TEMA RICERCA

Descrizione	Azione
ACSL4/FACL4 Antibody detects endogenous levels of total ACSL4/FACL4. ACSL4/FACL4 Antibody Codice: DF12141 Confezionamento: 200ul	Dettagli
ACSL4/FACL4 Antibody detects endogenous levels of total ACSL4/FACL4. ACSL4/FACL4 Antibody Codice: DF12141 Confezionamento: 100ul	Dettagli
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. ACSL4 Polyclonal Antibody Codice: E-AB-14661_60μL Confezionamento: 60μL	Dettagli
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. ACSL4 Polyclonal Antibody Codice: E-AB-14661_120μL Confezionamento: 120μL	Dettagli
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. ACSL4 Polyclonal Antibody Codice: E-AB-14661_20μL Confezionamento: 20μL	Dettagli
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. ACSL4 Polyclonal Antibody Codice: E-AB-14661_200μL Confezionamento: 200μL	Dettagli
ACSL5 Antibody detects endogenous levels of total ACSL5. ACSL5 Antibody Codice: DF9607 Confezionamento: 200ul	Dettagli
ACSL5 Antibody detects endogenous levels of total ACSL5. ACSL5 Antibody Codice: DF9607 Confezionamento: 100ul	Dettagli
ACSL6 Antibody detects endogenous levels of total ACSL6. ACSL6 Antibody Codice: DF4142 Confezionamento: 200ul	Dettagli
ACSL6 Antibody detects endogenous levels of total ACSL6. ACSL6 Antibody Codice: DF4142 Confezionamento: 100ul	Dettagli
ACSM3 Antibody detects endogenous levels of total ACSM3. ACSM3 Antibody Codice: DF12808 Confezionamento: 100ul	Dettagli
ACSM3 Antibody detects endogenous levels of total ACSM3. ACSM3 Antibody Codice: DF12808 Confezionamento: 200ul	Dettagli

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