Product: Tebanicline (hydrochloride)
FACL4 Antibody Summary
| Immunogen |
Recombinant protein encompassing a sequence within the center region of human FACL4. The exact sequence is proprietary.
|
| Localization |
Mitochondrion outer membrane; Single-pass type III membrane protein; Peroxisome membrane; Microsome membrane; Endoplasmic reticulum membrane
|
| Predicted Species |
Mouse (93%), Rat (94%), Porcine (94%), Rhesus Macaque (99%). Backed by our 100% Guarantee.
|
| Isotype |
IgG
|
| Clonality |
Polyclonal
|
| Host |
Rabbit
|
| Gene |
ACSL4
|
| Purity |
Immunogen affinity purified
|
| Innovators Reward |
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|
Applications/Dilutions
| Dilutions |
|
| Application Notes |
The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
|
| Theoretical MW |
79 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
Packaging, Storage & Formulations
| Storage |
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
|
| Buffer |
0.1M Tris (pH 7.0), 0.1M Glycine and 20% Glycerol
|
| Preservative |
0.01% Thimerosal
|
| Concentration |
0.25 mg/ml
|
| Purity |
Immunogen affinity purified
|
Alternate Names for FACL4 Antibody
- 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
Background
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq]