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Acyl-CoA synthetase family

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Acyl-CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA. Has some preference toward medium-chain substrates. Plays a role in adipocyte differentiation (By similarity).

Below are the list of possible Acyl-CoA synthetase family products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Acyl-CoA synthetase family member 2

 Acyl-CoA synthetase family member 2 ELISA Kit
 Acyl-CoA synthetase family member 2 Recombinant
 Acyl-CoA synthetase family member 2 Antibody
Also known as Acyl-CoA synthetase family member 2, mitochondrial.
Acyl-CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA. Has some preference toward medium-chain substrates. Plays a role in adipocyte differentiation ().
 acsf2 ELISA Kit
 acsf2 Recombinant
 acsf2 Antibody
 zgc:152887 ELISA Kit
 zgc:152887 Recombinant
 zgc:152887 Antibody
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Acyl-CoA synthetase family member 3

 Acyl-CoA synthetase family member 3 ELISA Kit
 Acyl-CoA synthetase family member 3 Recombinant
 Acyl-CoA synthetase family member 3 Antibody
Also known as Acyl-CoA synthetase family member 3, mitochondrial.
ACSF3: Catalyzes the initial reaction in intramitochondrial fatty acid synthesis, by activating malonate and methylmalonate, but not acetate, into their respective CoA thioester. May have some preference toward very-long-chain substrates. Defects in ACSF3 are the cause of combined malonic and methylmalonic aciduria (CMAMMA). A me
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tabolic disease characterized by malonic and methylmalonic aciduria, with urinary excretion of much larger amounts of methylmalonic acid than malonic acid, in the presence of normal malonyl-CoA decarboxylase activity. Clinical features include coma, ketoacidosis, hypoglycemia, failure to thrive, microcephaly, dystonia, axial hypotonia and/or developmental delay, and neurologic manifestations including seizures, psychiatric disease and/or cognitive decline. Belongs to the ATP-dependent AMP-binding enzyme family.

Protein type: EC 6.-.-.-; EC 6.2.1.-; Ligase

Cellular Component: mitochondrion

Molecular Function: acid-thiol ligase activity

Biological Process: fatty acid biosynthetic process; fatty acid metabolic process
 Acsf3 ELISA Kit
 Acsf3 Recombinant
 Acsf3 Antibody
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Acyl-CoA synthetase family member 4

 Acyl-CoA synthetase family member 4 ELISA Kit
 Acyl-CoA synthetase family member 4 Recombinant
 Acyl-CoA synthetase family member 4 Antibody
Acyl-CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA.
 aasdh ELISA Kit
 aasdh Recombinant
 aasdh Antibody
 acsf4 ELISA Kit
 acsf4 Recombinant
 acsf4 Antibody
 si:dkeyp-117h8.3 ELISA Kit
 si:dkeyp-117h8.3 Recombinant
 si:dkeyp-117h8.3 Antibody
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Acyl-CoA synthetase family member 4 homolog

 Acyl-CoA synthetase family member 4 homolog ELISA Kit
 Acyl-CoA synthetase family member 4 homolog Recombinant
 Acyl-CoA synthetase family member 4 homolog Antibody
Acyl-CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA.
 U26 ELISA Kit
 U26 Recombinant
 U26 Antibody
 CG13401 ELISA Kit
 CG13401 Recombinant
 CG13401 Antibody
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