raw264 7 mouse macrophages Search Results


90
Elabscience Biotechnology raw 264.7 mouse macrophages ep-cl-0190
Raw 264.7 Mouse Macrophages Ep Cl 0190, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pro-cell Co Ltd bv2 microglial cell line
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
Bv2 Microglial Cell Line, supplied by Pro-cell Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Viromer Transfection mouse monocyte/macrophage cell line raw264.7
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
Mouse Monocyte/Macrophage Cell Line Raw264.7, supplied by Viromer Transfection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Dawley Inc raw 264.7 murine cell
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
Raw 264.7 Murine Cell, supplied by Dawley Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Xiehe Group j774a.1 cells
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
J774a.1 Cells, supplied by Xiehe Group, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SAS institute mouse peritoneal macrophage cell line raw 264.7
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
Mouse Peritoneal Macrophage Cell Line Raw 264.7, supplied by SAS institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Beijing Xiehe Pharmaceutical Co Ltd mouse mono macrophage raw264.7 cells
A Immunoblot analysis of phosphorylated eIF2α in <t>BV2</t> cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.
Mouse Mono Macrophage Raw264.7 Cells, supplied by Beijing Xiehe Pharmaceutical Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Shanghai Genechem Ltd gfp (anti‑puromycin)-labeled raw 264.7 cell lines
The hybrid cell fusion by SCC7 and RAW 264.7 cells. (A) The diagram of the cell fusion process. (B) Immunofluorescence images of <t>Puro‐GFP‐RAW</t> <t>264.7,</t> <t>Neo‐mCherry‐SCC7</t> and hybrid cells. (C) DNA content. (D) Expression of CD163 and pan‐CK in RAW 264.7, SCC7, and hybrid cells. * p < 0.05, ** p < 0.01, *** p < 0.001.
Gfp (Anti‑Puromycin) Labeled Raw 264.7 Cell Lines, supplied by Shanghai Genechem Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Rochen Pharma Co Ltd mouse macrophage cell line raw 264.7
The hybrid cell fusion by SCC7 and RAW 264.7 cells. (A) The diagram of the cell fusion process. (B) Immunofluorescence images of <t>Puro‐GFP‐RAW</t> <t>264.7,</t> <t>Neo‐mCherry‐SCC7</t> and hybrid cells. (C) DNA content. (D) Expression of CD163 and pan‐CK in RAW 264.7, SCC7, and hybrid cells. * p < 0.05, ** p < 0.01, *** p < 0.001.
Mouse Macrophage Cell Line Raw 264.7, supplied by Rochen Pharma Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Hanlim Pharm Co mouse macrophage cell line raw 264.7
Inhibitory efficacies of AL and BAL on NO production in LPS-induced <t> macrophage </t> RAW 264.7 cells
Mouse Macrophage Cell Line Raw 264.7, supplied by Hanlim Pharm Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MatTek raw 264.7 mouse macrophage cells
Inhibitory efficacies of AL and BAL on NO production in LPS-induced <t> macrophage </t> RAW 264.7 cells
Raw 264.7 Mouse Macrophage Cells, supplied by MatTek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Eton Bioscience mouse leukemic monocyte macrophage cell line raw264.7
Inhibitory efficacies of AL and BAL on NO production in LPS-induced <t> macrophage </t> RAW 264.7 cells
Mouse Leukemic Monocyte Macrophage Cell Line Raw264.7, supplied by Eton Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


A Immunoblot analysis of phosphorylated eIF2α in BV2 cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.

Journal: EMBO Reports

Article Title: FAM69C functions as a kinase for eIF2α and promotes stress granule assembly

doi: 10.15252/embr.202255641

Figure Lengend Snippet: A Immunoblot analysis of phosphorylated eIF2α in BV2 cells. Primed (1 μg/ml LPS for 3 h) or unprimed BV2 cells were treated with mock, 5 mM ATP or 20 μM nigericin for 40 min, and lysates were immunoblotted with p‐eIF2α (S51) antibody. Representative blots, n = 3 biologically independent experiments. B Quantitative analysis of the phosphorylation level of eIF2α normalized with total eIF2α. ** P value < 0.01, paired two‐tailed t ‐test, n = 3 biologically independent experiments. Mean ± SD. For ATP versus mock, P value = 0.0047; For LPS + ATP versus LPS, P value = 0.0011.

Article Snippet: The BV2 microglial cell line was purchased from Procell Co., Ltd. and has been authenticated recently (#CL‐0493, Wuhan, China).

Techniques: Western Blot, Two Tailed Test

The hybrid cell fusion by SCC7 and RAW 264.7 cells. (A) The diagram of the cell fusion process. (B) Immunofluorescence images of Puro‐GFP‐RAW 264.7, Neo‐mCherry‐SCC7 and hybrid cells. (C) DNA content. (D) Expression of CD163 and pan‐CK in RAW 264.7, SCC7, and hybrid cells. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Cancer Medicine

Article Title: Cell fusion between tumor cells and macrophages promotes the metastasis of OSCC patient through the activation of the chemokine signaling pathway

doi: 10.1002/cam4.6940

Figure Lengend Snippet: The hybrid cell fusion by SCC7 and RAW 264.7 cells. (A) The diagram of the cell fusion process. (B) Immunofluorescence images of Puro‐GFP‐RAW 264.7, Neo‐mCherry‐SCC7 and hybrid cells. (C) DNA content. (D) Expression of CD163 and pan‐CK in RAW 264.7, SCC7, and hybrid cells. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Before cell fusion, mCherry (anti‐neomycin)‐labeled SCC7 cell lines and GFP (anti‐puromycin)‐labeled RAW 264.7 cell lines were generated by lentiviral infection (Shanghai GeneChem Co., Ltd).

Techniques: Immunofluorescence, Expressing

Inhibitory efficacies of AL and BAL on NO production in LPS-induced  macrophage  RAW 264.7 cells

Journal: Journal of Pharmacopuncture

Article Title: An Experimental Study of the Anti-oxidant and the Anti-inflammatory Effects of Alum and Burnt Alum

doi: 10.3831/KPI.2012.15.2.011

Figure Lengend Snippet: Inhibitory efficacies of AL and BAL on NO production in LPS-induced macrophage RAW 264.7 cells

Article Snippet: The human keratinocyte cell line (HaCaT) used for measuring the cytotoxicity was cultured in the Biochemistry Department of Gangwon University, and the mouse macrophage cell line (RAW 264.7) for measuring the anti-inflammatory effects was obtained from Technology Innovation Center of Hanlim University.

Techniques: