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apc conjugated anti human cd133 1 antibody  (Miltenyi Biotec)


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    Miltenyi Biotec apc conjugated anti human cd133 1 antibody
    Apc Conjugated Anti Human Cd133 1 Antibody, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1554 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/apc+anti+human+cd133+1/CD133%2F1+Antibody%2C+anti-human/10__1007_slash_s00018___026___06376___x-166-10-19
    Average 95 stars, based on 1554 article reviews
    apc conjugated anti human cd133 1 antibody - by Bioz Stars, 2026-10
    95/100 stars

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    Staining:

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Suspension:

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Article Title: Direct Conversion of Human Stem Cell-Derived Glial Progenitor Cells into GABAergic Interneurons
    Article Snippet: hESC-derived GPCs between day 188 and 304 were dissociated for 8 min in Accutase (StemPro, Thermo Fisher, Waltham, MA, USA) and resuspended to 1 million cell/mL in Miltenyi wash buffer (phosphate-buffered saline [PBS, Gibco, Thermo Fisher; Waltham, MA, USA] + 0.5% bovine serum albumin Fraction V [BSA, Gibco, Thermo Fisher, Waltham, MA, USA] + 2 μM EDTA + 0.05‰ Phenol Red [Sigma-Aldrich, St. Louis, MO, USA]). .. A total of 100 μL of cell suspension was aliquoted per flow cytometry tube and incubation with fluorochrome-labeled antibodies (PE anti-human CD140a, 1:10 [BD Biosciences, cat. no. 556002, Eysins, Switzerland]; APC anti-CD44, 1:500 [Miltenyi, cat. no. 130-095-177, Bergisch Gladbach, Germany]; APC anti-human CD133/1, 1:50 [Miltenyi, cat. no. 130-113-668, Bergisch Gladbach, Germany]; FITC anti-human SSEA-4, 1:20 [Biolegend, cat. no. 330410, San Diego, CA, USA] was performed for 15 min at 4 °C. .. Cells were washed once using Miltenyi wash buffer, centrifuged for 10 min at 200× g , and transferred to 5 mL polystyrene tubes with cell-strainer caps in DMEM/F12 (Gibco, Thermo Fisher, Waltham, MA, USA) + DNAse (Sigma-Aldrich, St. Louis, MO, USA).

    Incubation:

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Article Title: Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
    Article Snippet: Flow cytometry analysis and FACS sorting For flow cytometry analysis of the cells between D130-270, the cell clusters were dissociated for 8 min in Accutase (StemPro; Thermo Fisher) and resuspended to 1 million cell/ml in Miltenyi wash buffer (PBS + 0.5% BSA Fraction V + 2 μM EDTA + 0.05‰ Phenol Red). .. For each staining, 100 ul cell suspension was used and the cells were incubated with fluorophore-conjugated antibodies for 15 min at 4°C (PE anti-human CD140a, BD Biosciences, cat. no. 556002, 1:10; APC anti-CD44 (Miltenyi, cat. no. 130-095-177, 1:500); APC anti-human CD133/1, (Miltenyi, cat. no. 130-113-668, 1:50); FITC anti-human SSEA-4, Biolegends, cat. no. 330410, 1:20). .. Following the 15 min incubation with the antibodies, the cells were washed with Miltenyi wash buffer, centrifuged for 10 min at 200 x g and transferred to 5 ml polystyrene tubes with cell-strainer caps at a final density of around 400,000 cells/ml in DMEM/F12 + DNase.

    Article Title: Direct Conversion of Human Stem Cell-Derived Glial Progenitor Cells into GABAergic Interneurons
    Article Snippet: hESC-derived GPCs between day 188 and 304 were dissociated for 8 min in Accutase (StemPro, Thermo Fisher, Waltham, MA, USA) and resuspended to 1 million cell/mL in Miltenyi wash buffer (phosphate-buffered saline [PBS, Gibco, Thermo Fisher; Waltham, MA, USA] + 0.5% bovine serum albumin Fraction V [BSA, Gibco, Thermo Fisher, Waltham, MA, USA] + 2 μM EDTA + 0.05‰ Phenol Red [Sigma-Aldrich, St. Louis, MO, USA]). .. A total of 100 μL of cell suspension was aliquoted per flow cytometry tube and incubation with fluorochrome-labeled antibodies (PE anti-human CD140a, 1:10 [BD Biosciences, cat. no. 556002, Eysins, Switzerland]; APC anti-CD44, 1:500 [Miltenyi, cat. no. 130-095-177, Bergisch Gladbach, Germany]; APC anti-human CD133/1, 1:50 [Miltenyi, cat. no. 130-113-668, Bergisch Gladbach, Germany]; FITC anti-human SSEA-4, 1:20 [Biolegend, cat. no. 330410, San Diego, CA, USA] was performed for 15 min at 4 °C. .. Cells were washed once using Miltenyi wash buffer, centrifuged for 10 min at 200× g , and transferred to 5 mL polystyrene tubes with cell-strainer caps in DMEM/F12 (Gibco, Thermo Fisher, Waltham, MA, USA) + DNAse (Sigma-Aldrich, St. Louis, MO, USA).

