si c jun sc Search Results


si c jun sc  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology si c jun sc
Si C Jun Sc, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/si+c+jun+sc/pmc07684958-44-6-17?v=Santa+Cruz+Biotechnology
Average 93 stars, based on 1 article reviews
si c jun sc - by Bioz Stars, 2026-07
93/100 stars
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sirna against c jun  (Santa Cruz Biotechnology)
95
Santa Cruz Biotechnology sirna against c jun
(A) Apoptotic cell deaths were lower in LX-2 cells transfected with siRNAs against c-Jun <t>(si-c-Jun1</t> and <t>si-c-Jun2)</t> compared with LX-2 cells transfected with <t>siRNA-control</t> (si-C) after incubation with conditioned media from HepG2 in the presence of MG132 (lower panel). Western blot analysis of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2 after 24 hours of MG132 treatment (upper panel). (B) Overexpression of c-Jun by the transfection of pMEKK into LX-2 cells enhanced apoptosis in LX-2 cells treated with conditioned media from HepG2.2.15 in the presence of MG132 (lower panel). Western blot analyses of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2.2.15 after 24 hours of MG132 treatment (upper panel). Apoptosis was quantified using the APOPercentage Apoptosis Assay. Data are expressed as mean ± standard deviations of triplicate determinations. (C) Conditioned media from HepG2.2.15 (2.2.15-CM) protects hepatic stellate cells from MG132-induced apoptosis and DNA damage. Confocal microscopic findings with a high-power view (x200) of the expression of phosphorylated histone H2AX (γ-H2AX) (red), a DNA damage marker, and Annexin V (green), an apoptosis marker, in LX-2 cells treated with conditioned media from HepG2.2.15 (upper panel) or HepG2 (lower panel) in the presence of MG132.
Sirna Against C Jun, supplied by Santa Cruz Biotechnology, 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/si+c+jun+sc/pmc04701422-71-1-14?v=Santa+Cruz+Biotechnology
Average 95 stars, based on 1 article reviews
sirna against c jun - by Bioz Stars, 2026-07
95/100 stars
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basic leucine zipper transcription factor atf-like 3 human recombinant  (Angio-Proteomie)
N/A
BATF3 Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 150 amino acids (1-127 a.a) and having a molecular mass of 16.9kDa. BATF3 is fused to a 23 amino acid His-tag at
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(A) Apoptotic cell deaths were lower in LX-2 cells transfected with siRNAs against c-Jun (si-c-Jun1 and si-c-Jun2) compared with LX-2 cells transfected with siRNA-control (si-C) after incubation with conditioned media from HepG2 in the presence of MG132 (lower panel). Western blot analysis of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2 after 24 hours of MG132 treatment (upper panel). (B) Overexpression of c-Jun by the transfection of pMEKK into LX-2 cells enhanced apoptosis in LX-2 cells treated with conditioned media from HepG2.2.15 in the presence of MG132 (lower panel). Western blot analyses of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2.2.15 after 24 hours of MG132 treatment (upper panel). Apoptosis was quantified using the APOPercentage Apoptosis Assay. Data are expressed as mean ± standard deviations of triplicate determinations. (C) Conditioned media from HepG2.2.15 (2.2.15-CM) protects hepatic stellate cells from MG132-induced apoptosis and DNA damage. Confocal microscopic findings with a high-power view (x200) of the expression of phosphorylated histone H2AX (γ-H2AX) (red), a DNA damage marker, and Annexin V (green), an apoptosis marker, in LX-2 cells treated with conditioned media from HepG2.2.15 (upper panel) or HepG2 (lower panel) in the presence of MG132.

Journal: PLoS ONE

Article Title: Possible Involvement of Hepatitis B Virus Infection of Hepatocytes in the Attenuation of Apoptosis in Hepatic Stellate Cells

doi: 10.1371/journal.pone.0146314

Figure Lengend Snippet: (A) Apoptotic cell deaths were lower in LX-2 cells transfected with siRNAs against c-Jun (si-c-Jun1 and si-c-Jun2) compared with LX-2 cells transfected with siRNA-control (si-C) after incubation with conditioned media from HepG2 in the presence of MG132 (lower panel). Western blot analysis of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2 after 24 hours of MG132 treatment (upper panel). (B) Overexpression of c-Jun by the transfection of pMEKK into LX-2 cells enhanced apoptosis in LX-2 cells treated with conditioned media from HepG2.2.15 in the presence of MG132 (lower panel). Western blot analyses of c-Jun and GAPDH expression in LX-2 cells treated with conditioned media from HepG2.2.15 after 24 hours of MG132 treatment (upper panel). Apoptosis was quantified using the APOPercentage Apoptosis Assay. Data are expressed as mean ± standard deviations of triplicate determinations. (C) Conditioned media from HepG2.2.15 (2.2.15-CM) protects hepatic stellate cells from MG132-induced apoptosis and DNA damage. Confocal microscopic findings with a high-power view (x200) of the expression of phosphorylated histone H2AX (γ-H2AX) (red), a DNA damage marker, and Annexin V (green), an apoptosis marker, in LX-2 cells treated with conditioned media from HepG2.2.15 (upper panel) or HepG2 (lower panel) in the presence of MG132.

Article Snippet: The siRNA against c-Jun (si-c-Jun1 and si-c-Jun2) and control siRNA (si-C) were obtained from Santa Cruz Biotechnology.

Techniques: Transfection, Control, Incubation, Western Blot, Expressing, Over Expression, Apoptosis Assay, Marker