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k 562 gfp k562 cells  (ATCC)


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    Structured Review

    ATCC k 562 gfp k562 cells
    K 562 Gfp K562 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/k+562+gfp+k562+cells/K-562-GFP/pmc13083201-50-8-12
    Average 99 stars, based on 23 article reviews
    k 562 gfp k562 cells - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Cell Characterization:

    Article Title: A novel cultivation strategy to recover NK cell cytotoxicity
    Article Snippet: Brussels, Belgium) at a concentration of 2.5 × 10 5 cells/mL and was supplemented with IL-2 every second day without media exchange or addition. .. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1640 medium (RPMI; Gibco, Grand Island, NY, United States) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States). .. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Homogeneous shear distribution improves NK-92 cell cytotoxicity in a clinically relevant 2 L membrane-stirred bioreactor
    Article Snippet: Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States of America) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1,640 medium (RPMI; Gibco, Grand Island, NY, United States of America) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States of America).. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions.
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. AR TIC LE IN PR ES S ARTICLE IN PRESS To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.

    Membrane:

    Article Title: A novel cultivation strategy to recover NK cell cytotoxicity
    Article Snippet: Brussels, Belgium) at a concentration of 2.5 × 10 5 cells/mL and was supplemented with IL-2 every second day without media exchange or addition. .. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1640 medium (RPMI; Gibco, Grand Island, NY, United States) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States). .. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Homogeneous shear distribution improves NK-92 cell cytotoxicity in a clinically relevant 2 L membrane-stirred bioreactor
    Article Snippet: Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States of America) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1,640 medium (RPMI; Gibco, Grand Island, NY, United States of America) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States of America).. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions.
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. AR TIC LE IN PR ES S ARTICLE IN PRESS To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.

    Standard Deviation:

    Article Title: A novel cultivation strategy to recover NK cell cytotoxicity
    Article Snippet: Brussels, Belgium) at a concentration of 2.5 × 10 5 cells/mL and was supplemented with IL-2 every second day without media exchange or addition. .. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1640 medium (RPMI; Gibco, Grand Island, NY, United States) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States). .. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Homogeneous shear distribution improves NK-92 cell cytotoxicity in a clinically relevant 2 L membrane-stirred bioreactor
    Article Snippet: Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.Cells were seeded in T-25 flasks after thawing and then progressively expanded to T-175 flask size.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, VA, United States of America) were maintained at standard cultivation conditions in a Roswell Park Memorial Institute 1,640 medium (RPMI; Gibco, Grand Island, NY, United States of America) containing 5% heat-inactivated fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific, Waltham, MA, United States of America).. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL in T75 flasks.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1 × 10 6 cells/mL.

    Article Title: Cultivation strategy optimisation for NK-92 cell line expansion in static conditions.
    Article Snippet: When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.When the culture volume exceeded 5 mL or 10 mL, the culture flask size was altered to a horizontally positioned T-25 or T-75 flask (Starlab, Brussels, Belgium), respectively.. AR TIC LE IN PR ES S ARTICLE IN PRESS To assess the cytotoxicity of the NK-92 cells, K-562-GFP (K562) cells (CCL-243-GFP, American Type Culture Collection, Manassas, USA) were maintained at standard culturing conditions in RPMI medium containing 10% heat-inactivated FBS.. Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.Regular subculture of K562 cells was done at a seeding concentration of 1x106 cells/mL.



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