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binding buffer  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology binding buffer
    Binding Buffer, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 95 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/binding+buffer/Annexin+V+Binding+Buffer/pm41371635-58-8-22
    Average 95 stars, based on 95 article reviews
    binding buffer - by Bioz Stars, 2026-09
    95/100 stars

    Images

    Related Articles

    Binding Assay:

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: To assess necroptosis, RIPK3-OE NIH3T3 were induced by adding 30ng/ml TNF-α (SinoBiological, 50349-MNAE), 10uM Lcl-161 (MCE, HY-15518) and 100uM z-VAD-fmk (APExBIO, A1902) (TSZ) for indicated times. .. Then, cells were trypsinized, resuspended in Annexin V binding buffer and stained with Annexin V-APC (1:200, Elabscience, E-CKAR TI CL E IN P RE SS ARTICLE IN PRESS A117), 50 nM Sytox Green (Invitrogen, S7020) for 5min. .. Cells with Annexin V/ or Sytox Green/ were analysed by flow cytometry using CytoFLEX LX (Beckman Coulter).

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: .. Then, cells were trypsinized, resuspended in Annexin V binding buffer and stained with Annexin V-APC (1:200, Elabscience, E-CK- AR TI CL E IN P RE SS A117), 50 nM Sytox Green (Invitrogen, S7020) for 5min. .. Cells with Annexin V+/- or Sytox Green+/- were analysed by flow cytometry using CytoFLEX LX (Beckman Coulter).

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: .. After centrifugation and one wash with PBS, the cells were resuspended in Annexin V binding buffer and stained with Annexin V–APC (1:200, Elabscience) and 50 nM Sytox Green (Invitrogen) for 5 min. ..

    Article Title: An extracellular vesicle-mediated mitochondrial transfer network critical for testosterone synthesis
    Article Snippet: .. The tissues were incubated with Annexin V–APC (Elabscience) in Annexin binding buffer (10 mM HEPES–NaOH pH 7.4, 140 mM NaCl and 2.5 mM CaCl 2 ). ..

    Article Title: Network toxicology and single-cell analysis reveal key gene-mediated bisphenol a interference with granulosa cell function in polycystic ovary syndrome
    Article Snippet: .. Cells were centrifuged at 1000 rpm for 5 min, resuspended in 500 μL 1× Binding Buffer, and stained with 5 μL Annexin V-APC and 10 μL PI (Elabsciences, Wuhan) for 5 min at room temperature in the dark. ..

    Article Title: An extracellular vesicle-mediated mitochondrial transfer network critical for testosterone synthesis.
    Article Snippet: Testosterone production by testicular Leydig cells (LCs) in male mammals is energetically demanding and prone to mitochondrial damage.. Despite these challenges, LCs exhibit remarkable longevity and minimal turnover, suggesting the existence of specialized mechanisms that maintain LC mitochondrial homeostasis under such constrains.. Here we identify a mitochondrial transfer network between LCs and different testicular macrophage (tMac) subpopulations.

    Article Title: Identification and Functional Validation of PTH2R as a Therapeutic Target in Lung Adenocarcinoma.
    Article Snippet: After treatment, the cells were collected by centrifugation at 500 rpm for five minutes and washed twice with 1× phosphate buffer solution (PBS, Servicebio, China). .. The cells were reconstituted in 125 μL of 1× binding buffer supplemented with 1.25 μL each of APC-labeled Annexin V and DAPI (Elabscience, Wuhan, China)) added. ..

    Article Title: Identification and Functional Validation of PTH2R as a Therapeutic Target in Lung Adenocarcinoma
    Article Snippet: After treatment, the cells were collected by centrifugation at 500 rpm for five minutes and washed twice with 1× phosphate buffer solution (PBS, Servicebio, China). .. The cells were reconstituted in 125 μL of 1× binding buffer supplemented with 1.25 μL each of APC-labeled Annexin V and DAPI (Elabscience, Wuhan, China)) added. ..

