GTX89766-PEP
FACL4 blocking peptide
Cannot supply to this region.
- SKU:
- GTX89766-PEP
- Additional Names:
- Acyl-Coa Synthetase Long Chain Family Member 4 , Acs4 , Facl4 , Lacs4 , Mrx63 , Mrx68 , Acsl4
- Physical State:
- Lyophilized
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Buffer:
- Reconstitute with 200ul distilled water to obtain a 0.5mg/ml peptide solution. Lyophilized from 5% (v/v) acetonitrile/H₂O, no preservatives.
- Immunogen:
- acyl-CoA synthetase long-chain family member 4
- Species:
- Human
- Synonyms:
- ACS4;acyl-CoA synthetase 4;arachidonate--CoA ligase;FACL4;fatty-acid-Coenzyme A ligase, long-chain 4;LACS4;lignoceroyl-CoA synthase;long-chain acyl-CoA synthetase 4;long-chain fatty-acid-Coenzyme A ligase 4;long-chain-fatty-acid--CoA ligase 4;MRX63;MRX68;XLID63
- Extra Details:
- 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, Jul 2008]
- Shipping Conditions:
- Blue Ice