Abstract
Peritoneal macrophages (PMs) have been shown to have higher stability compared to other macrophage subtypes. However, obtaining enough PMs from a single mouse is often a limitation for metabolomics analysis. Here, we describe a protocol to isolate metabolites from a small number of mouse primary PMs for 13C-stable glucose tracing and metabolomics. Our protocol uses X for metabolite extraction instead of methanol. Our protocol can consistently extract metabolites from low cell number samples with fewer steps than methanol-based approaches. For complete details on the use and execution of this protocol, please refer to De Jesus et al., (2022).
| Original language | English (US) |
|---|---|
| Article number | 101668 |
| Journal | STAR Protocols |
| Volume | 3 |
| Issue number | 4 |
| DOIs | |
| State | Published - Dec 16 2022 |
| Externally published | Yes |
Keywords
- Cell isolation
- Immunology
- Mass spectrometry
- Metabolism
- Metabolomics
ASJC Scopus subject areas
- General Neuroscience
- General Biochemistry, Genetics and Molecular Biology
- General Immunology and Microbiology
Fingerprint
Dive into the research topics of 'Optimized protocol to isolate primary mouse peritoneal macrophage metabolites'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS