rabbit anti mouse bfgf monoclonal antibody Search Results


93
Sino Biological rabbit anti mouse antibody
Rabbit Anti Mouse Antibody, supplied by Sino Biological, 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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Cell Signaling Technology Inc anti mouse
Anti Mouse, supplied by Cell Signaling Technology Inc, 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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96
Jackson Immuno peroxidase conjugated igg fraction monoclonal mouse anti rabbit
Peroxidase Conjugated Igg Fraction Monoclonal Mouse Anti Rabbit, supplied by Jackson Immuno, 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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Cell Signaling Technology Inc rabbit anti mouse total mlc ab
Rabbit Anti Mouse Total Mlc Ab, supplied by Cell Signaling Technology Inc, 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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93
Jackson Immuno anti rabbit secondary
Anti Rabbit Secondary, supplied by Jackson Immuno, 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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Cell Signaling Technology Inc anti mouse igg hrp
Anti Mouse Igg Hrp, supplied by Cell Signaling Technology Inc, 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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Cell Signaling Technology Inc anti rabbit
Anti Rabbit, supplied by Cell Signaling Technology Inc, 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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92
Jackson Immuno anti rabbit igg
Anti Rabbit Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno anti rabbit immunoglobulin g igg conjugated alkaline phosphatases
Anti Rabbit Immunoglobulin G Igg Conjugated Alkaline Phosphatases, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno mouse anti rabbit light chain
Mouse Anti Rabbit Light Chain, supplied by Jackson Immuno, 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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Jackson Immuno dylight 549 conjugated mouse anti rabbit
Fig. 2. Localization and expression of myogenic regulatory transcription factors (MRFs) during proliferation and differentiation. (A) Proliferating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and rabbit anti-MyoD, followed by <t>DyLight</t> <t>649-conjugated</t> donkey anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (B) Cells differentiated for 3 days were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and goat anti-Myogenin, followed by DyLight 649-conjugated donkey anti-goat (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Arrows indicate Myogenin positive cells. Scale bar 10 mM. (C) Differentiating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green) and rabbit anti-Desmin, followed by DyLight <t>549-conjugated</t> mouse anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (D) Left: a representative western blot showing the expression level of MyoD and Desmin after 0 and 3 days of differentiation. Cell lysates were subjected to western blotting using antibodies to MyoD, Desmin, and Tubulin (loading control). Right: quantification of Western blots. Bars show the expression of Desmin and MyoD, relative to tubulin, after 0 and 3 days of differentiation. The graph represents the average of three experiments with SD.
Dylight 549 Conjugated Mouse Anti Rabbit, supplied by Jackson Immuno, 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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93
Jackson Immuno light chain specific irdye 800w secondary antibody
Fig. 2. Localization and expression of myogenic regulatory transcription factors (MRFs) during proliferation and differentiation. (A) Proliferating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and rabbit anti-MyoD, followed by <t>DyLight</t> <t>649-conjugated</t> donkey anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (B) Cells differentiated for 3 days were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and goat anti-Myogenin, followed by DyLight 649-conjugated donkey anti-goat (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Arrows indicate Myogenin positive cells. Scale bar 10 mM. (C) Differentiating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green) and rabbit anti-Desmin, followed by DyLight <t>549-conjugated</t> mouse anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (D) Left: a representative western blot showing the expression level of MyoD and Desmin after 0 and 3 days of differentiation. Cell lysates were subjected to western blotting using antibodies to MyoD, Desmin, and Tubulin (loading control). Right: quantification of Western blots. Bars show the expression of Desmin and MyoD, relative to tubulin, after 0 and 3 days of differentiation. The graph represents the average of three experiments with SD.
Light Chain Specific Irdye 800w Secondary Antibody, supplied by Jackson Immuno, 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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Average 93 stars, based on 1 article reviews
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Image Search Results


Fig. 2. Localization and expression of myogenic regulatory transcription factors (MRFs) during proliferation and differentiation. (A) Proliferating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and rabbit anti-MyoD, followed by DyLight 649-conjugated donkey anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (B) Cells differentiated for 3 days were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and goat anti-Myogenin, followed by DyLight 649-conjugated donkey anti-goat (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Arrows indicate Myogenin positive cells. Scale bar 10 mM. (C) Differentiating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green) and rabbit anti-Desmin, followed by DyLight 549-conjugated mouse anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (D) Left: a representative western blot showing the expression level of MyoD and Desmin after 0 and 3 days of differentiation. Cell lysates were subjected to western blotting using antibodies to MyoD, Desmin, and Tubulin (loading control). Right: quantification of Western blots. Bars show the expression of Desmin and MyoD, relative to tubulin, after 0 and 3 days of differentiation. The graph represents the average of three experiments with SD.

Journal: Differentiation; research in biological diversity

Article Title: The combination of glycosaminoglycans and fibrous proteins improves cell proliferation and early differentiation of bovine primary skeletal muscle cells.

doi: 10.1016/j.diff.2013.06.006

Figure Lengend Snippet: Fig. 2. Localization and expression of myogenic regulatory transcription factors (MRFs) during proliferation and differentiation. (A) Proliferating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and rabbit anti-MyoD, followed by DyLight 649-conjugated donkey anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (B) Cells differentiated for 3 days were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green), and goat anti-Myogenin, followed by DyLight 649-conjugated donkey anti-goat (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Arrows indicate Myogenin positive cells. Scale bar 10 mM. (C) Differentiating cells were fixed with 2% PFA, immunostained with Alexa 488-Phalloidin (green) and rabbit anti-Desmin, followed by DyLight 549-conjugated mouse anti-rabbit (red) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 10 mM. (D) Left: a representative western blot showing the expression level of MyoD and Desmin after 0 and 3 days of differentiation. Cell lysates were subjected to western blotting using antibodies to MyoD, Desmin, and Tubulin (loading control). Right: quantification of Western blots. Bars show the expression of Desmin and MyoD, relative to tubulin, after 0 and 3 days of differentiation. The graph represents the average of three experiments with SD.

Article Snippet: Alexa 488-conjugated goat anti-mouse and DyLight 549- conjugated mouse anti-rabbit were from Jackson ImmunoResearch Laboratories Inc. (West Grove, PA, USA).

Techniques: Expressing, Microscopy, Staining, Western Blot, Control

Fig. 6. Desmin staining of myotubes on different surface coatings after 1, 3 or 5 days in differentiation medium. Differentiating cells were fixed with 2% PFA and immunostained with rabbit anti-Desmin, followed by DyLight 549-conjugated mouse anti-rabbit (yellow) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 20 mM.

Journal: Differentiation; research in biological diversity

Article Title: The combination of glycosaminoglycans and fibrous proteins improves cell proliferation and early differentiation of bovine primary skeletal muscle cells.

doi: 10.1016/j.diff.2013.06.006

Figure Lengend Snippet: Fig. 6. Desmin staining of myotubes on different surface coatings after 1, 3 or 5 days in differentiation medium. Differentiating cells were fixed with 2% PFA and immunostained with rabbit anti-Desmin, followed by DyLight 549-conjugated mouse anti-rabbit (yellow) before fluorescence microscopy analysis. Nuclei were stained with DAPI (blue). Scale bar 20 mM.

Article Snippet: Alexa 488-conjugated goat anti-mouse and DyLight 549- conjugated mouse anti-rabbit were from Jackson ImmunoResearch Laboratories Inc. (West Grove, PA, USA).

Techniques: Staining, Microscopy