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apoptosis analysis kit  (Beyotime)


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    Beyotime apoptosis analysis kit
    Apoptosis Analysis Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 3191 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/apoptosis+analysis+kit/Cell+Cycle+and+Apoptosis+Analysis+Kit/pmc12963922-464-3-6
    Average 99 stars, based on 3191 article reviews
    apoptosis analysis kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Staining:

    Article Title: A photodynamically activated nanoplatform relieves glucose-driven immunosuppression to potentiate STING immunotherapy in triple-negative breast cancer
    Article Snippet: Pre-screened foetal bovine serum (FBP-C520) was procured from Haixing Biosciences. .. DAPI Staining Solution, Cell Viability/Cytotoxicity assay kit, Cell Cycle and Apoptosis analysis kit, Reactive Oxygen Species (ROS) assay kit, and Mitochondrial Membrane Potential assay kit with JC-1 were all purchased from Beyotime, Inc. .. Cell Counting Kit-8 was obtained from TargetMol, USA.

    Article Title: Comparative transcriptome analysis reveals the coordinated regulation of the miR-34c-5p/AASS axis in chicken skeletal muscle development and intramuscular fat deposition
    Article Snippet: .. For cell cycle analysis, CPMs and CIPs were fixed in 90 % ethanol at −20 °C overnight and stained with propidium iodide from the Cell Cycle and Apoptosis Analysis Kit (Beyotime, Beijing, China). .. The distribution of the cell cycle was assessed with an ABD Accuri C6 flow cytometer (BD Biosciences, San Jose, CA, USA) and analyzed using FlowJo software (Treestar Incorporated, Ashland, OR, USA).

    Article Title: Compound Platycladus orientalis tincture promotes hair regrowth and is associated with hair-cycle progression and Wnt/β-catenin-related signaling.
    Article Snippet: Ethnopharmacological relevance: Alopecia is traditionally managed in Chinese medicine using topical botanical preparations aimed at restoring hair-cycle dynamics and improving the follicular microenvironment.. Compound Platycladus orientalis tincture (CPT), an ethanol-based polyherbal formulation consisting of Platycladi Cacumen, Szechwan Chinaberry Fruit, and Herba Speranskiae Tuberculatae, has been used clinically as an in-hospital topical preparation for hair loss, yet its chemical basis and pharmacological mechanisms remain insufficiently defined.. Aim of the study: To characterize the chemical profile of CPT and to elucidate its efficacy, preliminary safety profile, and mechanistic basis in promoting hair regrowth in preclinical models of androgenetic alopecia (AGA) and cyclophosphamide-induced alopecia areata-like hair loss, with supporting cellular and network-level

    ROS Assay:

    Article Title: A photodynamically activated nanoplatform relieves glucose-driven immunosuppression to potentiate STING immunotherapy in triple-negative breast cancer
    Article Snippet: Pre-screened foetal bovine serum (FBP-C520) was procured from Haixing Biosciences. .. DAPI Staining Solution, Cell Viability/Cytotoxicity assay kit, Cell Cycle and Apoptosis analysis kit, Reactive Oxygen Species (ROS) assay kit, and Mitochondrial Membrane Potential assay kit with JC-1 were all purchased from Beyotime, Inc. .. Cell Counting Kit-8 was obtained from TargetMol, USA.

    Membrane:

    Article Title: A photodynamically activated nanoplatform relieves glucose-driven immunosuppression to potentiate STING immunotherapy in triple-negative breast cancer
    Article Snippet: Pre-screened foetal bovine serum (FBP-C520) was procured from Haixing Biosciences. .. DAPI Staining Solution, Cell Viability/Cytotoxicity assay kit, Cell Cycle and Apoptosis analysis kit, Reactive Oxygen Species (ROS) assay kit, and Mitochondrial Membrane Potential assay kit with JC-1 were all purchased from Beyotime, Inc. .. Cell Counting Kit-8 was obtained from TargetMol, USA.

    Cell Cycle Assay:

    Article Title: Comparative transcriptome analysis reveals the coordinated regulation of the miR-34c-5p/AASS axis in chicken skeletal muscle development and intramuscular fat deposition
    Article Snippet: .. For cell cycle analysis, CPMs and CIPs were fixed in 90 % ethanol at −20 °C overnight and stained with propidium iodide from the Cell Cycle and Apoptosis Analysis Kit (Beyotime, Beijing, China). .. The distribution of the cell cycle was assessed with an ABD Accuri C6 flow cytometer (BD Biosciences, San Jose, CA, USA) and analyzed using FlowJo software (Treestar Incorporated, Ashland, OR, USA).

    Analysis:

    Article Title: Isoprenylated phenolic derivatives from Corethrodendron scoparium and their anti-triple negative breast cancer activity.
    Article Snippet: Seventeen undescribed isoprenylated phenolics, including depsidones (1 and 2), depsides (3 and 4), stilbenoid (5), isoflavonoids (6–12), and flavonoids (13–17), together with thirteen known analogues (18–30), were isolated from the roots and stems of Corethrodendron scoparium (Fabaceae).. Structurally, compounds 1 and 2 possess an unprecedented isoprenylated depsidone framework, while compound 6 represents an unusual subtype of rearranged isoprenylated isoflavone.. Their structures were established by spectroscopic methods and chiral analysis.

    Flow Cytometry:

    Article Title: Compound Platycladus orientalis tincture promotes hair regrowth and is associated with hair-cycle progression and Wnt/β-catenin-related signaling.
    Article Snippet: Ethnopharmacological relevance: Alopecia is traditionally managed in Chinese medicine using topical botanical preparations aimed at restoring hair-cycle dynamics and improving the follicular microenvironment.. Compound Platycladus orientalis tincture (CPT), an ethanol-based polyherbal formulation consisting of Platycladi Cacumen, Szechwan Chinaberry Fruit, and Herba Speranskiae Tuberculatae, has been used clinically as an in-hospital topical preparation for hair loss, yet its chemical basis and pharmacological mechanisms remain insufficiently defined.. Aim of the study: To characterize the chemical profile of CPT and to elucidate its efficacy, preliminary safety profile, and mechanistic basis in promoting hair regrowth in preclinical models of androgenetic alopecia (AGA) and cyclophosphamide-induced alopecia areata-like hair loss, with supporting cellular and network-level



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    Broad-spectrum antitumor activity of B6ADC (A) Tumor suppression efficacy of B6ADC in multiple pancreatic cancer CDX models ( n = 5∼7/group). (B) Tumor suppression efficacy of B6ADC in four cell lines with varying TROP2/c-Met expression levels ( n = 5∼7/group). Scale bar, 50 μm. (C) Tumor suppression effect of a single 2.2 mg/kg dose of B6ADC in SPC-A1 lung adenocarcinoma-bearing mice with a tumor volume of 1,200 mm 3 ( n = 5∼7/group). (D) Comparison of tumor suppression between B6ADC and the combination of parental “TROP2ADC and c-MetADC” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 6/group). See also . (E) Comparison of tumor suppression between B6ADC and the combination of “marketed TROP2ADC (SG) and marketed c-MetADC (Teliso-V)” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 5∼7/group). See also . (F) Transmission electron microscopy images showing <t>apoptosis</t> in BxPC-3 tumors on day 7 after treatment with B6ADC and the control. Apoptotic features (e.g., chromatin condensation and nuclear fragmentation) were observed in the B6ADC-treated group ( n = 3 independent experiments). Scale bar, 2 μm. See also . Statistical analysis was performed using two-way ANOVA. The data are presented as the means ± SDs. ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and p > 0.05 (no significance, ns).
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    Beyotime beyotime cell cycle
    Broad-spectrum antitumor activity of B6ADC (A) Tumor suppression efficacy of B6ADC in multiple pancreatic cancer CDX models ( n = 5∼7/group). (B) Tumor suppression efficacy of B6ADC in four cell lines with varying TROP2/c-Met expression levels ( n = 5∼7/group). Scale bar, 50 μm. (C) Tumor suppression effect of a single 2.2 mg/kg dose of B6ADC in SPC-A1 lung adenocarcinoma-bearing mice with a tumor volume of 1,200 mm 3 ( n = 5∼7/group). (D) Comparison of tumor suppression between B6ADC and the combination of parental “TROP2ADC and c-MetADC” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 6/group). See also . (E) Comparison of tumor suppression between B6ADC and the combination of “marketed TROP2ADC (SG) and marketed c-MetADC (Teliso-V)” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 5∼7/group). See also . (F) Transmission electron microscopy images showing <t>apoptosis</t> in BxPC-3 tumors on day 7 after treatment with B6ADC and the control. Apoptotic features (e.g., chromatin condensation and nuclear fragmentation) were observed in the B6ADC-treated group ( n = 3 independent experiments). Scale bar, 2 μm. See also . Statistical analysis was performed using two-way ANOVA. The data are presented as the means ± SDs. ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and p > 0.05 (no significance, ns).
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    Image Search Results


