D , F , H and J ). Biological replicates were used for all experiments. ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

Techniques Used: Ligation, Control, Immunofluorescence, Staining, Marker

Expression of pain signal proteins in peripheral nerve locations. ( A ) Immunohistochemical (IHC) imaging of VEGFA and ( B ) quantification of VEGFA mean integrated density (n = 6). ( C ) IHC staining for NGF and ( D ) quantification of NGF mean integrated density (n = 6). ( E ) IF staining for macrophages (F4/80) and ( F ) quantification of macrophage number per 10 4 μm 2 (n = 6). ( G ) IF staining for scar tissue (α-SMA) and ( H ) quantification of α-SMA -positive area percentage (n = 6). ( I ) IF staining for myelin sheath (MBP) and axon (NF200) and ( J ) quantification of myelin sheath to axon area ratio (n = 6). ( K ) IF staining for pain-related mediators CGRP and TRPA1 and ( L ) quantification of CGRP (n = 6), and ( M ) TRPA1 (n = 6). Mean values are shown and error bars represent ± s.d., as analyzed by one-way ANOVA followed by the Tukey-Kramer test in ( B , D , F , H , J , L and M ). Biological replicates were used for all experiments. ns, p > 0.05, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
Figure Legend Snippet: Expression of pain signal proteins in peripheral nerve locations. ( A ) Immunohistochemical (IHC) imaging of VEGFA and ( B ) quantification of VEGFA mean integrated density (n = 6). ( C ) IHC staining for NGF and ( D ) quantification of NGF mean integrated density (n = 6). ( E ) IF staining for macrophages (F4/80) and ( F ) quantification of macrophage number per 10 4 μm 2 (n = 6). ( G ) IF staining for scar tissue (α-SMA) and ( H ) quantification of α-SMA -positive area percentage (n = 6). ( I ) IF staining for myelin sheath (MBP) and axon (NF200) and ( J ) quantification of myelin sheath to axon area ratio (n = 6). ( K ) IF staining for pain-related mediators CGRP and TRPA1 and ( L ) quantification of CGRP (n = 6), and ( M ) TRPA1 (n = 6). Mean values are shown and error bars represent ± s.d., as analyzed by one-way ANOVA followed by the Tukey-Kramer test in ( B , D , F , H , J , L and M ). Biological replicates were used for all experiments. ns, p > 0.05, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

Techniques Used: Expressing, Immunohistochemical staining, Imaging, Immunohistochemistry, Staining

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Western Blot:

