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immpress ap horse anti goat igg polymer detection kit  (Vector Laboratories)


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    Vector Laboratories immpress ap horse anti goat igg polymer detection kit
    Immpress Ap Horse Anti Goat Igg Polymer Detection Kit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immpress ap horse anti goat igg polymer detection kit/product/Vector Laboratories
    Average 93 stars, based on 19 article reviews
    immpress ap horse anti goat igg polymer detection kit - by Bioz Stars, 2026-05
    93/100 stars

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    Xing-Pi-Qing-Gan decoction attenuates ethanol-induced dysfunction in HepG2. A and B: Quantitation of cell viability of HepG2 cells treated with ethanol (A) and with Xing-Pi-Qing-Gan decoction (B) was determined by CCK-8 assay; C: HepG2 alanine aminotransferase, aspartate aminotransferase, triglyceride and alkaline phosphatase levels; D: Oil Red O staining, images were taken (40 ×); E: Relative mRNA levels of lipogenesis; F-H: Relative mRNA levels and relative protein expression of inflammation; I: Relative mRNA levels of Apoptosis; J and K: Relative protein expression of Bcl-2 , Caspase-3 in HepG2 ( n = 3-5). a P < 0.05 vs the control group; b P < 0.01 vs the control group; c P < 0.05 vs the ethanol-fed group; d P < 0.01 vs the ethanol-fed group. Ctr: Control; EtOH: Ethanol-fed; XPQG: Xing-Pi-Qing-Gan decoction; AST: Aspartate aminotransferase; ALT: Alanine aminotransferase; TG: Triglyceride; TC: Total cholesterol; AKP: Alkaline phosphatase; XPQG-L: Xing-Pi-Qing-Gan decoction-low; XPQG-M: Xing-Pi-Qing-Gan decoction-medium; XPQG-H: Xing-Pi-Qing-Gan decoction-high; IL-6: Interleukin-6; IL-1β: Interleukin-1β; TNF-α : Tumor necrosis factor-α.

    Journal: World Journal of Gastroenterology

    Article Title: Xing-Pi-Qing-Gan decoction alleviates alcoholic liver disease by down-regulating DDIT3 and restoring Nrf2 / HO-1 antioxidant signaling: Multi-omics and experimental evidence

    doi: 10.3748/wjg.v32.i8.115077

    Figure Lengend Snippet: Xing-Pi-Qing-Gan decoction attenuates ethanol-induced dysfunction in HepG2. A and B: Quantitation of cell viability of HepG2 cells treated with ethanol (A) and with Xing-Pi-Qing-Gan decoction (B) was determined by CCK-8 assay; C: HepG2 alanine aminotransferase, aspartate aminotransferase, triglyceride and alkaline phosphatase levels; D: Oil Red O staining, images were taken (40 ×); E: Relative mRNA levels of lipogenesis; F-H: Relative mRNA levels and relative protein expression of inflammation; I: Relative mRNA levels of Apoptosis; J and K: Relative protein expression of Bcl-2 , Caspase-3 in HepG2 ( n = 3-5). a P < 0.05 vs the control group; b P < 0.01 vs the control group; c P < 0.05 vs the ethanol-fed group; d P < 0.01 vs the ethanol-fed group. Ctr: Control; EtOH: Ethanol-fed; XPQG: Xing-Pi-Qing-Gan decoction; AST: Aspartate aminotransferase; ALT: Alanine aminotransferase; TG: Triglyceride; TC: Total cholesterol; AKP: Alkaline phosphatase; XPQG-L: Xing-Pi-Qing-Gan decoction-low; XPQG-M: Xing-Pi-Qing-Gan decoction-medium; XPQG-H: Xing-Pi-Qing-Gan decoction-high; IL-6: Interleukin-6; IL-1β: Interleukin-1β; TNF-α : Tumor necrosis factor-α.

    Article Snippet: Aspartate aminotransferase (AST) detection kit, alanine aminotransferase (ALT) detection kit, triglyceride (TG) detection kit, malondialdehyde (MDA) detection kit, alkaline phosphatase (AKP) detection kit, superoxide dismutase (SOD) detection kit, and γ-glutamyl transferase (GGT) detection kit were obtained from Nanjing Jiancheng Bioengineering Research Institute (Nanjing, China).

