rac1 2 3 Search Results


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rac2 silencing genepharma china  (MedChemExpress)
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anti rac1 2 3  (Cell Signaling Technology Inc)
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rac1  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology rac1
Primer Sequences
Rac1, 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
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anti rac3  (Proteintech)
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Proteintech anti rac3
Primer Sequences
Anti Rac3, supplied by Proteintech, 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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rabbit anti rac1  (ABclonal Biotechnology)
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ABclonal Biotechnology rabbit anti rac1
Primer Sequences
Rabbit Anti Rac1, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rac1/2/3 rabbit mab  (Genecopoeia)
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Genecopoeia rac1/2/3 rabbit mab
Primer Sequences
Rac1/2/3 Rabbit Mab, supplied by Genecopoeia, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rac1-2-3 antibody  (MedChemExpress)
N/A
Rac1-2-3 Antibody (YA6751) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Rac1-2-3.
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anti-rac1-2-3 antibody  (TargetMol)
N/A
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rac1/2/3 fusion protein  (Proteintech)
N/A
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rac1/2/3 rabbit mab  (ABclonal)
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Image Search Results


Primer Sequences

Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

Article Title: Exosomal Micro‐RNA‐96 Derived From Bone Marrow Mesenchymal Stem Cells Inhibits Doxorubicin‐Induced Myocardial Toxicity by Inhibiting the Rac1/Nuclear Factor‐κB Signaling Pathway

doi: 10.1161/JAHA.120.020589

Figure Lengend Snippet: Primer Sequences

Article Snippet: After being confined in bovine serum albumin, the proteins were incubated with primary antibodies of Rac1 (sc‐514583, 1:1000), phosphorylated (p)‐IKKα (sc‐166231, 1:1000), IKKα (sc‐166231, 1:1000), p‐IKKβ (sc‐23470‐R, 1:1000), IKKβ (sc‐8014, 1:1000), p65 (sc‐8008, 1:200) (Santa Cruz Biotechnology), p‐IκBα (#4814, 1:1000), IκBα (#9246, 1:1000) and p‐p65 (#3033, 1:1000) (Cell Signaling Technology).

Techniques:

A and B , The expression of Rac1 in the myocardium measured by quantitative real time polymerase chain reaction and Western blotting. C , the levels of p‐IKKα, p‐IKKβ, p‐IκBα, and p‐p65 measured by Western blotting; 8 rats for each group. Exo+inhibitor indicates exosome plus inhibitor; Exo+mimic, exosome plus mimic; Exo+miR‐96, exosome plus microRNA‐96; and negative control (NC). * P <0.05, compared with the normal group; ‡ P <0.05, compared with the doxorubicin group; † P <0.05, compared with the exosome+mimic NC group; and § P <0.05, compared with the exosome+inhibitor NC group; data were presented as mean±SD; data were analyzed using 1‐way ANOVA and the Tukey test was applied for post hoc multiple comparisons.

Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

Article Title: Exosomal Micro‐RNA‐96 Derived From Bone Marrow Mesenchymal Stem Cells Inhibits Doxorubicin‐Induced Myocardial Toxicity by Inhibiting the Rac1/Nuclear Factor‐κB Signaling Pathway

doi: 10.1161/JAHA.120.020589

Figure Lengend Snippet: A and B , The expression of Rac1 in the myocardium measured by quantitative real time polymerase chain reaction and Western blotting. C , the levels of p‐IKKα, p‐IKKβ, p‐IκBα, and p‐p65 measured by Western blotting; 8 rats for each group. Exo+inhibitor indicates exosome plus inhibitor; Exo+mimic, exosome plus mimic; Exo+miR‐96, exosome plus microRNA‐96; and negative control (NC). * P <0.05, compared with the normal group; ‡ P <0.05, compared with the doxorubicin group; † P <0.05, compared with the exosome+mimic NC group; and § P <0.05, compared with the exosome+inhibitor NC group; data were presented as mean±SD; data were analyzed using 1‐way ANOVA and the Tukey test was applied for post hoc multiple comparisons.

Article Snippet: After being confined in bovine serum albumin, the proteins were incubated with primary antibodies of Rac1 (sc‐514583, 1:1000), phosphorylated (p)‐IKKα (sc‐166231, 1:1000), IKKα (sc‐166231, 1:1000), p‐IKKβ (sc‐23470‐R, 1:1000), IKKβ (sc‐8014, 1:1000), p65 (sc‐8008, 1:200) (Santa Cruz Biotechnology), p‐IκBα (#4814, 1:1000), IκBα (#9246, 1:1000) and p‐p65 (#3033, 1:1000) (Cell Signaling Technology).

Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot, Negative Control

A , The expressions of micorRNA‐96 and Rac1 in H9c2 cells. B , The protein level of Rac1. C , The levels of p‐IKKα, p‐IKKβ, p‐IκBα, and p‐65 in H9c2 cells; n=3. Exo+inhibitor indicates exosome plus inhibitor; Exo+mimic, exosome plus mimic; Exo+miR‐96, exosome plus microRNA‐96; and NC, negative control. * P <0.05, compared with the control group; ‡ P <0.05, compared with the doxorubicin group; † P <0.05, compared with the exosome+mimic NC group; and § P <0.05, compared with the exosome+inhibitor NC group; $ P <0.05, compared with the exosome+miR‐96 inhibitor+NC siRNA group; data were presented as mean±SD; data were analyzed using 1‐way ANOVA and the Tukey test was applied for post hoc multiple comparisons.

Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

Article Title: Exosomal Micro‐RNA‐96 Derived From Bone Marrow Mesenchymal Stem Cells Inhibits Doxorubicin‐Induced Myocardial Toxicity by Inhibiting the Rac1/Nuclear Factor‐κB Signaling Pathway

doi: 10.1161/JAHA.120.020589

Figure Lengend Snippet: A , The expressions of micorRNA‐96 and Rac1 in H9c2 cells. B , The protein level of Rac1. C , The levels of p‐IKKα, p‐IKKβ, p‐IκBα, and p‐65 in H9c2 cells; n=3. Exo+inhibitor indicates exosome plus inhibitor; Exo+mimic, exosome plus mimic; Exo+miR‐96, exosome plus microRNA‐96; and NC, negative control. * P <0.05, compared with the control group; ‡ P <0.05, compared with the doxorubicin group; † P <0.05, compared with the exosome+mimic NC group; and § P <0.05, compared with the exosome+inhibitor NC group; $ P <0.05, compared with the exosome+miR‐96 inhibitor+NC siRNA group; data were presented as mean±SD; data were analyzed using 1‐way ANOVA and the Tukey test was applied for post hoc multiple comparisons.

Article Snippet: After being confined in bovine serum albumin, the proteins were incubated with primary antibodies of Rac1 (sc‐514583, 1:1000), phosphorylated (p)‐IKKα (sc‐166231, 1:1000), IKKα (sc‐166231, 1:1000), p‐IKKβ (sc‐23470‐R, 1:1000), IKKβ (sc‐8014, 1:1000), p65 (sc‐8008, 1:200) (Santa Cruz Biotechnology), p‐IκBα (#4814, 1:1000), IκBα (#9246, 1:1000) and p‐p65 (#3033, 1:1000) (Cell Signaling Technology).

Techniques: Negative Control, Control

A , TargetScan predicted the sequences of the binding sites between microRNA‐96 and Rac1. B , Dual‐luciferase reporter assay verified the targeting relationship between microRNA‐96 and Rac1 (n=3); data were presented as mean±SD and analyzed by the student t ‐test. miR‐96 indicates microRNA‐96; MUT, mutated‐type; NC, negative control; and WT, wild‐type.

Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

Article Title: Exosomal Micro‐RNA‐96 Derived From Bone Marrow Mesenchymal Stem Cells Inhibits Doxorubicin‐Induced Myocardial Toxicity by Inhibiting the Rac1/Nuclear Factor‐κB Signaling Pathway

doi: 10.1161/JAHA.120.020589

Figure Lengend Snippet: A , TargetScan predicted the sequences of the binding sites between microRNA‐96 and Rac1. B , Dual‐luciferase reporter assay verified the targeting relationship between microRNA‐96 and Rac1 (n=3); data were presented as mean±SD and analyzed by the student t ‐test. miR‐96 indicates microRNA‐96; MUT, mutated‐type; NC, negative control; and WT, wild‐type.

Article Snippet: After being confined in bovine serum albumin, the proteins were incubated with primary antibodies of Rac1 (sc‐514583, 1:1000), phosphorylated (p)‐IKKα (sc‐166231, 1:1000), IKKα (sc‐166231, 1:1000), p‐IKKβ (sc‐23470‐R, 1:1000), IKKβ (sc‐8014, 1:1000), p65 (sc‐8008, 1:200) (Santa Cruz Biotechnology), p‐IκBα (#4814, 1:1000), IκBα (#9246, 1:1000) and p‐p65 (#3033, 1:1000) (Cell Signaling Technology).

Techniques: Binding Assay, Luciferase, Reporter Assay, Negative Control