This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Designing a Western blot for ACSL4? The guide has the expected band size, antibodies backed by real blot images, the controls to run alongside, and protocols taken from published papers.
Open the ACSL4 Western Blot Guide17 Citations
8 Citations
2 Citations
1 Citations
1 Citations
Facts about Long-chain-fatty-acid--CoA ligase 4.
.
| Human | |
|---|---|
| Gene Name: | ACSL4 |
| Uniprot: | O60488 |
| Entrez: | 2182 |

| Belongs to: |
|---|
| ATP-dependent AMP-binding enzyme family |

ACS4mental retardation, X-linked 68; acyl-CoA synthetase 4; acyl-CoA synthetase long-chain family member 4; EC 6.2.1.3; FACL4long-chain 4; LACS 4; LACS4MRX68; lignoceroyl-CoA synthase; Long-chain acyl-CoA synthetase 4; long-chain fatty-acid-Coenzyme A ligase 4; long-chain-fatty-acid--CoA ligase 4; mental retardation, X-linked 63; MRX63
Mass (kDA):
79.188 kDA

| Human | |
|---|---|
| Location: | Xq23 |
| Sequence: | X; NC_000023.11 (109641335..109733392, complement) |
Mitochondrion outer membrane; Single-pass type III membrane protein. Peroxisome membrane; Single-pass type III membrane protein. Microsome membrane; Single-pass type III membrane protein. Endoplasmic reticulum membrane; Single-pass type III membrane protein. Cell membrane.





PMID: 9598324 by Cao Y., et al. Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4).
PMID: 9480748 by Piccini M., et al. FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.