    Techniques: Quantitation Assay, CCK-8 Assay, Staining, Expressing, Control

    DDIT3 knocked-down confirms its role in Xing-Pi-Qing-Gan decoction -mediated protection. A: The effects of Xing-Pi-Qing-Gan decoction (XPQG) on alanine aminotransferase, aspartate aminotransferase, triglyceride, total cholesterol, and alkaline phosphatase expression in HepG2 cells as transfected with DDIT3 siRNA; B: After transfected with DDIT3 siRNA, XPQG had no obvious effect on the expression of superoxide dismutase and glutathione; C: Transcript levels of DDIT3 were measured by quantitative RT-PCR in HepG2 cells as transfected with DDIT3 siRNA; D: Relative mRNA levels of p38 , Nrf2 and HO-1 in HepG2 cells as transfected with DDIT3 siRNA; E and F: Relative protein expression of DDIT3, p38, Nrf2 and HO-1 in HepG2 cells as transfected with DDIT3 siRNA; G: Effects of XPQG on the expression of inflammatory factors in HepG2 in HepG2 cells as transfected with DDIT3 siRNA; H: Relative mRNA levels of SREBP1-c and ACC in HepG2 cells as transfected with DDIT3 siRNA; I: Effects of XPQG on the expression of Apoptosis in HepG2 cells as transfected with DDIT3 siRNA ( n = 3-5). a P < 0.01 vs si-DDIT3 group; b P < 0.01 vs negative control group; c P < 0.05 vs the si-DDIT3 group. ALT: Alanine aminotransferase; TG: Triglyceride; TC: Total cholesterol; AKP: Alkaline phosphatase; SOD: Superoxide dismutase; GSH: Glutathione; NC: Negative control; IL-6: Interleukin-6; EtOH: Ethanol-fed; XPQG: Xing-Pi-Qing-Gan decoction.

    Journal: World Journal of Gastroenterology

    Article Title: Xing-Pi-Qing-Gan decoction alleviates alcoholic liver disease by down-regulating DDIT3 and restoring Nrf2 / HO-1 antioxidant signaling: Multi-omics and experimental evidence

    doi: 10.3748/wjg.v32.i8.115077

    Figure Lengend Snippet: DDIT3 knocked-down confirms its role in Xing-Pi-Qing-Gan decoction -mediated protection. A: The effects of Xing-Pi-Qing-Gan decoction (XPQG) on alanine aminotransferase, aspartate aminotransferase, triglyceride, total cholesterol, and alkaline phosphatase expression in HepG2 cells as transfected with DDIT3 siRNA; B: After transfected with DDIT3 siRNA, XPQG had no obvious effect on the expression of superoxide dismutase and glutathione; C: Transcript levels of DDIT3 were measured by quantitative RT-PCR in HepG2 cells as transfected with DDIT3 siRNA; D: Relative mRNA levels of p38 , Nrf2 and HO-1 in HepG2 cells as transfected with DDIT3 siRNA; E and F: Relative protein expression of DDIT3, p38, Nrf2 and HO-1 in HepG2 cells as transfected with DDIT3 siRNA; G: Effects of XPQG on the expression of inflammatory factors in HepG2 in HepG2 cells as transfected with DDIT3 siRNA; H: Relative mRNA levels of SREBP1-c and ACC in HepG2 cells as transfected with DDIT3 siRNA; I: Effects of XPQG on the expression of Apoptosis in HepG2 cells as transfected with DDIT3 siRNA ( n = 3-5). a P < 0.01 vs si-DDIT3 group; b P < 0.01 vs negative control group; c P < 0.05 vs the si-DDIT3 group. ALT: Alanine aminotransferase; TG: Triglyceride; TC: Total cholesterol; AKP: Alkaline phosphatase; SOD: Superoxide dismutase; GSH: Glutathione; NC: Negative control; IL-6: Interleukin-6; EtOH: Ethanol-fed; XPQG: Xing-Pi-Qing-Gan decoction.

    Article Snippet: Aspartate aminotransferase (AST) detection kit, alanine aminotransferase (ALT) detection kit, triglyceride (TG) detection kit, malondialdehyde (MDA) detection kit, alkaline phosphatase (AKP) detection kit, superoxide dismutase (SOD) detection kit, and γ-glutamyl transferase (GGT) detection kit were obtained from Nanjing Jiancheng Bioengineering Research Institute (Nanjing, China).

    Techniques: Expressing, Transfection, Quantitative RT-PCR, Negative Control