    Staining:

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: To assess necroptosis, RIPK3-OE NIH3T3 were induced by adding 30ng/ml TNF-α (SinoBiological, 50349-MNAE), 10uM Lcl-161 (MCE, HY-15518) and 100uM z-VAD-fmk (APExBIO, A1902) (TSZ) for indicated times. .. Then, cells were trypsinized, resuspended in Annexin V binding buffer and stained with Annexin V-APC (1:200, Elabscience, E-CKAR TI CL E IN P RE SS ARTICLE IN PRESS A117), 50 nM Sytox Green (Invitrogen, S7020) for 5min. .. Cells with Annexin V/ or Sytox Green/ were analysed by flow cytometry using CytoFLEX LX (Beckman Coulter).

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: .. Then, cells were trypsinized, resuspended in Annexin V binding buffer and stained with Annexin V-APC (1:200, Elabscience, E-CK- AR TI CL E IN P RE SS A117), 50 nM Sytox Green (Invitrogen, S7020) for 5min. .. Cells with Annexin V+/- or Sytox Green+/- were analysed by flow cytometry using CytoFLEX LX (Beckman Coulter).

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: .. After centrifugation and one wash with PBS, the cells were resuspended in Annexin V binding buffer and stained with Annexin V–APC (1:200, Elabscience) and 50 nM Sytox Green (Invitrogen) for 5 min. ..

    Article Title: Network toxicology and single-cell analysis reveal key gene-mediated bisphenol a interference with granulosa cell function in polycystic ovary syndrome
    Article Snippet: .. Cells were centrifuged at 1000 rpm for 5 min, resuspended in 500 μL 1× Binding Buffer, and stained with 5 μL Annexin V-APC and 10 μL PI (Elabsciences, Wuhan) for 5 min at room temperature in the dark. ..

    Centrifugation:

    Article Title: Agonal cell resuscitation strategy to promote tissue repair.
    Article Snippet: .. After centrifugation and one wash with PBS, the cells were resuspended in Annexin V binding buffer and stained with Annexin V–APC (1:200, Elabscience) and 50 nM Sytox Green (Invitrogen) for 5 min. ..

    Incubation:

    Article Title: An extracellular vesicle-mediated mitochondrial transfer network critical for testosterone synthesis
    Article Snippet: .. The tissues were incubated with Annexin V–APC (Elabscience) in Annexin binding buffer (10 mM HEPES–NaOH pH 7.4, 140 mM NaCl and 2.5 mM CaCl 2 ). ..

    Article Title: An extracellular vesicle-mediated mitochondrial transfer network critical for testosterone synthesis.
    Article Snippet: Testosterone production by testicular Leydig cells (LCs) in male mammals is energetically demanding and prone to mitochondrial damage.. Despite these challenges, LCs exhibit remarkable longevity and minimal turnover, suggesting the existence of specialized mechanisms that maintain LC mitochondrial homeostasis under such constrains.. Here we identify a mitochondrial transfer network between LCs and different testicular macrophage (tMac) subpopulations.



