nci h661 Search Results


95
ATCC nci h661
Nci H661, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nci+h661/NCI-H661/bio_rxiv__64898__2026__03__14__711762-160-4-5
Average 95 stars, based on 1 article reviews
nci h661 - by Bioz Stars, 2026-09
95/100 stars
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This product is a labeled stable pool in the designated cell type. This stable cell line expresses eGFP. This cell line can be used in vitro for cancer cell line research or in vivo to
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94
ATCC human h661 lung carcinoma cells
The Nox4 D loop facilitates interaction with p22phox Y121H. (A) <t>H661</t> cells coexpressing Nox4 with an empty vector (EV), wild-type p22phox, or p22phox Y121H were analyzed for H2O2 production (error bars indicate SDs; n = 3) and expression of Nox4 and p22phox proteins. Actin served as a loading control. (B) Maturation of Nox2 and chimeras 12a (upper panel) and chimeras 3b, 4b, and 5b (lower panel) to a 91-kDa form and p22phox expression were determined by immunoblotting. Actin served as a loading control. (C) Analysis of Nox4, Nox2, and chimera localization using immunofluorescence. Transfected H661 cells were stained with anti-Nox4 (red, first and third panels) or anti-Nox2 (green, second panel) and anti-p22phox (wild-type p22phox and p22phox Y121H, in green for panels 1 and 3 and in red for panel 2). All images displayed are merged pictures of all three channels, with white indicating regions of colocalization. Scale bars represent 20 μm.
Human H661 Lung Carcinoma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nci+h661/NCI-H661%3B+Lung+Carcinoma%3B+Human/pmc02815567-45-0-5
Average 94 stars, based on 1 article reviews
human h661 lung carcinoma cells - by Bioz Stars, 2026-09
94/100 stars
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90
iCell Bioscience Inc nci-h661
The Nox4 D loop facilitates interaction with p22phox Y121H. (A) <t>H661</t> cells coexpressing Nox4 with an empty vector (EV), wild-type p22phox, or p22phox Y121H were analyzed for H2O2 production (error bars indicate SDs; n = 3) and expression of Nox4 and p22phox proteins. Actin served as a loading control. (B) Maturation of Nox2 and chimeras 12a (upper panel) and chimeras 3b, 4b, and 5b (lower panel) to a 91-kDa form and p22phox expression were determined by immunoblotting. Actin served as a loading control. (C) Analysis of Nox4, Nox2, and chimera localization using immunofluorescence. Transfected H661 cells were stained with anti-Nox4 (red, first and third panels) or anti-Nox2 (green, second panel) and anti-p22phox (wild-type p22phox and p22phox Y121H, in green for panels 1 and 3 and in red for panel 2). All images displayed are merged pictures of all three channels, with white indicating regions of colocalization. Scale bars represent 20 μm.
Nci H661, supplied by iCell Bioscience Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nci+h661/nci+h661/pm36907878-53-0-9
Average 90 stars, based on 1 article reviews
nci-h661 - by Bioz Stars, 2026-09
90/100 stars
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This product is a cell line stably expressing the CRISPR Cas9 nuclease. This cell line also expresses the hygromycin resistance gene. In combination with separately transfected or transduced single guide RNAs (sgRNAs), this cell line
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NCI-H661 Cell Lines Complete Growth Medium is a cell lines complete growth medium from Innovative Research, supplied as a ready-to-use liquid. More Details: Formulation: RPMI-1640 + 10% FBS + 1% P/S Bacterial detection: Negative Fungal
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The NCI-H661 Luciferase cell line is transformed from NCI-H661 cell, expressing the firefly luciferase gene. The cell constitutively express Luciferase.
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N/A
This product is a dual-labeled stable pool in the designated cell type. This stable cell line expresses firefly luciferase and eGFP simultaneously. This cell line can be used in vitro for cancer cell line research
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Image Search Results


The Nox4 D loop facilitates interaction with p22phox Y121H. (A) H661 cells coexpressing Nox4 with an empty vector (EV), wild-type p22phox, or p22phox Y121H were analyzed for H2O2 production (error bars indicate SDs; n = 3) and expression of Nox4 and p22phox proteins. Actin served as a loading control. (B) Maturation of Nox2 and chimeras 12a (upper panel) and chimeras 3b, 4b, and 5b (lower panel) to a 91-kDa form and p22phox expression were determined by immunoblotting. Actin served as a loading control. (C) Analysis of Nox4, Nox2, and chimera localization using immunofluorescence. Transfected H661 cells were stained with anti-Nox4 (red, first and third panels) or anti-Nox2 (green, second panel) and anti-p22phox (wild-type p22phox and p22phox Y121H, in green for panels 1 and 3 and in red for panel 2). All images displayed are merged pictures of all three channels, with white indicating regions of colocalization. Scale bars represent 20 μm.

Journal: Molecular and Cellular Biology

Article Title: Structural Insights into Nox4 and Nox2: Motifs Involved in Function and Cellular Localization

doi: 10.1128/MCB.01393-09

Figure Lengend Snippet: The Nox4 D loop facilitates interaction with p22phox Y121H. (A) H661 cells coexpressing Nox4 with an empty vector (EV), wild-type p22phox, or p22phox Y121H were analyzed for H2O2 production (error bars indicate SDs; n = 3) and expression of Nox4 and p22phox proteins. Actin served as a loading control. (B) Maturation of Nox2 and chimeras 12a (upper panel) and chimeras 3b, 4b, and 5b (lower panel) to a 91-kDa form and p22phox expression were determined by immunoblotting. Actin served as a loading control. (C) Analysis of Nox4, Nox2, and chimera localization using immunofluorescence. Transfected H661 cells were stained with anti-Nox4 (red, first and third panels) or anti-Nox2 (green, second panel) and anti-p22phox (wild-type p22phox and p22phox Y121H, in green for panels 1 and 3 and in red for panel 2). All images displayed are merged pictures of all three channels, with white indicating regions of colocalization. Scale bars represent 20 μm.

Article Snippet: Human H661 lung carcinoma cells (ATCC HTB-183) were cultivated in RPMI 1640, and Cos-p22phox cells ( 36 ), Cos-phox cells ( 27 ), and Cos-Nox4/p22phox cells were cultivated in Dulbecco modified Eagle medium (DMEM).

Techniques: Plasmid Preparation, Expressing, Control, Western Blot, Immunofluorescence, Transfection, Staining