mouse anti cor Search Results


99
LI-COR ir dye
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Thermo Fisher mouse taqman probe invitrogen mm04277571 licor irdye 800cw goat anti rat igg li cor biosciences
Mouse Taqman Probe Invitrogen Mm04277571 Licor Irdye 800cw Goat Anti Rat Igg Li Cor Biosciences, supplied by Thermo Fisher, 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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LI-COR mouse α actin
Mouse α Actin, supplied by LI-COR, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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LI-COR irdye 680ltconjugated donkey anti mouse igg h l
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LI-COR fluorophore conjugated antibodies for nir
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LI-COR irdye 800cw goat antimouse
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96
LI-COR β actin
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
β Actin, supplied by LI-COR, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
LI-COR irdye680rd
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
Irdye680rd, supplied by LI-COR, 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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LI-COR fluorescent donkey anti mouse irdye 800cw
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
Fluorescent Donkey Anti Mouse Irdye 800cw, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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LI-COR irdye 800cw goat anti mouse igg
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
Irdye 800cw Goat Anti Mouse Igg, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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LI-COR irdye680 conjugated goat anti mouse
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
Irdye680 Conjugated Goat Anti Mouse, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
LI-COR goat anti mouse antibody
A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and <t>β-actin</t> of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.
Goat Anti Mouse Antibody, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and β-actin of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.

Journal: PLoS ONE

Article Title: Effect of progesterone on Smad signaling and TGF-β/Smad-regulated genes in lung epithelial cells

doi: 10.1371/journal.pone.0200661

Figure Lengend Snippet: A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). qPCR of CTGF mRNA was performed after 12 h ( A ) and western blotting analysis after 24 h ( B ). Relative mRNA levels of CTGF were calculated by normalizing signals to detected GAPDH mRNA. Differences compared with untreated cells were calculated. Means + SD of at least n = 3 independent experiments are shown. In B , a representative immunoblot of CTGF and β-actin of n = 3 independent experiments is shown. ** p < 0.01 compared with control cells; ## p < 0.01 compared with cells treated with TGF-β1.

Article Snippet: Membranes were blocked in 5% bovine serum albumin and incubated with primary antibodies recognizing CTGF (ab6992; Abcam, Cambridge, UK), transgelin (sc-50446; Santa Cruz Biotechnology, Santa Cruz, CA), anti-Smad2/3-P (kind gift from Dr. C.-H. Heldin, Ludwig Institute for Cancer Research, Uppsala, Sweden), and β-actin (926–42212; LI-COR Inc., Lincoln, NE, USA), followed by staining with an horseradish peroxidase conjugated goat anti rabbit IgG (Thermo Fisher Scientific).

Techniques: Incubation, Western Blot

A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). Promoter analysis ( A ) and qPCR of transgelin ( TAGLN ) mRNA ( B ) were performed after 12 h, and western blotting analysis ( C ) after 72 h. Relative mRNA levels of TAGLN were calculated by normalizing signals to detected GAPDH mRNA ( B ) and compared with untreated cells. Means + SD of at least n = 3 independent experiments are shown. In C , a representative immunoblot of transgelin and β-actin of n = 3 independent experiments is shown. ** p < 0.01 and *** p < 0.001 compared with control cells; # p < 0.05, ## p < 0.01, and ### p < 0.001 compared with cells treated with TGF-β1.

Journal: PLoS ONE

Article Title: Effect of progesterone on Smad signaling and TGF-β/Smad-regulated genes in lung epithelial cells

doi: 10.1371/journal.pone.0200661

Figure Lengend Snippet: A549 cells were incubated with TGF-β1 (10 ng/mL) and progesterone (10 μg/mL). Promoter analysis ( A ) and qPCR of transgelin ( TAGLN ) mRNA ( B ) were performed after 12 h, and western blotting analysis ( C ) after 72 h. Relative mRNA levels of TAGLN were calculated by normalizing signals to detected GAPDH mRNA ( B ) and compared with untreated cells. Means + SD of at least n = 3 independent experiments are shown. In C , a representative immunoblot of transgelin and β-actin of n = 3 independent experiments is shown. ** p < 0.01 and *** p < 0.001 compared with control cells; # p < 0.05, ## p < 0.01, and ### p < 0.001 compared with cells treated with TGF-β1.

Article Snippet: Membranes were blocked in 5% bovine serum albumin and incubated with primary antibodies recognizing CTGF (ab6992; Abcam, Cambridge, UK), transgelin (sc-50446; Santa Cruz Biotechnology, Santa Cruz, CA), anti-Smad2/3-P (kind gift from Dr. C.-H. Heldin, Ludwig Institute for Cancer Research, Uppsala, Sweden), and β-actin (926–42212; LI-COR Inc., Lincoln, NE, USA), followed by staining with an horseradish peroxidase conjugated goat anti rabbit IgG (Thermo Fisher Scientific).

Techniques: Incubation, Western Blot