The largest database of trusted experimental protocols

Ivis lumina imaging station

Manufactured by PerkinElmer
Sourced in United States

The IVIS Lumina imaging station is a laboratory instrument designed for in vivo and in vitro optical imaging. The system utilizes advanced bioluminescence and fluorescence imaging technologies to enable sensitive detection and quantification of biological processes in small animal models and cell-based assays.

Automatically generated - may contain errors

2 protocols using ivis lumina imaging station

1

Intracranial Tumor Growth Monitoring

Check if the same lab product or an alternative is used in the 5 most similar protocols
BALB/c nude mice were maintained and bred in a specific-pathogen free (SPF) environment, adhering to standard conditions of temperature (20–26 °C) and humidity (40–70%). They were subjected to a strict 12-h light cycle, with lights on at 08:00 a.m. and off at 08:00 p.m. No limitations were imposed on the sex of the experimental animals involved in this study. Cells expressing firefly luciferase mixed with Matrigel (Corning, NY, USA) were intracranially injected into 5- to 6-week-old female athymic nude mice. The intracranial injection point was at the cerebral cortex, 1 mm prior to coronal suture, 1 mm on the right side of the centreline, and 3 mm below the dura mater. Appropriate medications were provided to reduce pain. To monitor intracranial tumour growth, the animals were intraperitoneally injected with D-luciferin (Yeasen, #40902ES01) and anaesthetized with isoflurane. The images were captured using an In Vivo MS FX pro Imaging System (Bruker, MA, USA) or IVIS Lumina imaging station (Perkin Elmer, MA, USA). The results were reported as the total flux (photons/second). The mice were sacrificed at the indicated time points. The brains were removed, fixed in 4% paraformaldehyde, and embedded in paraffin.
+ Open protocol
+ Expand
2

In Vivo Drug Distribution and Pharmacokinetics

Check if the same lab product or an alternative is used in the 5 most similar protocols
Since the drug does not have fluorescence that can be excited, DIR was selected as a fluorescence probe to observe the distribution of the drug in tumor-bearing mice. DIR-loaded PNM and free DIR were injected into tumor-bearing mice (DIR, 1 μg/g per mouse) through the tail vein, and in vivo fluorescence images at 12, 36, 60 and 84 h were obtained by an IVIS Lumina imaging station (PerkinElmer, MA, USA). The main organs (heart, liver, spleen, lung and kidney) and tumors of mice were collected after the mice were euthanized, and measured by an imaging system.
To determine the pharmacokinetic profiles of PNM, 8 weeks old SD rats were divided into two groups: free Flav and PNM (Flav = 2.5 mg/kg, n = 3). After injection of free Flav or PNM, we separately collected 0.5 mL blood samples from the rats at 0.5, 3, 7, 24 and 48 h, and then the blood samples were centrifuged for 10 min at the speed of 3000 rpm to acquire serum. After precipitating the protein with methanol, the concentration of Flav in free Flav group and PNM group were detected by the HPLC-MS/MS (AB SCIEX, MA, 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!