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Browse our anti-ACADL (ACADL) Antibodies

Full name:: anti-Acyl-CoA Dehydrogenase, Long Chain Antibodies (ACADL)

On www.antibodies-online.com are 114 Acyl-CoA Dehydrogenase, Long Chain (ACADL) Antibodies from 21 different suppliers available. Additionally we are shipping ACADL Proteins (9) and ACADL Kits (8) and many more products for this protein. A total of 139 ACADL products are currently listed.

Synonyms:: AA960361, ACAD4, ACOADA, AU018452, C79855, LCAD, zgc:55656

list all antibodies	Gene Name	GeneID	UniProt
	ACADL	33	P28330
	ACADL	25287	P15650
	ACADL	11363	P51174
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Most Popular Reactivities for anti-ACADL (ACADL) Antibodies

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anti-Human ACADL Antibodies:

anti-Rat (Rattus) ACADL Antibodies:

anti-Mouse (Murine) ACADL Antibodies:

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Relevant Pathways for anti-ACADL Antibodies

Monocarboxylic Acid Catabolic Process

More product categories related to ACADL Antibody

Top referenced anti-ACADL Antibodies

Human Polyclonal ACADL Primary Antibody for ELISA, WB - ABIN559742 : Tucci, Herebian, Sturm, Seibt, Spiekerkoetter: Tissue-specific strategies of the very-long chain acyl-CoA dehydrogenase-deficient (VLCAD-/-) mouse to compensate a defective fatty acid ?-oxidation. in PLoS ONE 2012 (PubMed)
Human Polyclonal ACADL Primary Antibody for IHC (p), WB - ABIN652476 : Geillinger, Rathmann, Köhrle, Fiamoncini, Daniel, Kipp: Hepatic metabolite profiles in mice with a suboptimal selenium status. in The Journal of nutritional biochemistry 2014 (PubMed)
Cow (Bovine) Polyclonal ACADL Primary Antibody for WB - ABIN2778159 : Lea, Abbas, Sprecher, Vockley, Schulz: Long-chain acyl-CoA dehydrogenase is a key enzyme in the mitochondrial beta-oxidation of unsaturated fatty acids. in Biochimica et biophysica acta 2000 (PubMed)
Show all 2 Pubmed References

More Antibodies against ACADL Interaction Partners

Human Acyl-CoA Dehydrogenase, Long Chain (ACADL) interaction partners

the fatty acid oxidation pathway and LCAD are factors contributing to the pathophysiology of pulmonary disease
Sirtuin 3 (SIRT3) protein regulates long-chain acyl-CoA dehydrogenase by deacetylating conserved lysines near the active site.
LCAD is minimally expressed in human skeletal muscle and likely does not play a significant role in long-chain fatty acid oxidation.

Mouse (Murine) Acyl-CoA Dehydrogenase, Long Chain (ACADL) interaction partners

LCAD-/- mice succumb to influenza from bioenergetic starvation, likely due to increased reliance upon glucose for energy.
SIRT3 may play an essential role in attenuating lipid accumulation in the heart through the deacetylation of LCAD
Carnitine supplementation lowered myocardial triglycerides, normalizing myocardial triglycerides levels in LCAD Knock-out mice.
LCAD KO mice are ineffective in maintaining metabolic homeostasis during fasting, which is reflected by an impaired myocardial energy status in fasted LCAD KO mice.
the fatty acid oxidation pathway and LCAD are factors contributing to the pathophysiology of pulmonary disease
Sirtuin 3 (SIRT3) protein regulates long-chain acyl-CoA dehydrogenase by deacetylating conserved lysines near the active site.
mice with an inherited deficiency of very long-chain acyl-CoA dehydrogenase (VLCAD), were protected from high-fat diet-induced obesity and liver and muscle insulin resistance.
LCAD is deacetylated in wild-type mice under fasted conditions and by SIRT3 in vitro and in vivo; hyperacetylation of LCAD reduces its enzymatic activity
These data demonstrate that primary defects in mitochondrial fatty acid oxidation capacity can lead to diacylglycerol accumulation, PKCepsilon activation, and hepatic insulin resistance.
Novel candidate genes in T1D CD55 and Acadl were identified.
substantial cardiac hypertrophy in LCAD-deficient mice

ACADL Antigen Profile

Antigen Summary

The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

Alternative names and synonyms associated with ACADL

acyl-CoA dehydrogenase long chain (acadl) antibody
acyl-CoA dehydrogenase long chain (ACADL) antibody
acyl-CoA dehydrogenase, long chain (acadl) antibody
acyl-CoA dehydrogenase, long chain (Acadl) antibody
acyl-CoA dehydrogenase, long chain L homeolog (acadl.L) antibody
acyl-CoA dehydrogenase, long chain (ACADL) antibody
acyl-Coenzyme A dehydrogenase, long-chain (Acadl) antibody

AA960361 antibody
ACAD4 antibody
ACOADA antibody
AU018452 antibody
C79855 antibody
LCAD antibody
zgc:55656 antibody

Protein level used designations for ACADL

LCAD , long-chain specific acyl-CoA dehydrogenase, mitochondrial , acyl-Coenzyme A dehydrogenase, long chain , long-chain acyl-CoA dehydrogenase , Acyl Coenzyme A dehydrogenase, long chain , LCAD long chain acyl-CoA dehydrogenase , acetyl-Coenzyme A dehydrogenase, long-chain , acyl-Coenzyme A dehydrogenase, long-chain

GENE ID	SPECIES
394156	Danio rerio
459914	Pan troglodytes
734116	Xenopus (Silurana) tropicalis
33	Homo sapiens
396931	Sus scrofa
614508	Bos taurus
25287	Rattus norvegicus
446669	Xenopus laevis
424005	Gallus gallus
478895	Canis lupus familiaris
11363	Mus musculus

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Show all anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) Antibodies with Pubmed References

Human Acyl-CoA Dehydrogenase, Long Chain (ACADL) interaction partners

Mouse (Murine) Acyl-CoA Dehydrogenase, Long Chain (ACADL) interaction partners

Antigen Summary

Alternative names and synonyms associated with ACADL

Protein level used designations for ACADL