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Sangon Biotech ascorbic acid
Ascorbic Acid, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ascorbate+acid/acid+ascorbic+l/pm42301525-41-0-20
Average 86 stars, based on 1 article reviews
ascorbic acid - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Indirect Immunoperoxidase Assay:

Article Title: Fluorescent and colorimetric detection of Vibrio anguillarum based on loop-mediated isothermal amplification coupled with copper nanoclusters sensing system.
Article Snippet: 1 State Key Laboratory of Marine Food Processing and Safety Control, College of Food Science and Engineering, Ocean University of China, Qingdao 266404, China 2 Laboratory for Marine Drugs and Bioproducts, Qingdao Marine Science and Technology Center, Qingdao 266237, China 3 School of Materials Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China Abstract Vibrio anguillarum poses a serious threat to food safety, human health and aquaculture.. At present, sensitive visual detection methods for V. anguillarum remain scarce.. In this study, a novel dual-signal sensing system was constructed for the highly specific and visual detection of V. anguillarum.

other:

Article Title: Sequential Extraction of Naringin and Low-Ester Pectin from Naturally Dropped Fruit of Pomelo
Article Snippet: Citric acid, lactic acid, potassium persulfate, ferrous sulfate heptahydrate, salicylic acid, ascorbic acid (V C ), and naringin were bought from Sangon Biotech (Shanghai) Co., Ltd., Shanghai, China.

Article Title: Rapid and ultrasensitive detection of quinolone antibiotics by ratiometric fluorescence sensing integrated with redox cycling signal amplification.
Article Snippet: • A ratiometric fluorescence probe was developed based on GSH-CuNCs/DAP.. • The redox cycling signal amplification delivers high sensitivity.. • The internal filtration effect (IFE) delivers high specificity.

Control:

Article Title: A spatiotemporal hypergraph self-attention neural networks framework for the identification and pharmacological efficacy assessment of Parkinson’s disease motor symptoms
Article Snippet: To establish a unilateral dopamine depletion model, mice were administered bilateral injections of 6-hydroxydopamine hydrochloride (6-OHDA-HCl, Sigma-Aldrich) into the left striatum. .. The control group received an equivalent volume of saline containing 0.02% ascorbic acid (Sangon Biotech) at the same injection sites. .. Mice were anesthetized with 3–4% isoflurane (RWD Life Science) during induction and maintained under 1–1.5% isoflurane for the duration of the surgery.

Saline:

Article Title: A spatiotemporal hypergraph self-attention neural networks framework for the identification and pharmacological efficacy assessment of Parkinson’s disease motor symptoms
Article Snippet: To establish a unilateral dopamine depletion model, mice were administered bilateral injections of 6-hydroxydopamine hydrochloride (6-OHDA-HCl, Sigma-Aldrich) into the left striatum. .. The control group received an equivalent volume of saline containing 0.02% ascorbic acid (Sangon Biotech) at the same injection sites. .. Mice were anesthetized with 3–4% isoflurane (RWD Life Science) during induction and maintained under 1–1.5% isoflurane for the duration of the surgery.

Injection:

Article Title: A spatiotemporal hypergraph self-attention neural networks framework for the identification and pharmacological efficacy assessment of Parkinson’s disease motor symptoms
Article Snippet: To establish a unilateral dopamine depletion model, mice were administered bilateral injections of 6-hydroxydopamine hydrochloride (6-OHDA-HCl, Sigma-Aldrich) into the left striatum. .. The control group received an equivalent volume of saline containing 0.02% ascorbic acid (Sangon Biotech) at the same injection sites. .. Mice were anesthetized with 3–4% isoflurane (RWD Life Science) during induction and maintained under 1–1.5% isoflurane for the duration of the surgery.

MTT Assay:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Multiple Displacement Amplification:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Cell Culture:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Activity Assay:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Staining:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

TUNEL Assay:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

ATP Assay:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Western Blot:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Bioprocessing:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.

Synthesized:

Article Title: Multi-Targeting Effects and Orchestrated Induction of Multiple Cell Death Modalities by Silver-Copper Alloy Nanoparticles Functionalized Drug Nanocrystals in Cancer Cells.
Article Snippet: To combat multidrug resistance and cancer stem cell (CSC) persistence, we constructed a tumor-targeted nanoplatform integrating silver/copper alloy nanoparticles (Cu−Ag NPs) and camptothecin (CPT) nanocrystals for synergistic multimodal therapy.. The nanocomposite was fabricated by stepwise assembly of CPT nanocrystals, a polydopamine coating, and functionalization with Cu−Ag NPs plus a tumor-mitochondria dual-targeting peptide.. It exhibited a hydrodynamic diameter of ∼152.67 nm, high colloidal stability, favorable photothermal performance, and pH/NIRresponsive drug release.



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