anti human fgf2 antibody (Cell Signaling Technology Inc)
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Anti Human Fgf2 Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+fgf2+antibody/Basic+FGF+Antibody/pmc12874654-109-32-35
Average 94 stars, based on 45 article reviews
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Membrane:Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Western blot analysis Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% mercaptoethanol (1:3 v/v) and boiled at 97 C for 5 min. Each Sample (40 l) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (antihuman FGF1 antibody (Cell Signaling Technology #3139) or Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% β-mercaptoethanol (1:3 v/v) and boiled at 97 °C for 5 min. Each Sample (40 μl) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (anti-human FGF1 antibody (Cell Signaling Technology #3139) or Saline:Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Western blot analysis Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% mercaptoethanol (1:3 v/v) and boiled at 97 C for 5 min. Each Sample (40 l) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (antihuman FGF1 antibody (Cell Signaling Technology #3139) or Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% β-mercaptoethanol (1:3 v/v) and boiled at 97 °C for 5 min. Each Sample (40 μl) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (anti-human FGF1 antibody (Cell Signaling Technology #3139) or Incubation:Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Western blot analysis Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% mercaptoethanol (1:3 v/v) and boiled at 97 C for 5 min. Each Sample (40 l) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (antihuman FGF1 antibody (Cell Signaling Technology #3139) or Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% β-mercaptoethanol (1:3 v/v) and boiled at 97 °C for 5 min. Each Sample (40 μl) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (anti-human FGF1 antibody (Cell Signaling Technology #3139) or Cell-Signaling:Article Title: Implantation of human mesenchymal stromal cell (MSC)-pellet for therapeutic angiogenesis Article Snippet: Mouse plasma was mixed with X4 Laemmli buffer containing 2.5% β-mercaptoethanol (1:3 v/v) and boiled at 97 °C for 5 min. Each Sample (40 μl) was loaded on SDS-PAGE gel (Bio-Rad) and transferred to nitrocellulose membrane (Bio-Rad). .. Membrane was blocked with 5% dry milk in phosphate-buffered saline-Tween (PBST) at room temperature (RT) for 1 hour and subsequently incubated with primary antibody (anti-human FGF1 antibody (Cell Signaling Technology #3139) or |

