The largest database of trusted experimental protocols

2 protocols using anti dynamin 2

1

Analyzing Alzheimer's Disease Pathways

Check if the same lab product or an alternative is used in the 5 most similar protocols
All chemicals and reagents were purchased from Sigma–Aldrich (Poole, UK), Fisher Scientific (Leicester, UK) or Vector Laboratories Ltd (Peterborough, UK) unless specified. Antibodies used were: anti N-APP (22C11; WB 1:500, IHC 1:20) and total and phospho anti-GSK-3α/β (1:750) (Millipore, Watford, UK); anti-Aβ (6E10, BioLegend, San Diego, CA, USA); anti-clathrin heavy chain (CHC) (Clone 23; WB 1:1200, IHC 1;20), anti-caveolin-2 (Clone 65; WB 1:200, IHC 1:50), anti-flotillin-1 (Clone 18; 1:300) and anti-dynamin-2 (1:500) (BD Biosciences, Oxford, UK); anti-BACE1 (1:500, Merck Chemicals Ltd. Nottingham, UK); anti-AP180 (LP2D11; 1:750), anti-PICALM (WB 1:700, IHC 1:100), anti-flotillin-2 (1:500) and anti-AP-2 (1:500) (Novus Biologicals, Littleton, CO, USA); anti-caveolin-1 (WB 1:800, IHC 1:100, Cell Signalling Technology, Beverly, MA, USA); anti-caveolin-3 (1:200), anti-presenilin-1 (PS-1, 1:250), anti-ADAM10 (1:5000), anti-SORLA (EPR14670; 1:400), anti-dynamin-1 (1:300) and anti-BIN-1 (1:100) (Abcam, Cambridge, MA); anti-Rab5 (S-19; WB 1:300, IHC 1:30, Santa Cruz Biotechnology, Santa Cruz, CA, USA) and total tau (1:2000, Dako, Hamburg, Germany). Monoclonal anti-phospho-tau Ser396/Ser404 (PHF-1, 1:100) was a generous gift from Prof. Peter Davies, Albert Einstein College of Medicine, Bronx, NY, USA.
+ Open protocol
+ Expand
2

Protein Expression Analysis of Cells Treated with SBHA and MS-275

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cells were treated with SBHA (20 μM) or MS-275 (2 μM) for 24 h. Cells were lysed in NP-40 (Elpisbio, Daejeon, Korea) in the presence of a protease inhibitor cocktail (Sigma-Aldrich). Protein concentration was determined using the bicinchoninic acid protein assay (Pierce Rockford, IL Waltham, MA, USA). Each sample was separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and electroblotted onto a polyvinyl difluoride (PVDF) membrane. Membranes were incubated with anti-dynamin-2 (BD Bioscience), anti-clathrin (Abcam, Cambridge, UK), and anti-β-actin (Santa Cruz) Abs then incubated with either horseradish peroxidase (HRP)-conjugated anti-rabbit IgG (Cell signaling technology, Beverly, MA, USA) or HRP-conjugated anti-mouse IgG (Cell signaling technology) secondary Abs. Blots were visualized using a super-signal chemiluminescence kit (Pierce, Rockford, IL, USA) and developed using image quant LAS 4000 (GE Lifesciences, Pittsburgh, PA, USA).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!