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pperk  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc pperk
    Pperk, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1352 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pperk/product/Cell Signaling Technology Inc
    Average 97 stars, based on 1352 article reviews
    pperk - by Bioz Stars, 2026-03
    97/100 stars

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    Cell Signaling Technology Inc antibodies against pperk
    Fig. 4. SB supplement ameliorated TMAO-mediated activation of ER stress signaling and dysregulation of ionic signaling. (A) and (B) Representative images and statistical data show the expression of <t>pPERK,</t> <t>PERK,</t> <t>pIRE1a,</t> IRE1a, pNF-jB, NF-jB, pIP3R, IP3R, NCX, Kv1.5, and b-actin in HL-1 cells from control group (n = 3), TMAO treated (n = 3), SB treated (n = 3), and TMAO combined with SB treated group (n = 3) in three independent experiments. b-Actin was used as a loading control. *P < 0.05. **P < 0.01. TMAO versus control or SB or TMAO combined with SB treatment.
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    Image Search Results


    Fig. 4. SB supplement ameliorated TMAO-mediated activation of ER stress signaling and dysregulation of ionic signaling. (A) and (B) Representative images and statistical data show the expression of pPERK, PERK, pIRE1a, IRE1a, pNF-jB, NF-jB, pIP3R, IP3R, NCX, Kv1.5, and b-actin in HL-1 cells from control group (n = 3), TMAO treated (n = 3), SB treated (n = 3), and TMAO combined with SB treated group (n = 3) in three independent experiments. b-Actin was used as a loading control. *P < 0.05. **P < 0.01. TMAO versus control or SB or TMAO combined with SB treatment.

    Journal: Journal of advanced research

    Article Title: Short-chain fatty acid butyrate against TMAO activating endoplasmic-reticulum stress and PERK/IRE1-axis with reducing atrial arrhythmia.

    doi: 10.1016/j.jare.2024.08.009

    Figure Lengend Snippet: Fig. 4. SB supplement ameliorated TMAO-mediated activation of ER stress signaling and dysregulation of ionic signaling. (A) and (B) Representative images and statistical data show the expression of pPERK, PERK, pIRE1a, IRE1a, pNF-jB, NF-jB, pIP3R, IP3R, NCX, Kv1.5, and b-actin in HL-1 cells from control group (n = 3), TMAO treated (n = 3), SB treated (n = 3), and TMAO combined with SB treated group (n = 3) in three independent experiments. b-Actin was used as a loading control. *P < 0.05. **P < 0.01. TMAO versus control or SB or TMAO combined with SB treatment.

    Article Snippet: The cells were fixed with 100 % methanol, the slides were blocked with 5 % bovine serum albumin, and the cells were incubated with primary antibodies against pPERK (#3179, Cell Signaling), pIRE1a (NB100-2323, Novus), pNF-jB (ab86299, Abcam), and calnexin (ab22595, Abcam) and secondary antibodies (Alexa Fluor488 and Alexa Fluor 647 Jackson) in blocking buffer.

    Techniques: Activation Assay, Expressing, Control

    Fig. 5. SB supplement ameliorated TMAO-mediated overexpression of ER stress signaling and pNF-jB in HL-1 cells. (A) and (B) show the representative images and statistical data of pPERK, pIRE1a, pNF-jB, and ER marker-Calnexin expression in HL-1 cells through cellular immunostaing assay in control group (n = 3), TMAO treated (n = 3), SB treated (n = 3), and TMAO combined with SB treated group (n = 3) in three independent experiments. (bar, 25 lm). **P < 0.01. TMAO versus control or SB or TMAO combined with SB treatment.

    Journal: Journal of advanced research

    Article Title: Short-chain fatty acid butyrate against TMAO activating endoplasmic-reticulum stress and PERK/IRE1-axis with reducing atrial arrhythmia.

    doi: 10.1016/j.jare.2024.08.009

    Figure Lengend Snippet: Fig. 5. SB supplement ameliorated TMAO-mediated overexpression of ER stress signaling and pNF-jB in HL-1 cells. (A) and (B) show the representative images and statistical data of pPERK, pIRE1a, pNF-jB, and ER marker-Calnexin expression in HL-1 cells through cellular immunostaing assay in control group (n = 3), TMAO treated (n = 3), SB treated (n = 3), and TMAO combined with SB treated group (n = 3) in three independent experiments. (bar, 25 lm). **P < 0.01. TMAO versus control or SB or TMAO combined with SB treatment.

    Article Snippet: The cells were fixed with 100 % methanol, the slides were blocked with 5 % bovine serum albumin, and the cells were incubated with primary antibodies against pPERK (#3179, Cell Signaling), pIRE1a (NB100-2323, Novus), pNF-jB (ab86299, Abcam), and calnexin (ab22595, Abcam) and secondary antibodies (Alexa Fluor488 and Alexa Fluor 647 Jackson) in blocking buffer.

    Techniques: Over Expression, Marker, Expressing, Control

    Fig. 8. SB supplement ameliorated atrial fibrosis and PERK/IRE1a/NF-jB axis of TMAO-treated mice. The expression of atrial fibrosis (blue area) was detected by Masson’s staining and immunostaining of pPERK, pIRE1a, and pNF-jB in the atrium tissues derived from mice gavage with control (n = 5), TMAO (n = 5), and TMAO combined with SB (n = 5). The expressions of pPERK are indicated by hollow arrowheads. (bar, 25 lm). ** p < 0.01. TMAO treatment versus control group or TMAO combined with SB treated group. (For interpretation of the references to colour in this Fig. legend, the reader is referred to the web version of this article.)

    Journal: Journal of advanced research

    Article Title: Short-chain fatty acid butyrate against TMAO activating endoplasmic-reticulum stress and PERK/IRE1-axis with reducing atrial arrhythmia.

    doi: 10.1016/j.jare.2024.08.009

    Figure Lengend Snippet: Fig. 8. SB supplement ameliorated atrial fibrosis and PERK/IRE1a/NF-jB axis of TMAO-treated mice. The expression of atrial fibrosis (blue area) was detected by Masson’s staining and immunostaining of pPERK, pIRE1a, and pNF-jB in the atrium tissues derived from mice gavage with control (n = 5), TMAO (n = 5), and TMAO combined with SB (n = 5). The expressions of pPERK are indicated by hollow arrowheads. (bar, 25 lm). ** p < 0.01. TMAO treatment versus control group or TMAO combined with SB treated group. (For interpretation of the references to colour in this Fig. legend, the reader is referred to the web version of this article.)

    Article Snippet: The cells were fixed with 100 % methanol, the slides were blocked with 5 % bovine serum albumin, and the cells were incubated with primary antibodies against pPERK (#3179, Cell Signaling), pIRE1a (NB100-2323, Novus), pNF-jB (ab86299, Abcam), and calnexin (ab22595, Abcam) and secondary antibodies (Alexa Fluor488 and Alexa Fluor 647 Jackson) in blocking buffer.

    Techniques: Expressing, Staining, Immunostaining, Derivative Assay, Control