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REAGENT or RESOURCE SOURCE IDENTIFIER Anti-phospho-NF-κB p65 Cell Signaling Technology Cat#3033; clone 93H1; RRID: AB_331284 Anti-IκBα antibody Cell Signaling Technology Cat#4814; clone L35A5; RRID: AB_390781 Anti-Tubulin β antibody Bioworld Cat#AP0064; RRID: AB_2797447 Anti-GAPDH antibody Servicebio Cat#GB15004-100; clone: 6C4F6; RRID: AB_2943040 HRP-conjugated goat anti-rabbit IgG secondary antibody Bioworld Cat#BS13278; RRID: AB_2773728 HRP-conjugated goat anti-mouse IgG secondary antibody for western blot Bioworld Cat#BS12478; RRID: AB_2773727 Anti-α-SMA antibody Proteintech Cat14395-1-AP; RRID: AB_2223009 Anti-mouse CD45-FITC antibody Invitrogen Cat#11-0451-85; clone 30-F11; RRID: AB_465051 Anti-mouse CD45-Alexa Fluor 700 antibody Invitrogen Cat#56-0451-82; clone 30-F11; RRID: AB_891454 Anti-mouse CD45-Brilliant Violet 785 antibody BioLegend Cat#103149; clone 30-F11; RRID: AB_2564590 Anti-mouse CD45-Brilliant Ultra Violet 496 antibody Invitrogen Cat#364-0451-82; clone 30-F11; RRID: AB_2925333 Anti-mouse CD45-Brilliant Ultra Violet 395 antibody Invitrogen Cat#363-0451-82; clone 30-F11; RRID: AB_2925264 Anti-mouse CD3-APC/Cyanine7 antibody BioLegend Cat#100221; clone 17A2; RRID: AB_2057374 Anti-mouse CD3-Brilliant Violet 510 antibody BioLegend Cat#100233; clone 17A2; RRID: AB_2561387 Anti-mouse CD3-FITC antibody Invitrogen Cat#11-0031-82; clone 145-2C11; RRID: AB_464882 Anti-mouse CD3-PerCP-Cy5.5 antibody BioLegend Cat#100328; clone 145-2C11; RRID: AB_893320 Anti-mouse CD8a-APC antibody Invitrogen Cat#17-0081-82; clone 53-6.7; RRID: AB_469335 Anti-mouse Granzyme B-PE-Cyanine7 antibody Invitrogen Cat#25-8898-82; clone NGZB; RRID: AB_10853339 Anti-mouse IFN-γ-PE antibody Invitrogen Cat#12-7311-82; clone XMG1.2; RRID: AB_466193 Anti-mouse T-bet-PE-Cyanine7 antibody Invitrogen Cat#25-5825-80; clone e 4B10; RRID: AB_11042699 Anti-mouse TIGIT-Super Bright 702 antibody Invitrogen Cat#67-9501-82; clone GIGD7; RRID: AB_2723713 Anti-mouse PD-1-PerCP-eFluor 710 antibody Invitrogen Cat#46-9985-82; clone J43; RRID: AB_11150055 Anti-mouse CD4-Brilliant Ultra Violet 737 antibody Invitrogen Cat#367-0041-82; clone GK1.5; RRID: AB_2895921 Anti-mouse CD4-FITC antibody BioLegend Cat#100406; clone GK1.5; RRID: AB_312691 Anti-mouse FOXP3-FITC antibody Invitrogen Cat#11-5773-82; clone FJK-16s; RRID: AB_465243 Anti-mouse CD25-Super Bright 436 antibody Invitrogen Cat#62-0251-82; clone PC61.5; RRID: AB_2734937 Anti-mouse CD49b-PE antibody BioLegend Cat#108908; clone DX5; RRID: AB_313415 (Continued on next page) ll OPEN ACCESS Article e2 Cell Host & Microbe 34, 1–18.e1–e18, November 11, 2026 .. REAGENT or RESOURCE SOURCE IDENTIFIER Anti-mouse Ki-67-FITC antibody Invitrogen Cat#11-5698-82; clone SolA15; RRID: AB_11151330 Anti-mouse CD11b-Brilliant Violet 605 antibody Invitrogen Cat#406-0112-82; clone M1/70; RRID: AB_2937154 Anti-mouse CD11b-Brilliant Violet 650 antibody Invitrogen Cat#416-0112-82; clone M1/70; RRID: AB_2925670 Anti-mouse F4/80-APC antibody BioLegend Cat#123116; clone BM8; RRID: AB_893481 Anti-mouse C1q-PE antibody CEDARLANE Cat#CL7501PE; clone RmC7H8; RRID: AB_10557399 Anti-mouse CD11c-eFluor 450 antibody Invitrogen Cat#48-0114-82; clone N418; RRID: AB_1548654 Anti-mouse MHC Class II-Brilliant Ultra Violet 737 antibody Invitrogen Cat#367-5321-82; clone M5/114.15.2; RRID: AB_2896014 Anti-mouse MHC Class II-PerCP-Cy5.5 antibody BD Biosciences Cat#562363; clone M5/114.15.2; RRID: AB_11153297 Anti-mouse CD86-PE-Cyanine7 antibody Invitrogen Cat#25-0862-80; clone GL1; RRID: AB_2573372 Anti-mouse Ly-6C-PerCP-Cyanine5.5 antibody Invitrogen Cat#45-5932-82; clone HK1.4; RRID: AB_2723343 Anti-mouse Ly-6C-PE/Cyanine7 antibody BioLegend Cat#128017; clone HK1.4; RRID: AB_1732093 Anti-mouse Ly-6G-Brilliant Violet 421 antibody Invitrogen Cat#404-9668-80; clone 1A8-Ly6g; RRID: AB_2925554 Anti-mouse Ly-6G-APC antibody BioLegend Cat#127613; clone 1A8; RRID: AB_1877163 Anti-human CD45-eFluor 506 antibody Invitrogen Cat#69-0459-42; clone HI30; RRID: AB_2637382 Anti-human CD3-Brilliant Ultra Violet 496 antibody Invitrogen Cat#364-0036-42; clone SK7; RRID: AB_2925315 Anti-human CD8a-FITC antibody Invitrogen Cat#11-0088-42; clone RPA-T8; RRID: AB_10669559 Anti-human Granzyme B-PE antibody Invitrogen Cat#12-8896-42; clone N4TL33; RRID: AB_2724394 Anti-human Perforin-APC antibody Invitrogen Cat#17-9994-42; clone dG9 (delta G9); RRID: AB_10853967 Anti-human PD-1-PE-Cyanine7 antibody Invitrogen Cat#25-2799-42; clone eBioJ105 (J105); RRID: AB_10853804 Anti-human TIGIT-APC antibody Invitrogen Cat#17-9500-42; clone MBSA43; RRID: AB_2573305 Anti-human Ki-67-Brilliant Violet 421 antibody Invitrogen Cat#404-5698-82; clone SolA15; RRID: AB_2925532 Bacterial and virus strains Akkermansia muciniphila ATCC BAA-835 Guangdong Microbial Culture Collection Center (GDMCC) Cat#1.1346 Bacteroides thetaiotaomicron ATCC 29148 Huizao Biotechnology Cat#HZB725168 Ruminococcus torques ATCC 27756 Huizao Biotechnology Cat#HZB358784 Escherichia coli BL21(DE3) competent cells Sangon Biotech Cat#B528414 Biological samples Human fecal samples from patients with CRC and healthy individuals This paper; West China Hospital of Sichuan University N/A Human CRC tumor tissues and matched adjacent normal tissues This paper; West China Hospital of Sichuan University N/A (Continued on next page) ll OPEN ACCESSArticle Cell Host & Microbe 34, 1–18.e1–e18, November 11, 2026 e3