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    CRISPR/Cas9 induces DNA damage and apoptosis in PGCs. (A) Flow cytometry analysis 24 h after electroporation, quantifying the proportion of <t>Annexin</t> <t>V</t> + /PI + cells. The horizontal axis indicates PI and the vertical axis Annexin V. The upper-left quadrant (Annexin V + /PI + ) represents late apoptotic cells, and the lower-right quadrant (Annexin V + only) represents early apoptotic cells. Upper panels: results after electroporation with Cas9 + various gRNAs; lower panels: results with dCas9 + various gRNAs. (B) Bar graph of Annexin V + /PI + percentages across groups. Cas9 editing induced a highly significant increase in late apoptosis. (C) γ-H 2 AX foci (green) detected by immunofluorescence 24 h after electroporation. Foci appear as discrete nuclear puncta; nuclei are counterstained with DAPI (blue). Scale bar = 10 µm. (D) Quantification of γ-H 2 AX foci per cell. Cas9 targeting resulted in a significant increase in γ-H 2 AX foci per cell, whereas dCas9 with sgRNA did not. Statistical significance determined by one-way ANOVA (p-values are indicated in the figure).
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    CRISPR/Cas9 induces DNA damage and apoptosis in PGCs. (A) Flow cytometry analysis 24 h after electroporation, quantifying the proportion of <t>Annexin</t> <t>V</t> + /PI + cells. The horizontal axis indicates PI and the vertical axis Annexin V. The upper-left quadrant (Annexin V + /PI + ) represents late apoptotic cells, and the lower-right quadrant (Annexin V + only) represents early apoptotic cells. Upper panels: results after electroporation with Cas9 + various gRNAs; lower panels: results with dCas9 + various gRNAs. (B) Bar graph of Annexin V + /PI + percentages across groups. Cas9 editing induced a highly significant increase in late apoptosis. (C) γ-H 2 AX foci (green) detected by immunofluorescence 24 h after electroporation. Foci appear as discrete nuclear puncta; nuclei are counterstained with DAPI (blue). Scale bar = 10 µm. (D) Quantification of γ-H 2 AX foci per cell. Cas9 targeting resulted in a significant increase in γ-H 2 AX foci per cell, whereas dCas9 with sgRNA did not. Statistical significance determined by one-way ANOVA (p-values are indicated in the figure).
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    Image Search Results


    CRISPR/Cas9 induces DNA damage and apoptosis in PGCs. (A) Flow cytometry analysis 24 h after electroporation, quantifying the proportion of Annexin V + /PI + cells. The horizontal axis indicates PI and the vertical axis Annexin V. The upper-left quadrant (Annexin V + /PI + ) represents late apoptotic cells, and the lower-right quadrant (Annexin V + only) represents early apoptotic cells. Upper panels: results after electroporation with Cas9 + various gRNAs; lower panels: results with dCas9 + various gRNAs. (B) Bar graph of Annexin V + /PI + percentages across groups. Cas9 editing induced a highly significant increase in late apoptosis. (C) γ-H 2 AX foci (green) detected by immunofluorescence 24 h after electroporation. Foci appear as discrete nuclear puncta; nuclei are counterstained with DAPI (blue). Scale bar = 10 µm. (D) Quantification of γ-H 2 AX foci per cell. Cas9 targeting resulted in a significant increase in γ-H 2 AX foci per cell, whereas dCas9 with sgRNA did not. Statistical significance determined by one-way ANOVA (p-values are indicated in the figure).

    Journal: Poultry Science

    Article Title: High genotoxicity of CRISPR/Cas9 versus limited efficacy of CRISPRi in chicken primordial germ cells

    doi: 10.1016/j.psj.2026.106722

    Figure Lengend Snippet: CRISPR/Cas9 induces DNA damage and apoptosis in PGCs. (A) Flow cytometry analysis 24 h after electroporation, quantifying the proportion of Annexin V + /PI + cells. The horizontal axis indicates PI and the vertical axis Annexin V. The upper-left quadrant (Annexin V + /PI + ) represents late apoptotic cells, and the lower-right quadrant (Annexin V + only) represents early apoptotic cells. Upper panels: results after electroporation with Cas9 + various gRNAs; lower panels: results with dCas9 + various gRNAs. (B) Bar graph of Annexin V + /PI + percentages across groups. Cas9 editing induced a highly significant increase in late apoptosis. (C) γ-H 2 AX foci (green) detected by immunofluorescence 24 h after electroporation. Foci appear as discrete nuclear puncta; nuclei are counterstained with DAPI (blue). Scale bar = 10 µm. (D) Quantification of γ-H 2 AX foci per cell. Cas9 targeting resulted in a significant increase in γ-H 2 AX foci per cell, whereas dCas9 with sgRNA did not. Statistical significance determined by one-way ANOVA (p-values are indicated in the figure).

    Article Snippet: After another centrifugation, the supernatant was removed and cells were resuspended in 500 μL of 1× Annexin V Binding Buffer (from Annexin V-FITC/PI Apoptosis Kit, Elabscience E-CK-A211).

