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polyclonal rabbit anti-rat α-sma  (Boster Bio)


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    Boster Bio polyclonal rabbit anti-rat α-sma
    Polyclonal Rabbit Anti Rat α Sma, supplied by Boster Bio, 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/result/polyclonal rabbit anti-rat α-sma/product/Boster Bio
    Average 90 stars, based on 1 article reviews
    polyclonal rabbit anti-rat α-sma - by Bioz Stars, 2026-03
    90/100 stars

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    Pathological and immunohistochemical results between the control and the experimental groups. (A) . The HE staining (400ⅹ). (B) . The Masson staining (400ⅹ), the fibrosis area was calculated by ImageJ software, and there was significant statistical difference between the two groups (** p < .01). (C) . Immunohistochemical staining of smooth muscle specific marker <t>α</t> <t>-SMA</t> was compared between the two groups.
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    Pathological and immunohistochemical results between the control and the experimental groups. (A) . The HE staining (400ⅹ). (B) . The Masson staining (400ⅹ), the fibrosis area was calculated by ImageJ software, and there was significant statistical difference between the two groups (** p < .01). (C) . Immunohistochemical staining of smooth muscle specific marker α -SMA was compared between the two groups.

    Journal: Frontiers in Physiology

    Article Title: Characteristics and transcriptomic analysis of scar tissues on the inner uterine cavity wall in patients with intrauterine adhesions

    doi: 10.3389/fphys.2022.990009

    Figure Lengend Snippet: Pathological and immunohistochemical results between the control and the experimental groups. (A) . The HE staining (400ⅹ). (B) . The Masson staining (400ⅹ), the fibrosis area was calculated by ImageJ software, and there was significant statistical difference between the two groups (** p < .01). (C) . Immunohistochemical staining of smooth muscle specific marker α -SMA was compared between the two groups.

    Article Snippet: The tissue sections were deparaffinized, treated with 3% H2O2 for 25 min to inactivate endogenous peroxidases, heated in 10-mM citrate buffer at 121°C for 30 min for antigen retrieval, blocked in 5% normal serum for 20 min, and incubated with a primary polyclonal rabbit anti-rat antibody specific for α -SMA (1:200 in PBS, Servicebio; GB111364) overnight at 4°C.

    Techniques: Immunohistochemical staining, Control, Staining, Software, Marker