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anti lamin  (Developmental Studies Hybridoma Bank)
97
Developmental Studies Hybridoma Bank anti lamin
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Anti Lamin, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti lamin a c  (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc anti lamin a c
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Anti Lamin A C, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti lamin a c/product/Cell Signaling Technology Inc
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pbabe puro gfp lamin a plasmid  (Addgene inc)
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Addgene inc pbabe puro gfp lamin a plasmid
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Pbabe Puro Gfp Lamin A Plasmid, supplied by Addgene inc, 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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pbabe puro gfp lamin a plasmid - by Bioz Stars, 2026-06
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mouse anti lamin b1 b 10  (Santa Cruz Biotechnology)
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Santa Cruz Biotechnology mouse anti lamin b1 b 10
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Mouse Anti Lamin B1 B 10, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse anti lamin b1 b 10/product/Santa Cruz Biotechnology
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mouse anti lamin b1 b 10 - by Bioz Stars, 2026-06
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anti lamin b1 lmnb1  (Abmart Inc)
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Abmart Inc anti lamin b1 lmnb1
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Anti Lamin B1 Lmnb1, supplied by Abmart Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti lamin b1 lmnb1/product/Abmart Inc
Average 86 stars, based on 1 article reviews
anti lamin b1 lmnb1 - by Bioz Stars, 2026-06
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hot roll laminator  (Cheminstruments Inc)
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Cheminstruments Inc hot roll laminator
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Hot Roll Laminator, supplied by Cheminstruments Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hot roll laminator/product/Cheminstruments Inc
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lamin c  (Developmental Studies Hybridoma Bank)
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Developmental Studies Hybridoma Bank lamin c
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Lamin C, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lamin c/product/Developmental Studies Hybridoma Bank
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lamin c - by Bioz Stars, 2026-06
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mouse anti lamin  (Developmental Studies Hybridoma Bank)
97
Developmental Studies Hybridoma Bank mouse anti lamin
STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained <t>with</t> <t>anti‐Lamin</t> antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.
Mouse Anti Lamin, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse anti lamin/product/Developmental Studies Hybridoma Bank
Average 97 stars, based on 1 article reviews
mouse anti lamin - by Bioz Stars, 2026-06
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Image Search Results


STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained with anti‐Lamin antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.

Journal: Journal of Extracellular Vesicles

Article Title: Systemic Propagation of STING Signalling via Generation of Large Extracellular Vesicles

doi: 10.1002/jev2.70289

Figure Lengend Snippet: STING in Ras V12 , scrib − / − clones plays a key role in controlling the production of large EVs . (a) Images of eye discs with Ras V12 (a’) or Ras V12 , scrib −/− clones (a“‐a”″). Arrowheads indicate the features associated with CIN: a“: chromatin bridge, a”’: micronucleus, and a“”: cytosolic leakage of chromatin. Clonal cells are marked with GFP (green), the nuclear envelope is stained with anti‐Lamin antibody (magenta), and DNA is stained with DAPI (grey). (b) Relative mRNA expression of STING target genes in eye‐antennal discs. Ras V12 discs were prepared at 6 d AEL. Other discs were prepared at 8 d AEL. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (c) Still shots from ex vivo live imaging of eye discs. Arrowheads indicate blebs and EVs. See for full movies. (d) Quantification of EVs generated from eye discs from 8 d AEL larvae. EVs were quantified at 2 h post incubation. N = 3 for each genotype. Mean ± SEMs are shown. *p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one‐way ANOVA. (e) Schematic of experiments used to assess the expression of antimicrobial peptides in the fat body upon manipulation of Sting in eye disc Ras V12 , scrib −/− clones. (f) Relative mRNA expression of antimicrobial peptides in the fat body. Fat body from larvae with Ras V12 eye disc clones was prepared from 6 d AEL larvae. Fat body from other genotypes was prepared from 8 d AEL larvae. Mean ± SEMs are shown. **p < 0.01, *** p < 0.001 one‐way ANOVA.

Article Snippet: Primary antibodies included anti‐pJNK (1:200, Cell Signalling, 4668), anti‐pFak (1:200, Cell Signalling, 700255), and anti‐lamin (1:1000, DSHB, ADL67.10).

Techniques: Clone Assay, Staining, Expressing, Ex Vivo, Imaging, Generated, Incubation