    Broad-spectrum antitumor activity of B6ADC (A) Tumor suppression efficacy of B6ADC in multiple pancreatic cancer CDX models ( n = 5∼7/group). (B) Tumor suppression efficacy of B6ADC in four cell lines with varying TROP2/c-Met expression levels ( n = 5∼7/group). Scale bar, 50 μm. (C) Tumor suppression effect of a single 2.2 mg/kg dose of B6ADC in SPC-A1 lung adenocarcinoma-bearing mice with a tumor volume of 1,200 mm 3 ( n = 5∼7/group). (D) Comparison of tumor suppression between B6ADC and the combination of parental “TROP2ADC and c-MetADC” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 6/group). See also . (E) Comparison of tumor suppression between B6ADC and the combination of “marketed TROP2ADC (SG) and marketed c-MetADC (Teliso-V)” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 5∼7/group). See also . (F) Transmission electron microscopy images showing apoptosis in BxPC-3 tumors on day 7 after treatment with B6ADC and the control. Apoptotic features (e.g., chromatin condensation and nuclear fragmentation) were observed in the B6ADC-treated group ( n = 3 independent experiments). Scale bar, 2 μm. See also . Statistical analysis was performed using two-way ANOVA. The data are presented as the means ± SDs. ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and p > 0.05 (no significance, ns).

    Journal: Cell Reports Medicine

    Article Title: A bispecific nanobody-drug conjugate targeting TROP2 and c-Met for low-concentration, single-dose treatment of pancreatic cancer

    doi: 10.1016/j.xcrm.2026.102688

    Figure Lengend Snippet: Broad-spectrum antitumor activity of B6ADC (A) Tumor suppression efficacy of B6ADC in multiple pancreatic cancer CDX models ( n = 5∼7/group). (B) Tumor suppression efficacy of B6ADC in four cell lines with varying TROP2/c-Met expression levels ( n = 5∼7/group). Scale bar, 50 μm. (C) Tumor suppression effect of a single 2.2 mg/kg dose of B6ADC in SPC-A1 lung adenocarcinoma-bearing mice with a tumor volume of 1,200 mm 3 ( n = 5∼7/group). (D) Comparison of tumor suppression between B6ADC and the combination of parental “TROP2ADC and c-MetADC” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 6/group). See also . (E) Comparison of tumor suppression between B6ADC and the combination of “marketed TROP2ADC (SG) and marketed c-MetADC (Teliso-V)” in SPC-A1 tumor-bearing mice (initial tumor volume: 600 mm 3 ) ( n = 5∼7/group). See also . (F) Transmission electron microscopy images showing apoptosis in BxPC-3 tumors on day 7 after treatment with B6ADC and the control. Apoptotic features (e.g., chromatin condensation and nuclear fragmentation) were observed in the B6ADC-treated group ( n = 3 independent experiments). Scale bar, 2 μm. See also . Statistical analysis was performed using two-way ANOVA. The data are presented as the means ± SDs. ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and p > 0.05 (no significance, ns).

    Article Snippet: Cell Cycle and Apoptosis Analysis Kit , BEYOTIME , Cat#C1052.

    Techniques: Activity Assay, Expressing, Comparison, Transmission Assay, Electron Microscopy, Control