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The protein encoded by ECHS1 functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. Additionally we are shipping Enoyl CoA Hydratase, Short Chain, 1, Mitochondrial Proteins (14) and Enoyl CoA Hydratase, Short Chain, 1, Mitochondrial Kits (4) and many more products for this protein.
Showing 10 out of 53 products:
Cow (Bovine) Polyclonal ECHS1 Primary Antibody for WB - ABIN2782325
Takahashi, Watari, Shinya, Shimizu, Takahashi: Suppression of virus replication via down-modulation of mitochondrial short chain enoyl-CoA hydratase in human glioblastoma cells. in Antiviral research 2007
Cow (Bovine) Polyclonal ECHS1 Primary Antibody for WB - ABIN2782327
Bruneel, Labas, Mailloux, Sharma, Royer, Vinh, Pernet, Vaubourdolle, Baudin: Proteomics of human umbilical vein endothelial cells applied to etoposide-induced apoptosis. in Proteomics 2005
Human ECHS1 catalyses the hydration of five substrates via different metabolic pathways, with the highest specificity for crotonyl-CoA and the lowest specificity for tiglyl-CoA
These results suggested that ECHS1 may promote cell proliferation in hepatocellular carcinoma in an EGFR (show EGFR Antibodies)-dependent manner.
In conclusion, the results of the present study suggested that ECHS1 may have an important role in colorectal cancer cell proliferation and migration
identification of four additional patients with mutations in ECHS1 highlights the importance of the valine degradation pathway in Leigh syndrome
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
ECHS1 may play important roles in gastric cancer cell proliferation and migration through PKB (show AKT1 Antibodies)- and GSK3b (show GSK3b Antibodies)-related signaling pathways.
The study demonstrated that ECHS1 mutations result in ECHS1 deficiency and are another cause of Leigh disease in two siblings.
ECHS1 knockdown reduced cell viability and enhanced cisplatin-induced apoptosis in hepatocellular carcinoma cells.
The results confirmed that small hepatitis B surface antigen (SHBs) interacted with ECHS1.
The coexistence of HBs and ECHS1 enhances HepG2 cell apoptosis, affects ECHS1 localization in the mitochondria and induces apoptosis by decreasing the mitochondrial membrane potential (MMP).
potential protein targets for the loss of PostC may include F(1)-ATPase (show DNAH8 Antibodies) gamma, Echs1 and Hsp20 (show HSPB6 Antibodies) that could regulate cellular ATP consumption/production and defense response to ischaemic stress
The protein encoded by this gene functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The gene product is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature.
enoyl Coenzyme A hydratase, short chain, 1, mitochondrial
, enoyl-CoA hydratase 1
, enoyl-CoA hydratase, mitochondrial
, short-chain enoyl-CoA hydratase
, short chain enoyl-CoA hydratase
, Enoyl-CoA hydratase short chain 1 mitochondrial
, Enoyl-CoA hydratase, short chain 1, mitochondrial
, enoyl Coenzyme A hydratase, short chain 1
, mitochondrial short-chain enoyl-coenzyme A hydratase 1