The largest database of trusted experimental protocols

Cu 300 tem grids

Manufactured by Agar Scientific
Sourced in United Kingdom

The Cu-300 TEM grids are copper-based specimen supports designed for use in transmission electron microscopy (TEM) analysis. These grids provide a stable and uniform platform for mounting samples for high-resolution imaging and examination.

Automatically generated - may contain errors

2 protocols using cu 300 tem grids

1

Characterization of Silver Nanoparticles by TEM

Check if the same lab product or an alternative is used in the 5 most similar protocols
For transmission electron microscopy (TEM), the AgNPs were diluted in MQ water, dropped onto the carbon film-covered side of a copper Cu-300 TEM grids (Agar Scientific, Ltd., Essex, UK), air-dried, and imaged with a Tecnai-10 transmission electron microscope (FEI Company, Hillsboro, OR, USA) at 80 kV. The concentration of AgNPs was calculated according to the Beer–Lambert law by measuring the UV–Vis absorbance of AgNPs at 415 nm and using a molar attenuation coefficient of 8.83 × 10−9 M−1 cm−1. For size and zeta potential measurements, the AgNPs were diluted 400X in MQ water. Zetasizer Pro (Malvern Panalytical, Malvern, UK) was used for the measurements. Size measurements were done at 25 °C with the material refractive index (RI) set to 2.00, and material absorption set to 0.200 using polystyrene cuvettes (#DTS0012, Malvern Panalytical, Malvern, UK); zeta potential measurements were done at 25 °C with 12 runs/measurement using capillary cell cuvettes (#DTS1070, Malvern Panalytical, Malvern, UK).
+ Open protocol
+ Expand
2

Negative Staining Transmission Electron Microscopy

Check if the same lab product or an alternative is used in the 5 most similar protocols
Samples were diluted to approx. 1 nM and deposited on glow-discharged formvar-supported carbon-coated Cu300 TEM grids (Agar Scientific). A pseudo-positive staining method was used whereby the grids were incubated with the sample for two minutes, blotted with filter paper, then incubated for 3 seconds on a drop of water. This was followed by a 20-second incubation on a 20 µL drop of 2 % uranyl acetate. After blotting, the sample was placed for 3 seconds on another drop of water followed by filter blotting and air drying. Samples were images in a FEI Tecnai T12 microscope (120 kV) and images recorded on a 16 megapixel Gatan OneView CMOS camera.
+ 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!