    Article Title: A distinct lineage pathway drives parvalbumin chandelier cell fate in human interneuron reprogramming
    Article Snippet: Briefly, cells were mechanically detached and dissociated with Accutase (StemPro, Thermo Fisher Scientific; Waltham, MA, USA) for 8 min and were resuspended in Miltenyi wash buffer [phosphate-buffered saline (PBS), Gibco, Thermo Fisher Scientific; Waltham, MA, USA; 0.5% BSA Fraction V Gibco, Thermo Fisher Scientific; Waltham, MA, USA; 2 μM EDTA; and 0.05‰ (per mil) Phenol Red, Sigma-Aldrich, St. Louis, MO, USA] in a concentration of 1 × 10 6 cells/ml. .. This was followed by incubation with fluorochrome-conjugated antibodies [PE anti-human CD140a (BD Biosciences, catalog no. 556002, Eysins, Switzerland 1:10), APC anti-CD44 (Miltenyi, catalog no. 130-113-331, Bergisch Gladbach, Germany, 1:100), APC anti-human CD133/1 (Miltenyi, catalog no. 130-113-668, Bergisch Gladbach, Germany, 1:50), and FITC anti-human SSEA-4 (BioLegend, catalog no. 330410, Bergisch Gladbach, Germany, 1:20)] for 15 min at 4°C and washed in wash buffer for 10 min at 200 g . Subsequently, cells were transferred into prewet 5-ml polystyrene tubes with cell-strainer caps with propidium iodide (PI; Miltenyi, catalog no. 130-095-177, 1:500, Bergisch Gladbach, Germany) to exclude dead cells. .. A total of 10,000 events were analyzed on a FACSAria III sorter (BD Biosciences, Eysins, Switzerland).

    Article Title: Generating human parvalbumin interneurons through 3D glia reprogramming
    Article Snippet: Briefly, cells were mechanically detached and dissociated with Accutase (StemPro, Thermo Fisher; Waltham, MA, USA) for 8 min and were resuspended in Miltenyi wash buffer (PBS, Gibco, Thermo Fisher; Waltham, MA, USA; 0.5% BSA Fraction V Gibco, Thermo Fisher; Waltham, MA, USA; 2μM EDTA; 0.05‰ Phenol Red Sigma-Aldrich, St. Louis, MO, USA) in a concentration of 1×10 cells/ml. .. This was followed by incubation with fluorochrome-conjugated antibodies (PE anti-human CD140a, [BD Biosciences, cat. no. 556002, Eysins, Switzerland 1:10]; APC anti-CD44, [Miltenyi, cat. no. 130-113-331, Bergisch Gladbach, Germany, 1:100]; APC anti-human CD133/1[Miltenyi, cat. no. 130-113-668, Bergisch Gladbach, Germany, 1:50]; FITC anti-human SSEA-4, [Biolegends, cat. no. 330410, Bergisch Gladbach, Germany, 1:20]) for 15 min at 4°C and washed in wash buffer for 10 min at 200 x g. Subsequently, cells were transferred into pre-wet 5 ml polystyrene tubes with cell-strainer caps with propidium iodide (PI, Miltenyi, cat. no. 130-095-177, 1:500, Bergisch Gladbach, Germany) to exclude dead cells. .. 10.000 events were analyzed on a FACSAria III sorter (BD Biosciences, Eysins, Switzerland).

    Flow Cytometry:

    Article Title: Direct Conversion of Human Stem Cell-Derived Glial Progenitor Cells into GABAergic Interneurons
    Article Snippet: hESC-derived GPCs between day 188 and 304 were dissociated for 8 min in Accutase (StemPro, Thermo Fisher, Waltham, MA, USA) and resuspended to 1 million cell/mL in Miltenyi wash buffer (phosphate-buffered saline [PBS, Gibco, Thermo Fisher; Waltham, MA, USA] + 0.5% bovine serum albumin Fraction V [BSA, Gibco, Thermo Fisher, Waltham, MA, USA] + 2 μM EDTA + 0.05‰ Phenol Red [Sigma-Aldrich, St. Louis, MO, USA]). .. A total of 100 μL of cell suspension was aliquoted per flow cytometry tube and incubation with fluorochrome-labeled antibodies (PE anti-human CD140a, 1:10 [BD Biosciences, cat. no. 556002, Eysins, Switzerland]; APC anti-CD44, 1:500 [Miltenyi, cat. no. 130-095-177, Bergisch Gladbach, Germany]; APC anti-human CD133/1, 1:50 [Miltenyi, cat. no. 130-113-668, Bergisch Gladbach, Germany]; FITC anti-human SSEA-4, 1:20 [Biolegend, cat. no. 330410, San Diego, CA, USA] was performed for 15 min at 4 °C. .. Cells were washed once using Miltenyi wash buffer, centrifuged for 10 min at 200× g , and transferred to 5 mL polystyrene tubes with cell-strainer caps in DMEM/F12 (Gibco, Thermo Fisher, Waltham, MA, USA) + DNAse (Sigma-Aldrich, St. Louis, MO, USA).



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