ACSL4 Antikörper (AA 28-56)

Produktnummer ABIN7479739

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch ACSL4 in WB und ELISA. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für ACSL4 Antikörper (AA 28-56) (ABIN7479739)

Target: ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ACSL4 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-ACSL4 Antikörper

Bindungsspezifität: AA 28-56

Verwendungszweck: FACL4 Antibody / ACSL4

Kreuzreaktivität (Details): Expected species reactivity: Mouse,Rat

Aufreinigung: Antigen affinity

Immunogen: A portion of amino acids 28-56 from the human protein was used as the immunogen for this FACL4 antibody.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Titration of the FACL4 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Aliquot the FACL4 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu ACSL4

Target: ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

Andere Bezeichnung: FACL4

Hintergrund: 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.

UniProt: O60488