The largest database of trusted experimental protocols

Jsm 5200 electron probe microanalyzer

Manufactured by JEOL
Sourced in Japan

The JSM 5200 is an electron probe microanalyzer manufactured by JEOL. It is designed to perform elemental analysis and mapping of solid samples. The instrument uses a focused electron beam to interact with the sample, and the emitted X-rays are detected and analyzed to determine the chemical composition of the material.

Automatically generated - may contain errors

Lab products found in correlation

2 protocols using jsm 5200 electron probe microanalyzer

1

Preparing Infected Skin Samples for SEM

Check if the same lab product or an alternative is used in the 5 most similar protocols
The samples fixed in 10 % buffered formalin were prepared according to Bullard et al. (2012) (link), with minor changes. Briefly, different parts of the infected skin were washed several times using phosphate buffer saline (pH 7.2), then fixed in 2.5 % glutaraldehyde at 4°C for 24 hours. The samples were dehydrated by passing them through serial ascending concentrations of ethanol (50 % to 100 %; each for a duration of 20 minutes). The specimens were then dehydrated on filter paper (Whatman Grade 1, Cat. No. 1001110); complete dryness occurred in a CO2 critical point drier (Autosamdri-815, Germany). The samples were then glued onto stubs, coated with 20nm gold in a sputter coater (Spi-Module Sputter Coater, UK), examined and photographed using a JSM 5200 electron probe microanalyzer (JEOL, Japan) at the College of Agriculture, Cairo University, Egypt.
+ Open protocol
+ Expand
2

Morphological Analysis of L. cyprinacea Copepods

Check if the same lab product or an alternative is used in the 5 most similar protocols
Five parasite females of L. cyprinacea subjected to Illicium verum were harvested and rinsed multiple times with saline. The copepods were rinsed multiple times with saline, then cleaned in lactophenol and loaded on gelatin to analyze their morphology [21 (link),42 (link)]. Five freshly obtained copepods were rinsed multiple times in saline. Adult L. cyprinacea was immersed in 2.5% glutaraldehyde. After that, the specimens were dehydrated in an increasing ethanol series, dried in a CO2 critical point drier (Autosamdri-815; Lewis Avenue, Rockville, ML, USA), bonded over stubs, and sputter-covered with twenty nm gold (Spi-Module sputter coater; UK). Then, the specimens were inspected and photographed using a scanning electron microscope (SEM) at magnifications ranging from 35 to 500 (JEOL JSM 5200 Electron Probe Microanalyzer; Tokyo, Japan) [21 (link)].
+ 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!