non adherent thp 1 cells Search Results


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ATCC non adherent human monocytic cell line
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DSMZ non adherent thp 1 cells
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ATCC human monocyte non adherent cell line thp 1 cells
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Federation of European Neuroscience Societies thp-1 cell
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Beijing CWBio trizol reagent (ultrapure rna kit
miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. <t>b</t> <t>THP-1</t> cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear <t>RNA</t> for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001
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Qiagen rneasy kit
miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. <t>b</t> <t>THP-1</t> cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear <t>RNA</t> for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001
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Thermo Fisher rna dna preparation thp 1 cells
miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. <t>b</t> <t>THP-1</t> cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear <t>RNA</t> for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001
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93
ATCC non hodgkin s lymphoma
miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. <t>b</t> <t>THP-1</t> cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear <t>RNA</t> for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001
Non Hodgkin S Lymphoma, 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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Image Search Results


miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. b THP-1 cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear RNA for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001

Journal: Journal of Nanobiotechnology

Article Title: SHED-derived exosomes promote LPS-induced wound healing with less itching by stimulating macrophage autophagy

doi: 10.1186/s12951-022-01446-1

Figure Lengend Snippet: miR-1246 as a SHED-Exo-enriched miRNA that stimulating macrophage autophagy. a The miRNA expression levels of SHED-derived exosomes were determined by qRT-PCR. Relative quantification was performed using cel-miR-39-3p for normalization. b THP-1 cells were incubated with 20 μg/mL SHED-Exo or transfected with 50 nM of miRNA mimics as indicated. The miR-1246, miR-100-5p, and miR-92a-3p levels were determined by qRT-PCR. Relative quantification was performed using U6 small nuclear RNA for normalization. c Gene expression levels of autophagy markers Lc3b in THP-1 macrophages per group. d THP-1 cells were transfected with 50 nM of miR-1246 mimic and 100 nM of miR-1246 inhibitor. Western blot results and relative expression levels of LC3, AKT, ERK1/2, and STAT3 signaling pathway proteins per treatment group. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001

Article Snippet: Mouse skin samples and THP-1 cells were homogenized using TRIzol reagent (Ultrapure RNA Kit, CW Biotech).

Techniques: Expressing, Derivative Assay, Quantitative RT-PCR, Incubation, Transfection, Western Blot