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pdgf rabbit pab  (Proteintech)


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    Structured Review

    Proteintech pdgf rabbit pab
    Pdgf Rabbit Pab, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pdgf rabbit pab/product/Proteintech
    Average 94 stars, based on 13 article reviews
    pdgf rabbit pab - by Bioz Stars, 2026-03
    94/100 stars

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    Fig. 3. MiR-146b-5p up-regulation inhibited proliferation of pericytes in mice with lung fibrosis. (A) Pericytes were identified by CD13 and <t>PDGFRβ</t> staining. (B) Pericytes were transfected with NC mimics or miR-146b-5p mimics. The level of miR-146b-5p in the pericytes was assessed by RT-qPCR. (C) The viability of pericytes was assessed by CCK8 assay. (D) The cell cycle distribution was assessed by flow cytometry. (E) The expression of α-SMA and NG2 in the pericytes was evaluated by immunofluorescence staining. *P < 0.05.
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    The proteins from tail-amputated E. foetida affect secretion of factors about wound healing. (A, B) Representative immunoblot images depict <t>PDGF</t> or TGF-β ( n = 5). (C, D) Immunohistochemical results of rat wound. The IOD of PDGF or TGF-β on skin wounds. (E) The HYP expression of rats’ skin wounds ( n = 5). The results are presented as mean ± S.E.M. Compared with the blank control group, * P < 0.05, ** P < 0.01; compared with the un-amputated group, # P < 0.05.
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    Image Search Results


    Fig. 3. MiR-146b-5p up-regulation inhibited proliferation of pericytes in mice with lung fibrosis. (A) Pericytes were identified by CD13 and PDGFRβ staining. (B) Pericytes were transfected with NC mimics or miR-146b-5p mimics. The level of miR-146b-5p in the pericytes was assessed by RT-qPCR. (C) The viability of pericytes was assessed by CCK8 assay. (D) The cell cycle distribution was assessed by flow cytometry. (E) The expression of α-SMA and NG2 in the pericytes was evaluated by immunofluorescence staining. *P < 0.05.

    Journal: Folia biologica

    Article Title: Up-regulation of MiR-146b-5p Inhibits Fibrotic Lung Pericytes via Inactivation of the Notch1/PDGFRβ/ROCK1 Pathway.

    doi: 10.14712/fb2022068050180

    Figure Lengend Snippet: Fig. 3. MiR-146b-5p up-regulation inhibited proliferation of pericytes in mice with lung fibrosis. (A) Pericytes were identified by CD13 and PDGFRβ staining. (B) Pericytes were transfected with NC mimics or miR-146b-5p mimics. The level of miR-146b-5p in the pericytes was assessed by RT-qPCR. (C) The viability of pericytes was assessed by CCK8 assay. (D) The cell cycle distribution was assessed by flow cytometry. (E) The expression of α-SMA and NG2 in the pericytes was evaluated by immunofluorescence staining. *P < 0.05.

    Article Snippet: To isolate pericytes, cells were incubated with anti-PDGFRβ polyclonal antibody (#3169, Cell Signaling Technology, Danvers, MA).

    Techniques: Staining, Transfection, Quantitative RT-PCR, CCK-8 Assay, Flow Cytometry, Expressing, Immunofluorescence

    Fig. 4. Up-regulation of miR-146b-5p inhibited the fibrosis in pericytes through inactivation of the Notch1/PDGFRβ/ ROCK1 pathway. (A) The mRNA levels of Notch1, PDGFRβ and ROCK1 in the pericytes of mice with lung fibrosis were investigated by RT-qPCR. (B) The protein levels of Notch1, PDGFRβ and ROCK1 in the pericytes of mice with lung fi- brosis were assessed by Western blot. *P < 0.05.

    Journal: Folia biologica

    Article Title: Up-regulation of MiR-146b-5p Inhibits Fibrotic Lung Pericytes via Inactivation of the Notch1/PDGFRβ/ROCK1 Pathway.

    doi: 10.14712/fb2022068050180

    Figure Lengend Snippet: Fig. 4. Up-regulation of miR-146b-5p inhibited the fibrosis in pericytes through inactivation of the Notch1/PDGFRβ/ ROCK1 pathway. (A) The mRNA levels of Notch1, PDGFRβ and ROCK1 in the pericytes of mice with lung fibrosis were investigated by RT-qPCR. (B) The protein levels of Notch1, PDGFRβ and ROCK1 in the pericytes of mice with lung fi- brosis were assessed by Western blot. *P < 0.05.

    Article Snippet: To isolate pericytes, cells were incubated with anti-PDGFRβ polyclonal antibody (#3169, Cell Signaling Technology, Danvers, MA).

    Techniques: Quantitative RT-PCR, Western Blot

    The proteins from tail-amputated E. foetida affect secretion of factors about wound healing. (A, B) Representative immunoblot images depict PDGF or TGF-β ( n = 5). (C, D) Immunohistochemical results of rat wound. The IOD of PDGF or TGF-β on skin wounds. (E) The HYP expression of rats’ skin wounds ( n = 5). The results are presented as mean ± S.E.M. Compared with the blank control group, * P < 0.05, ** P < 0.01; compared with the un-amputated group, # P < 0.05.

    Journal: ACS Omega

    Article Title: Promoted Skin Wound Healing by Tail-Amputated Eisenia foetida Proteins via the Ras/Raf/MEK/ERK Signaling Pathway

    doi: 10.1021/acsomega.3c00317

    Figure Lengend Snippet: The proteins from tail-amputated E. foetida affect secretion of factors about wound healing. (A, B) Representative immunoblot images depict PDGF or TGF-β ( n = 5). (C, D) Immunohistochemical results of rat wound. The IOD of PDGF or TGF-β on skin wounds. (E) The HYP expression of rats’ skin wounds ( n = 5). The results are presented as mean ± S.E.M. Compared with the blank control group, * P < 0.05, ** P < 0.01; compared with the un-amputated group, # P < 0.05.

    Article Snippet: Sections were blocked with normal goat serum for 30 min. Tissues were reacted with TGF-β1 Rabbit Polyclonal antibody (1: 6000, Proteintech, China) or PDGF Rabbit Polyclonal antibody (1: 5000, Proteintech, China) at 4 °C overnight.

    Techniques: Western Blot, Immunohistochemical staining, Expressing, Control