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dapi staining solution  (Beyotime)


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    Structured Review

    Beyotime dapi staining solution
    Dapi Staining Solution, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 2054 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dapi+stain/DAPI+Staining+Solution/pmc13097096-64-0-21
    Average 99 stars, based on 2054 article reviews
    dapi staining solution - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Incubation:

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects.
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10min, protected from light. ..

    Article Title: Efficient, High-Quality Engineering of Therapeutic Extracellular Vesicles on an Integrated Nanoplatform.
    Article Snippet: Engineered extracellular vesicles (EVs) have been recognized as important therapeutics for gene and cell therapy.. To achieve clinically desired therapy, technologies for EV engineering have high demands on the efficacy in producing EVs and their qualities, which, however, remain challenging to conventional routes due to their limited control on therapeutic payload delivery, EV secretion, and extracellular microenvironments.. Here, we report a nanoplatform (denoted as PURE) that enables efficient electro-transfection while stimulating cells to produce high-quality EVs carrying functional RNAs.

    Article Title: Trans‐Coumaryl acetate mediates GRK5/NF‐κB/Nrf2 signaling axis to ameliorate septic acute kidney injury
    Article Snippet: Cell surfaces or tissue sections were permeabilized with drops of 0.3% Tritonx‐100 (X100, Sigma‐Aldrich) for 10 min 5% bovine serum albumin (BSA, V900933, Sigma‐Aldrich) was added for closure for 30 min. NF‐κB primary antibody (14‐6731‐81, 1:100, Invitrogen) was added dropwise on the cell surface, and F4/80 primary antibody (MA5‐16363, 1:100, Invitrogen) was added dropwise on the surface of the tissue sections, and incubated overnight at 4°C. .. The next day, the tissue sections were incubated with FITC‐labeled goat anti‐rabbit IgG (F‐2765, 1:100, Invitrogen) for 1 h at 37°C away from light, and then they were exposed to DAPI stain (C1005, Beyotime) for 10 min, and observed using fluorescence microscopy. ..

    Article Title: Heterologous expression of AtLEC1 and AtLEC1-LIKE transcription factors redirects carbon flux toward lipid accumulation in diatom
    Article Snippet: .. The cell pellet was then treated with 150 μl of DAPI stain (Beyotime, C1006) and incubated for 10 min at ambient temperature. ..

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60 min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10 min, protected from light. ..

    Article Title: Heterologous expression of AtLEC1 and AtLEC1-LIKE transcription factors redirects carbon flux toward lipid accumulation in diatom.
    Article Snippet: .. The cell pellet 175 was then treated with 150 μl of DAPI stain (Beyotime, C1006) and incubated 176 for 10 minutes at ambient temperature. ..

    Saline:

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects.
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10min, protected from light. ..

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60 min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10 min, protected from light. ..

    Staining:

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects.
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10min, protected from light. ..

    Article Title: Efficient, High-Quality Engineering of Therapeutic Extracellular Vesicles on an Integrated Nanoplatform.
    Article Snippet: Engineered extracellular vesicles (EVs) have been recognized as important therapeutics for gene and cell therapy.. To achieve clinically desired therapy, technologies for EV engineering have high demands on the efficacy in producing EVs and their qualities, which, however, remain challenging to conventional routes due to their limited control on therapeutic payload delivery, EV secretion, and extracellular microenvironments.. Here, we report a nanoplatform (denoted as PURE) that enables efficient electro-transfection while stimulating cells to produce high-quality EVs carrying functional RNAs.

    Article Title: Trans‐Coumaryl acetate mediates GRK5/NF‐κB/Nrf2 signaling axis to ameliorate septic acute kidney injury
    Article Snippet: Cell surfaces or tissue sections were permeabilized with drops of 0.3% Tritonx‐100 (X100, Sigma‐Aldrich) for 10 min 5% bovine serum albumin (BSA, V900933, Sigma‐Aldrich) was added for closure for 30 min. NF‐κB primary antibody (14‐6731‐81, 1:100, Invitrogen) was added dropwise on the cell surface, and F4/80 primary antibody (MA5‐16363, 1:100, Invitrogen) was added dropwise on the surface of the tissue sections, and incubated overnight at 4°C. .. The next day, the tissue sections were incubated with FITC‐labeled goat anti‐rabbit IgG (F‐2765, 1:100, Invitrogen) for 1 h at 37°C away from light, and then they were exposed to DAPI stain (C1005, Beyotime) for 10 min, and observed using fluorescence microscopy. ..