Incubation:

Article Title: Myf5 Progenitors Define the Lineage Identity of Somitic Vascular Smooth Muscle Cells.
Article Snippet: .. Sections were blocked with 5% bovine serum albumin (BSA) or normal goat serum for 1 h at room temperature, followed by overnight incubation at 4 ◦C with primary antibodies: anti-α-SMA (Proteintech, 14395-1-AP), anti-Ki67 (Abcam, ab15580), and anti-CD31 (R&D, AF3628), anti-PDGFRα (R&D, MAB3221), anti-OPN (R&D, AF808). ..

Article Title: FGF21-NR1D1 Signaling Restrains the CYP4A/20-HETE/GPR75 Axis to Counteract Integrated Renal-Vascular Injury in Hypertension.
Article Snippet: Samples were separated by SDS-PAGE and transferred to PVDF membranes (Millipore, ISEQ00010). .. Membranes were blocked with 5% non-fat dry milk (BD, 232100) in TBST for 1.5 h at room temperature, followed by overnight incubation with primary antibodies: FGF21 (Abcam, ab171941), CYP4A/CYP4A11 (Abcam, ab3573), Collagen I (Abcam, ab184996), J ur na l P -p ro of IL-6 (Abclonal, A0286), GPR75 (Abmart, PA2521), NR1D1 (Santa Cruz, sc-100910), ERK1/2 (Cell Signaling Technology, 9102S), p-ERK1/2 (Cell Signaling Technology, 4370S), fibronectin (Proteintech, 15613-1-AP), α-SMA (Proteintech, 14395-1-AP), GAPDH (Proteintech, 10494-1-AP), and β-actin (Bioworld, AP0060). ..

Article Title: Repetitive pulsed magnetic stimulation attenuates neurogenic erectile dysfunction associated with the upregulation of the BDNF/NGF axis in a rat model of cavernous nerve injury.
Article Snippet: .. The following primary antibodies were incubated overnight at 4°C: anti-α-SMA (1:5000; 14395-1-AP; Proteintech, Wuhan, China), anti-B-cell lymphoma 2 (Bcl-2; 1:3000; A27315PM; ABclonal), anti-Caspase-3 (1:5000; A19664; ABclonal), anti-Bcl-2 associated X protein (Bax; 1:1000; A0207; ABclonal), and anti-glyceraldehyde-3-phosphate dehydrogenase (GAPDH; 1:50 000; ET1601-4; HUABIO, Hangzhou, China). ..

Article Title: Tirzepatide Attenuates Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension: Association with the SIRT1/H4K12la/c-Jun Axis.
Article Snippet: The sections were blocked with normal goat serum (31872, ThermoFisher, Waltham, MA, USA) for 1 h at room temperature. .. Slides were then incubated overnight at 4 ◦C with a primary antibody against α-SMA (14395-1-AP, Proteintech, Wuhan, China). .. After rigorous washing with PBS, sections were incubated with the corresponding secondary antibody and visualized using a DAB substrate kit (ab64238, Abcam, Cambridge, UK).

other:

Article Title: NAT10 exacerbates aortic valve calcification via PCSK9 mRNA ac4C acetylation
Article Snippet: anti-α-SMA , Proteintech , Cat#14395-1-AP; RRID: AB_2223009.



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