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anti-Human ACAA2 Anticorps:
anti-Rat (Rattus) ACAA2 Anticorps:
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Human Monoclonal ACAA2 Primary Antibody pour IF, IHC (p) - ABIN564548
Kuhlow, Zarse, Voigt, Schulz, Petzke, Schomburg, Pfeiffer, Ristow: Opposing effects of dietary sugar and saturated fat on cardiovascular risk factors and glucose metabolism in mitochondrially impaired mice. dans European journal of nutrition 2010
Cow (Bovine) Polyclonal ACAA2 Primary Antibody pour WB - ABIN2783320
Aboulaich, Vainonen, Strålfors, Vener: Vectorial proteomics reveal targeting, phosphorylation and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes. dans The Biochemical journal 2004
Show all 2 Pubmed References
Exposure to bezafibrate (400 muM for 48 h) increased the abundance of HADHA (Montrer HADHA Anticorps) and HADHB (Montrer HADHB Anticorps) mRNAs.
nonstructural protein 5 (Montrer CAPS Anticorps) (NS5 (Montrer RAF1 Anticorps)) interacted with hydroxyacyl-CoA dehydrogenase (Montrer HADH Anticorps) alpha and beta subunits, two components of the mitochondrial trifunctional protein (MTP) involved in LCFA beta-oxidation
Mutations in HADHB, which encodes the beta-subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathy.
Heterozygous mutation in HADHB (Montrer HADHB Anticorps) gene cause early-onset axonal axonal Charcot-Marie-tooth disease.
The results demonstrated that ERbeta (Montrer ESR2 Anticorps) was indeed associated and colocalized with HADHB (Montrer HADHB Anticorps) within mitochondria.
HADHB (Montrer HADHB Anticorps) is a functional molecular target of estrogen receptor alpha (Montrer ESR1 Anticorps) in the mitochondria, and the interaction may play an important role in the estrogen-mediated lipid metabolism in animals and humans.
mutational analysis of the HADHB (Montrer HADHB Anticorps) gene, which encodes long-chain 3-ketoacyl-CoA thiolase (Montrer HADHB Anticorps), identified compound heterozygous mutations of c.520C>T (p.R141C) and c.1331G>A (p.R411K) in a case of mitochondrial trifunctional protein deficiency
Results emphasize the value of cDNA analysis in the characterization of HADHA (Montrer HADHA Anticorps) and HADHB (Montrer HADHB Anticorps) mutations and further strengthen the model of haploinsufficiency as a major pathomechanism in MTP defects.
Recombinant mitochondrial trifunctional protein displayed 2-enoyl-CoA hydratase, l-3-hydroxyacyl-CoA dehydrogenase, and 3-ketoacyl-CoA thiolase (Montrer HADHB Anticorps) activities.
The present findings showed that all missense mutations in HADHB (Montrer HADHB Anticorps) were disease-causing.
Data show that the major mitochondrial partner of Shc (Montrer SHC1 Anticorps) adaptor protein p46Shc is the lipid oxidation enzyme 3-ketoacylCoA thiolase (Montrer HADHB Anticorps) ACAA2, to which p46Shc binds directly and with a strong affinity.
The encoded protein catalyzes the last step of the mitochondrial fatty acid beta-oxidation spiral. Unlike most mitochondrial matrix proteins, it contains a non-cleavable amino-terminal targeting signal.
3-ketoacyl-CoA thiolase, mitochondrial
, acetyl-Coenzyme A acyltransferase 2
, beta ketothiolase
, mitochondrial 3-oxoacyl-CoA thiolase
, mitochondrial 3-oxoacyl-Coenzyme A thiolase
, acetyl-Coenzyme A acyltransferase 2 (mitochondrial 3-oxoacyl-Coenzyme A thiolase)
, mitochondrial acetyl-Coenzyme A acyltransferase 2
, acetyl-coenzyme A acyltransferase 2
, acetyl-CoA acyltransferase