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Article Title: Therapeutic potential of Platycodin D in allergic asthma through anti-inflammatory and anti-remodeling effects.
    Article Snippet: Background: Allergic asthma (AA) is a prevalent chronic respiratory disease characterized by airway hyperresponsiveness (AHR) and chronic inflammation, significantly impairing patients’ quality of life.. Purpose: This study investigates the therapeutic effects of Platycodin D (PLD) on AA and its underlying mechanisms via the EGFR/PI3K/Akt signaling pathway.. Methods: In vitro, BEAS-2B cells treated with IL-4 and IL-13 simulated asthma’s inflammatory environment.

    Article Title: Heterologous expression of AtLEC1 and AtLEC1-LIKE transcription factors redirects carbon flux toward lipid accumulation in diatom
    Article Snippet: .. The cell pellet was then treated with 150 μl of DAPI stain (Beyotime, C1006) and incubated for 10 min at ambient temperature. ..

    Article Title: Biodegradable Janus sonozyme with continuous reactive oxygen species regulation for treating infected critical-sized bone defects
    Article Snippet: .. The cells were covered with primary antibody of the appropriate genus and incubated at room temperature for 60 min, washed with 0.1% Phosphate Buffer Saline Tween (PBST), then DAPI stain (C1002, Beyotime) was added to the slides and incubated at room temperature for 10 min, protected from light. ..

    Article Title: Heterologous expression of AtLEC1 and AtLEC1-LIKE transcription factors redirects carbon flux toward lipid accumulation in diatom.
    Article Snippet: .. The cell pellet 175 was then treated with 150 μl of DAPI stain (Beyotime, C1006) and incubated 176 for 10 minutes at ambient temperature. ..

    Fluorescence:

    Article Title: Trans‐Coumaryl acetate mediates GRK5/NF‐κB/Nrf2 signaling axis to ameliorate septic acute kidney injury
    Article Snippet: Cell surfaces or tissue sections were permeabilized with drops of 0.3% Tritonx‐100 (X100, Sigma‐Aldrich) for 10 min 5% bovine serum albumin (BSA, V900933, Sigma‐Aldrich) was added for closure for 30 min. NF‐κB primary antibody (14‐6731‐81, 1:100, Invitrogen) was added dropwise on the cell surface, and F4/80 primary antibody (MA5‐16363, 1:100, Invitrogen) was added dropwise on the surface of the tissue sections, and incubated overnight at 4°C. .. The next day, the tissue sections were incubated with FITC‐labeled goat anti‐rabbit IgG (F‐2765, 1:100, Invitrogen) for 1 h at 37°C away from light, and then they were exposed to DAPI stain (C1005, Beyotime) for 10 min, and observed using fluorescence microscopy. ..

    Article Title: Therapeutic potential of Platycodin D in allergic asthma through anti-inflammatory and anti-remodeling effects.
    Article Snippet: Background: Allergic asthma (AA) is a prevalent chronic respiratory disease characterized by airway hyperresponsiveness (AHR) and chronic inflammation, significantly impairing patients’ quality of life.. Purpose: This study investigates the therapeutic effects of Platycodin D (PLD) on AA and its underlying mechanisms via the EGFR/PI3K/Akt signaling pathway.. Methods: In vitro, BEAS-2B cells treated with IL-4 and IL-13 simulated asthma’s inflammatory environment.

    Microscopy:

    Article Title: Trans‐Coumaryl acetate mediates GRK5/NF‐κB/Nrf2 signaling axis to ameliorate septic acute kidney injury
    Article Snippet: Cell surfaces or tissue sections were permeabilized with drops of 0.3% Tritonx‐100 (X100, Sigma‐Aldrich) for 10 min 5% bovine serum albumin (BSA, V900933, Sigma‐Aldrich) was added for closure for 30 min. NF‐κB primary antibody (14‐6731‐81, 1:100, Invitrogen) was added dropwise on the cell surface, and F4/80 primary antibody (MA5‐16363, 1:100, Invitrogen) was added dropwise on the surface of the tissue sections, and incubated overnight at 4°C. .. The next day, the tissue sections were incubated with FITC‐labeled goat anti‐rabbit IgG (F‐2765, 1:100, Invitrogen) for 1 h at 37°C away from light, and then they were exposed to DAPI stain (C1005, Beyotime) for 10 min, and observed using fluorescence microscopy. ..

