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buffer  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec buffer
    Buffer, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 96/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/binding+buffer/MACS+ART+Binding+Buffer/pmc06219306-62-30-35
    Average 96 stars, based on 3 article reviews
    buffer - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Human brain cell types shape host-rabies virus transcriptional interactions revealing a preexisting pro-viral astrocyte subpopulation
    Article Snippet: Samples were added to the freshly washed LS columns (130-042-401, Miltenyi Biotec). .. Columns were washed with 4.5 mL binding buffer (Miltenyi Biotec) and the flow-through was collected. ..

    Article Title: Transmembrane thiol isomerase TMX1 inhibits fibrin formation by down-regulation of platelet phosphatidylserine exposure
    Article Snippet: .. The cell pellet was suspended with 90 μl binding buffer per 10 7 total cells, followed by the addition of 10 μl CD31 MicroBeads (130–097–418, Miltenyi Biotec) per 10 7 total cells. .. After incubation at 4 °C for 15 min in the refrigerator, bead-bound (CD 31+ ) cells were collected by MACS magnetic separator and MS Column (130–042–2011; Miltenyi Biotec) according to the manufacturer’s protocol.

    Article Title: An optimised Bcl-3 inhibitor for melanoma treatment.
    Article Snippet: Input was saved before samples were incubated for 30 min at 4 C with rotation with GSTmicrobeads (130-091-370 kit, Miltenyi Biotec). μMACS columns (Miltenyi Biotec, Bergisch Gladbach, Germany) were placed in the separator and prepared with binding buffer. .. Samples were run through the columns and washed 2 with binding buffer, 2 with wash buffer 1, and 1 with wash buffer 2 before 20 μl pre-heated at 95 C elution buffer was added (all from 130-091-370 kit, Miltenyi Biotec), and eluates were collected before being subjected to Western blot analysis. .. Cells were transfected Flag-tagged Bcl-3 plasmid using Lipofectamine 2000 (Thermo Fisher Scientific) for 24 h. Cells were washed twice with PBS and collected using a lysis buffer consisting of 20 mM Tris– HCl (pH 7.6), 150 mM NaCl, 500 μM EDTA, Triton X-100, complemented with Sodium Orthovanadate, PMSF and complete protease inhibitors (Roche).

    Article Title: Human brain cell types shape host-rabies virus transcriptional interactions revealing a preexisting pro-viral astrocyte subpopulation.
    Article Snippet: Samples were added to the freshly washed LS columns (130-042-401, Miltenyi Biotec). .. Columns were washed with 4.5 mL binding buffer (Miltenyi Biotec) and the flow-through was collected. ..

    Article Title: Monocyte and macrophage binding aptamers and their application
    Article Snippet: Binding buffer: wash buffer+0.5% BSA (Miltenyi)+0.1 mg/mL tRNA (Invitrogen) *Avoid EDTA in the system .. Binding buffer: wash buffer+0.5% BSA (Miltenyi)+0.1 mg/mL tRNA (Invitrogen) *Avoid EDTA in the system ..

    Article Title: Functional phenotyping of genomic variants using joint multiomic single-cell DNA-RNA sequencing.
    Article Snippet: Cells were resuspended in 100 μl of bead solution from a Dead Cell Removal kit (Miltenyi Biotec, 130-090- 101) and incubated for 15 min in the dark. .. Binding buffer was prepared according to the manufacturer’s protocol, and the LS column (Miltenyi Biotec, 130-042-401) was washed with 500 μl of binding buffer. ..

    Article Title: Transmembrane thiol isomerase TMX1 inhibits fibrin formation by down-regulation of platelet phosphatidylserine exposure.
    Article Snippet: .. The cell pellet was suspended with 90 μl binding buffer per 107 total cells, followed by the addition of 10 μl CD31 MicroBeads (130–097–418, Miltenyi Biotec) per 107 total cells. .. After incubation at 4 °C for 15 min in the refrigerator, beadbound (CD31+) cells were collected by MACS magnetic separator and MS Column (130–042–2011; Miltenyi Biotec) according to the manufacturer’s protocol.

    Western Blot:

    Article Title: An optimised Bcl-3 inhibitor for melanoma treatment.
    Article Snippet: Input was saved before samples were incubated for 30 min at 4 C with rotation with GSTmicrobeads (130-091-370 kit, Miltenyi Biotec). μMACS columns (Miltenyi Biotec, Bergisch Gladbach, Germany) were placed in the separator and prepared with binding buffer. .. Samples were run through the columns and washed 2 with binding buffer, 2 with wash buffer 1, and 1 with wash buffer 2 before 20 μl pre-heated at 95 C elution buffer was added (all from 130-091-370 kit, Miltenyi Biotec), and eluates were collected before being subjected to Western blot analysis. .. Cells were transfected Flag-tagged Bcl-3 plasmid using Lipofectamine 2000 (Thermo Fisher Scientific) for 24 h. Cells were washed twice with PBS and collected using a lysis buffer consisting of 20 mM Tris– HCl (pH 7.6), 150 mM NaCl, 500 μM EDTA, Triton X-100, complemented with Sodium Orthovanadate, PMSF and complete protease inhibitors (Roche).

    other:

    Article Title: Unveiling IRF4-steered regulation of context-dependent effector programs in CD4 + T cells under Th17- and Treg-skewing conditions.
    Article Snippet: 24 Cell Reports 44, 115407, March 25, 2025 anti-CD44 (BioLegend).



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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