Total lysates (15 µg protein) from Raji (negative control), A549 and mouse brain were resolved by electrophoresis (4-20% Tris-glycine gel), transferred to nitrocellulose, and probed with 1:500 diluted (1 µg/mL) purified anti-Dynamin-1 antibody (upper). Proteins were visualized by chemiluminescence detection using 1:3000 diluted HRP goat anti-mouse-IgG secondary antibody for anti-Dynamin-1 antibody or HRP Donkey anti-rabbit IgG Antibody for GAPDH antibody. 1:2000 dilution of GAPDH (poly6314) antibody was used as a loading control (lower). Lane M: MW ladder.
Total lysates (15 µg protein) from Raji (negative control), A549 and mouse brain were resolved by electrophoresis (4-20% Tris-glycine gel), transferred to nitrocellulose, and probed with 1:500 diluted (1 µg/mL) purified anti-Dynamin-1 antibody (upper). Proteins were visualized by chemiluminescence detection using 1:3000 diluted HRP goat anti-mouse-IgG secondary antibody for anti-Dynamin-1 antibody or HRP Donkey anti-rabbit IgG Antibody for GAPDH antibody. 1:2000 dilution of GAPDH (poly6314) antibody was used as a loading control (lower). Lane M: MW ladder.
Total lysates (15 µg protein) from human brain, mouse brain and rat brain were resolved by electrophoresis (4-12% Bis-Tris gel), transferred to nitrocellulose, and probed with 1:250 diluted (2 µg/mL) purified anti-Dynamin-1 antibody (upper). Proteins were visualized by chemiluminescence detection using 1:3000 diluted HRP goat anti-mouse-IgG secondary antibody. 1:1000 (0.5 micro;g/mL) dilution of β-actin (2F1-1) antibody was used as a loading control (lower). Lane M: MW ladder.
IHC staining of Formalin Fixed Paraffin Embedded (FFPE) normal human brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R, the tissue was incubated with anti-Dynamin-1 antibody (Clone P83G4B6) at 5 µg/mL overnight at 4°C. BioLegend’s Ultra-Streptavidin (USA) HRP kit (Multi-Species, DAB) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. Images were captured with a 40X objective.
IHC staining of Formalin Fixed Paraffin Embedded (FFPE) mouse brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R, the tissue was incubated with anti-Dynamin-1 antibody (Clone P83G4B6) at 5 µg/mL overnight at 4°C. BioLegend’s Ultra-Streptavidin (USA) HRP kit (Multi-Species, DAB) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. Images were captured with a 40X objective.
IHC staining of Formalin Fixed Paraffin Embedded (FFPE) rat brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R, the tissue was incubated with anti-Dynamin-1 antibody (Clone P83G4B6) at 5 µg/mL overnight at 4°C. BioLegend’s Ultra-Streptavidin (USA) HRP kit (Multi-Species, DAB) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. Images were captured with a 40X objective.
Dynamin-1, also known as DMN-1, is a 100 kD protein with GTPase activity. Dynamin-1 is involved in several intracellular trafficking processes including synaptic vesicle recycling, neurotransmitter reuptake and receptor internalization. In addition, Dynamin-1 may be necessary for the establishment and proper maintenance of mature neuronal structure. Studies have shown that Dynamin-1 is upregulated during new neurite formation. Conversely, Dynamin-1 is downregulated during neurite retraction. Silencing the initiation codon for Dynamin limits the formation of axon-like structures.
Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 1:250-1:2500 diluted (0.2 – 2 µg/mL). For immunohistochemical staining on formalin-fixed paraffin-embedded tissue sections, the suggested use of this reagent is 1:100-1:250 diluted (2 – 5 µg/mL). It is recommended that the reagent be titrated for optimal performance for each application.
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