    Modification:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    CCK-8 Assay:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Isolation:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    SYBR Green Assay:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Real-time Polymerase Chain Reaction:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Acid Assay:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Membrane:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Data-independent acquisition:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).

    Glutathione Assay:

    Article Title: Human umbilical cord mesenchymal stem cell -derived exosomes alleviated the toxic effects induced by lead on HK-2 cells via regulating the unfolded protein response.
    Article Snippet: .. Chemicals and reagents utilized in this study are listed below: Lead acetate (Pb(Ac)2, Aladdin, China), High-glucose dulbecco’s modified eagle medium (DMEM, Gibco, USA), Trypsin - EDTA (TE, Gibco, USA), Fetal bovine serum (FBS, Gibco, USA), Penicillin / streptomycin (Gibco, USA), Cell Counting Kit-8 (CCK-8, Abbkine, China), Trizol RNA isolation reagent (Invitrogen, USA), TransScript RT reagent kit (TransGen Biotech, China), SYBR Green qPCR Kit (Accurate Biology, China), Bestar® SybrGreen qPCR Mastermix (Accurate Biology, China), DAPI stain (BestBio, China), PKH67 fluorescent dye (BestBio, China), RIPA Buffer (Beyotime, China), Phenylmethanesulfonyl fluoride (PMSF, Beyotime, China), Bicinchoninic Acid Assay (BCA, Beyotime, China), Ethidium bromide (EB, Sigma, USA), Dimethyl Sulfoxide (DMSO,Sigma, USA), Polyvinylidene fluoride membrane (PVDF, Cobetter, China), Bip antibody (Wanlei, China), CHOP antibody (Wanlei, China), Phospho-perk (Thr982) antibody (Wanlei, China), Perk antibody (HuaBio, China), Bax antibody (Huabio, China), Bcl2 antibody (Abmart, China), GAPDH antibody (Proteintech, China), HRP-conjugated Goat Anti-Rabbit IgG (DIA-AN, China), Enhanced chemiluminescence reagents (ECL, Bestbio, China), Superoxide dismutase enzyme, Malondialdehyde, Glutathione assay kit (SOD/MDA/GSH, Beyotime, China), GSK2606414 (Aladdin, China), Annexin V - FITC Apoptosis Detection Kit (UElandy, China), and other commonly employed chemicals and reagents. .. In this study, human tubular epithelial cell line HK-2 and hucMSC were sourced from the American Type Culture Collection (ATCC).



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    Thermo Fisher dihydrochloride dapi staining
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    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. <t>Phalloidin/DAPI</t> staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.
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    Servicebio Inc dapi staining solution
    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. <t>Phalloidin/DAPI</t> staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.
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    Sangon Biotech dapi stain solution
    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. <t>Phalloidin/DAPI</t> staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.
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    10X Genomics diamidino 2 phenylindole dapi staining
    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. <t>Phalloidin/DAPI</t> staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.
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    Image Search Results


    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. Phalloidin/DAPI staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.

    Journal: Biomaterials and Biosystems

    Article Title: The influence of simulated microgravity on MG-63 osteoblast-like cells cultured on polymeric scaffold

    doi: 10.1016/j.bbiosy.2026.100137

    Figure Lengend Snippet: Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. Phalloidin/DAPI staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.

    Article Snippet: Cell culture evaluation was performed using AlamarBlue Cell Viability test (ThermoFisher), lactate dehydrogenase activity assay (LDH, Takara, Saint-Germain-en-Laye, France), ALP activity assay based on p-nitrophenol (Sigma Aldrich), calcein-AM and propidium iodide (PI) staining (Sigma Aldrich), Alexa Fluor 488 phalloidin and 4′,6-diamidino-2-phenylindole, dihydrochloride (DAPI) staining (ThermoFisher).

    Techniques: Staining, Cell Culture