The largest database of trusted experimental protocols

Formvar film

Manufactured by ProSciTech
Sourced in Australia

Formvar film is a type of thin, transparent film used for various applications in scientific research and laboratory settings. It is primarily composed of polyvinyl formal and serves as a supporting material for specimens in electron microscopy. Formvar film provides a stable and reliable substrate for the preparation and examination of samples under electron microscopic analysis.

Automatically generated - may contain errors

7 protocols using formvar film

1

Transmission Electron Microscopy of AuNP-Treated HMVECs

Check if the same lab product or an alternative is used in the 5 most similar protocols
HMVECs were treated by AuNPs of three different sizes for 30 min and then washed twice by PBS. The cells were fixed by the mixture of 2.5% glutaraldehyde and 0.1 m sodium cacodylate overnight at 4°C, followed by osmium tetroxide polymerization (2%, 30 min at 20°C), uranyl acetate staining (1% overnight), and resin embedding (24 h, 60°C). Thick slices of 70 nm were prepared using a histo diamond knife (DiATOME, Switzerland) and a Leica EM UC6 microtome. The slices were placed on carbon‐coated copper grids (100 mesh, formvar film, ProSciTech), and images captured using a HITACHI HT7700 transmission electron microscopy operated at 80 kV.
+ Open protocol
+ Expand
2

Characterizing Nanoparticles via STEM

Check if the same lab product or an alternative is used in the 5 most similar protocols
Scanning transmission electron microscopy (STEM) was performed using a Carl Zeiss Ultra Plus Field Emission Gun SEM. Copper 100 mesh STEM grids with formvar film (Proscitech, Australia) were dipped into a small drop of each GNP solution. The grid was quickly retracted and allowed to dry. The images were taken at an acceleration voltage of 30 kV using a STEM detector.
+ Open protocol
+ Expand
3

Transmission Electron Microscopy of Amyloid-Beta

Check if the same lab product or an alternative is used in the 5 most similar protocols
For TEM imaging, 5 μL of AβO and Aβf (each of 50 μM), plasma proteins, Aβo, and Aβf in interaction with plasma proteins were pipetted onto copper grids (400 mesh, glow-discharged for 15 s; Formvar film, ProSciTech) and let to adsorb for 1 min. After removing unbound samples by filter paper the grids were rinsed with 10 μL of Milli-Q water. The grids were then negatively stained with 5 μL of 1% uranyl acetate (UA) for 30 s and blown dry. The samples were imaged by a transmission electron microscope (Tecnai G2 F20, FEI, Eindhoven, The Netherlands) under an electric potential of 200 kV. Images were acquired with a CCD camera (UltraScan 1000, Gatan).
+ Open protocol
+ Expand
4

TEM Imaging and EDX Analysis of IAPP and GQDs

Check if the same lab product or an alternative is used in the 5 most similar protocols
High-resolution TEM imaging and energy-dispersive X-ray spectroscopy (EDX) elemental analysis were performed on a Tecnai G2 F20 Transmission Electron Microscope (FEI, Eindhoven, The Netherlands) operated at 200 kV. Briefly, 400 mesh copper grids (Formvar film, ProSciTech) were glow discharged and IAPP (25 μM), GQDs (500 μg/mL) or GQDs pre-incubated with IAPP, which were dissolved/suspended in Milli-Q water for 24 h, were placed onto the grids. Negative staining by 1 % uranyl acetate was performed before imaging. Images were recorded using an UltraScan 1000 P 2k CCD camera (Gatan, California, USA) and Gatand Digital Micrograph 3.9.5 software.
+ Open protocol
+ Expand
5

Characterization of Gold Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
For TEM imaging of the AuNPs, 5 µL of the samples were pipetted on carbon‐coated copper grids (400 mesh, formvar film, ProSciTech). After 60 s of absorption, an excess sample was drawn off using filter paper and grids were washed once with 10 µL of Milli‐Q water. The samples were imaged on a HITACHI HT7700 transmission electron microscopy operated at 80 kV. ImageJ (FIJI) software was used to analyze the images. The absorbance of the AuNPs was obtained by spectra scanning from wavelength of 400 to 800 nm with a UV‐VIS spectrophotometer (UV‐3600, Shimadzu). The hydrodynamic diameter and ζpotential of the AuNPs were determined by dynamic light scattering (DLS) analysis with a Zetasizer (Malvern).
+ Open protocol
+ Expand
6

Transmission Electron Microscopy of Fibrils

Check if the same lab product or an alternative is used in the 5 most similar protocols
Carbon-coated copper grids (400 mesh, formvar film, ProSciTech) were glow-discharged for 15 s prior to deposition of samples (5 μL). After 70 s of absorption, excess sample was drawn off using filter paper and grids washed 1× with 10 μL MilliQ water. For negative staining, grids were exposed to 5 μL of 1% uranyl acetate (UA) for 30 s, with excess stain drawn off as previously and grids allowed to air-dry. The samples were imaged on a Tecnai G2 F20 transmission electron microscope (FEI, 200 kV) with UltraScan 1000 P 2k CCD camera (Gatan) and Gatan Digital Micrograph 3.9.5 software utilized for the acquisition and processing of images. ImageJ (FIJI) was used to extract features such as fibril length and thickness.
+ Open protocol
+ Expand
7

Imaging IAPP Aggregates with L/R-SiO2

Check if the same lab product or an alternative is used in the 5 most similar protocols
For this measurement, 5 μL of the L/R-SiO2 (0.2 mg/mL) was allowed to interact with IAPP monomers (5 μL of 50 μM; freshly dissolved in water, termed as ‘0 h IAPP’ from here onwards), oligomers/protofibrils (1 h into fibrillization, termed as ‘1 h IAPP’), and fibrils (48 h into fibrillization, termed as ‘48 h IAPP’) for 24 h of incubation. The samples were then pipetted onto 15 s glow-discharged 400 mesh copper grids (Formvar film, ProSciTech) for 60 s of adsorption. Excess samples were drawn off by filter paper and the grids were washed using 10 μL of Milli-Q water, with excess drawn off. The grids were then negatively stained with 5 μL of 1% uranyl acetate (UA) for 30 s with excess stain drawn off and air-dried. Samples were characterized on a Tecnai G2 F20 transmission electron microscope (FEI, Eindhoven, The Netherlands) operated at a voltage of 200 kV. Images were recorded using an UltraScan 1000 P 2k CCD camera (Gatan, California, USA) and Gatan Digital Micrograph 3.9.5 software.
+ 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!