jurkat atcc cat Search Results


99
ATCC cclv rie 0350 rrid cvcl c190 human jurkat
Cclv Rie 0350 Rrid Cvcl C190 Human Jurkat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC fas associated death domain fadd protein
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Fas Associated Death Domain Fadd Protein, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC jurkat atcc cat
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Jurkat Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC cell lines jurkat 76 mirjam heemskerk47 n a raji atcc
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Cell Lines Jurkat 76 Mirjam Heemskerk47 N A Raji Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
ATCC jurkat cells
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Jurkat Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DSMZ cell lines jurkat dsmz acc 282 hek293t atcc cat
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Cell Lines Jurkat Dsmz Acc 282 Hek293t Atcc Cat, supplied by DSMZ, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC cat tib 202 crl 1593 2
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Cat Tib 202 Crl 1593 2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
ATCC jurkat a3 permanent human t cell line
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Jurkat A3 Permanent Human T Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
ATCC jurkat male cells
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Jurkat Male Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC cell lines jurkat e6 1 atcc cat
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Cell Lines Jurkat E6 1 Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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98
ATCC tib 39 rrid cvcl 0255 llc1
( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN <t>FADD)</t> leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.
Tib 39 Rrid Cvcl 0255 Llc1, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN FADD) leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.

Journal: PLoS ONE

Article Title: Structurally simplified biphenyl combretastatin A4 derivatives retain in vitro anti-cancer activity dependent on mitotic arrest

doi: 10.1371/journal.pone.0171806

Figure Lengend Snippet: ( A) Wild-type E6-1 leukemia cells and dominant-negative Fas-associated via death domain (DN FADD) leukemia cells were treated with the indicated drug at the indicated dose for 48 hours and the WST-1 reagent was used to quantify proliferation. Absorbance was read at 450 nm and expressed as a % of DMSO control. (B, C) Cells were treated for either (B) 24 hours or (C) 48 hours and were probed with annexin V and propidium iodide (PI). Percentage of annexin V and PI positive cells was quantified using image-based cytometry. Blue bar represents viable cells; orange bar represents PI and annexin V positive cells; green bar represents annexin V positive cells; red bar represents PI positive cells. Values are expressed as mean ± SD from three independent experiments. * p < 0.05 vs. DMSO control; **** p < 0.0001 vs. DMSO control.

Article Snippet: E6-1 jurkat cells (ATCC, Cat. No. TIB-152, Manassas, VA, USA), an acute T-cell leukemia cell line, as well as a jurkat cell line dominant negative for the Fas-Associated Death Domain (FADD) protein (DN-FADD Jurkat; ATCC, Cat. No. CRL-2572, Manassas, VA, USA), were cultured with RPMI-1640 (Sigma-Aldrich Canada, Mississauga, ON, Canada) supplemented with 10% (v/v) FBS standard (Thermo Scientific, Waltham, MA, USA).

Techniques: Dominant Negative Mutation, Control, Cytometry