    Techniques: CRISPR, Flow Cytometry, Electroporation, Immunofluorescence

    PGCs are more sensitive to DNA double-strand breaks than somatic cells. (A) Cell viability curves after 24 h treatment with increasing concentrations of etoposide (ETP; x-axis shows log 10 [ETP]). PGC viability dropped sharply even at low ETP doses, whereas CEF cells were more tolerant (viability data are mean ± SD of triplicates). (B) Apoptosis detection in PGCs treated with low-dose ETP. The proportion of Annexin V + /PI + cells (late apoptosis) was significantly elevated even at 0.03 µM ETP. (C) Western blot analysis of γ-H 2 AX protein in PGCs treated with varying ETP concentrations (left panel; β-actin as loading control). The bar graph (right) shows the ratio of γ-H 2 AX to β-actin band intensity, with a marked increase at 3 µM ETP (p-values are indicated in the figure). (D) Quantification of γ-H 2 AX foci per cell in THP-1 cells, male PGCs, and female PGCs after exposure to X-ray doses of 0, 2, 4, 6, and 8 Gy. After 48 h recovery, γ-H 2 AX foci increased significantly with higher radiation in THP-1, male PGCs, and female PGCs. Female PGC data points are red squares; male PGCs are blue squares; THP-1 are black circles. (E) Cell-cycle distribution of male vs. female PGCs after DNA damage. PGCs were irradiated (2, 4, 6 Gy), cultured 48 h, and analyzed by flow cytometry for cell-cycle phase (propidium iodide staining). Stacked bars show the percentage of cells in G 0 G 1 , S, and G 2 /M phases in untreated vs. irradiated cells. After damage, female PGCs predominantly arrested in G 2 /M (increased G 2 fraction), whereas male PGCs accumulated in S phase. Statistical significance by one-way ANOVA (p-values are indicated in the figure).

    Journal: Poultry Science

    Article Title: High genotoxicity of CRISPR/Cas9 versus limited efficacy of CRISPRi in chicken primordial germ cells

    doi: 10.1016/j.psj.2026.106722

    Figure Lengend Snippet: PGCs are more sensitive to DNA double-strand breaks than somatic cells. (A) Cell viability curves after 24 h treatment with increasing concentrations of etoposide (ETP; x-axis shows log 10 [ETP]). PGC viability dropped sharply even at low ETP doses, whereas CEF cells were more tolerant (viability data are mean ± SD of triplicates). (B) Apoptosis detection in PGCs treated with low-dose ETP. The proportion of Annexin V + /PI + cells (late apoptosis) was significantly elevated even at 0.03 µM ETP. (C) Western blot analysis of γ-H 2 AX protein in PGCs treated with varying ETP concentrations (left panel; β-actin as loading control). The bar graph (right) shows the ratio of γ-H 2 AX to β-actin band intensity, with a marked increase at 3 µM ETP (p-values are indicated in the figure). (D) Quantification of γ-H 2 AX foci per cell in THP-1 cells, male PGCs, and female PGCs after exposure to X-ray doses of 0, 2, 4, 6, and 8 Gy. After 48 h recovery, γ-H 2 AX foci increased significantly with higher radiation in THP-1, male PGCs, and female PGCs. Female PGC data points are red squares; male PGCs are blue squares; THP-1 are black circles. (E) Cell-cycle distribution of male vs. female PGCs after DNA damage. PGCs were irradiated (2, 4, 6 Gy), cultured 48 h, and analyzed by flow cytometry for cell-cycle phase (propidium iodide staining). Stacked bars show the percentage of cells in G 0 G 1 , S, and G 2 /M phases in untreated vs. irradiated cells. After damage, female PGCs predominantly arrested in G 2 /M (increased G 2 fraction), whereas male PGCs accumulated in S phase. Statistical significance by one-way ANOVA (p-values are indicated in the figure).

    Article Snippet: After another centrifugation, the supernatant was removed and cells were resuspended in 500 μL of 1× Annexin V Binding Buffer (from Annexin V-FITC/PI Apoptosis Kit, Elabscience E-CK-A211).

    Techniques: Western Blot, Control, Irradiation, Cell Culture, Flow Cytometry, Staining