origin cell Search Results


93
ATCC neural progenitor cell origin atcc bxs0117 normal
Neural Progenitor Cell Origin Atcc Bxs0117 Normal, 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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Chem Impex International glycerol chem impex
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Chem Impex International recombinant proteins 2
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JCRB Cell Bank fibroblast cell lines originating from human fetal lung tissue
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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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Average 90 stars, based on 1 article reviews
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90
Florman Family Foundation unresectable squamous cell carcinoma of donor origin
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.
Unresectable Squamous Cell Carcinoma Of Donor Origin, supplied by Florman Family Foundation, 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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Nokia Corporation battery of nokia n73
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.
Battery Of Nokia N73, supplied by Nokia Corporation, 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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HTG Molecular gep htg edgeseq dlbcl cell of origin assay
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.
Gep Htg Edgeseq Dlbcl Cell Of Origin Assay, supplied by HTG Molecular, 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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Cellomics Technology LLC hela-originated 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.
Hela Originated Cell Line, supplied by Cellomics Technology LLC, 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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90
Coriell Institute for Medical Research cell line repository
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.
Cell Line Repository, supplied by Coriell Institute for Medical Research, 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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90
Verlag GmbH origin and continuity of cell organelles
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.
Origin And Continuity Of Cell Organelles, supplied by Verlag GmbH, 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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90
Inserm Transfert m5-t1 original neoplastic 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.
M5 T1 Original Neoplastic Cell Line, supplied by Inserm Transfert, 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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m5-t1 original neoplastic cell line - by Bioz Stars, 2026-04
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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