The largest database of trusted experimental protocols

Spark fluorometric plate reader

Manufactured by Tecan

The Spark fluorometric plate reader is a versatile laboratory instrument used for the detection and quantification of fluorescent signals in microplate-based assays. It provides reliable and accurate measurements of fluorescence intensity, making it a valuable tool for a wide range of applications in life science research, drug discovery, and clinical diagnostics.

Automatically generated - may contain errors

2 protocols using spark fluorometric plate reader

1

Quantification of Cellular Cholesterol Levels

Check if the same lab product or an alternative is used in the 5 most similar protocols
An Amplex Red cholesterol fluorometric detection assay (Thermo-Fischer, A12216) was used for quantification of total cholesterol levels in cell culture. Cells were cultured as for immunostaining, treated as indicated in experimental set-up for a total of 72 h. For collection of samples, cell media was removed, and cells rinsed with PBS. Lipids were extracted with a solution of chloroform:methanol (at a ratio of 1:2) for 30+ minutes at 4 °C. Extraction buffer was collected and centrifuged at 10,000 rpm for 10 min at 4 °C to pellet any remaining cell debris; supernatants were collected and stored at −80 °C until assay could be performed. Amplex Red assay was carried out according to manufacturer instructions, with samples diluted 1:1 (a total of 25 μL from each well used per reaction) with 1X reaction buffer. Assay reaction was carried out on a 96 well plate, which was read using a Tecan Spark fluorometric plate reader for quantification.
+ Open protocol
+ Expand
2

Quantification of Cellular Cholesterol Levels

Check if the same lab product or an alternative is used in the 5 most similar protocols
An Amplex Red cholesterol fluorometric detection assay (Thermo-Fischer, A12216) was used for quantification of total cholesterol levels in cell culture. Cells were cultured as for immunostaining, treated as indicated in experimental set-up for a total of 72 h. For collection of samples, cell media was removed, and cells rinsed with PBS. Lipids were extracted with a solution of chloroform:methanol (at a ratio of 1:2) for 30+ minutes at 4 °C. Extraction buffer was collected and centrifuged at 10,000 rpm for 10 min at 4 °C to pellet any remaining cell debris; supernatants were collected and stored at −80 °C until assay could be performed. Amplex Red assay was carried out according to manufacturer instructions, with samples diluted 1:1 (a total of 25 μL from each well used per reaction) with 1X reaction buffer. Assay reaction was carried out on a 96 well plate, which was read using a Tecan Spark fluorometric plate reader for quantification.
+ 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!