Ad
related to: carnitine cpt2topsupplements.com has been visited by 10K+ users in the past month
- Top Sports Supplements
Sports Supplements Top Ten Lists
We Review Them So You Get The Best
- Contact Us
We Are Just a Contact Form & Email
Away, Experts Are Here To Help!
- Whey Protein Supplement
Skip the Review, View on Amazon
See the #1 Protein On Amazon.com
- #1 Ranked BCAAs on Amazon
Save Time, Save Money. Amazon.com
The Best BCAA Powder on Amazon.com
- Top Sports Supplements
Search results
Results from the WOW.Com Content Network
Carnitine palmitoyltransferase II deficiency, sometimes shortened to CPT-II or CPT2, is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source. The disorder presents in one of three ...
Carnitine palmitoyltransferase II precursor (CPT2) is a mitochondrial membrane protein which is transported to the mitochondrial inner membrane. CPT2 together with carnitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria.
Carnitine palmitoyltransferase I (CPT1) also known as carnitine acyltransferase I, CPTI, CAT1, CoA:carnitine acyl transferase (CCAT), or palmitoylCoA transferase I, is a mitochondrial enzyme responsible for the formation of acyl carnitines by catalyzing the transfer of the acyl group of a long-chain fatty acyl-CoA from coenzyme A to l-carnitine.
CPT2 may refer to: Carnitine palmitoyltransferase II, an important metabolic enzyme. Carnitine palmitoyltransferase II deficiency, a condition that prevents the body from converting certain fats into energy; Killarney Airport, CPT2 ICAO airport code, located in Killarney, Ontario, Canada
Carnitine O-palmitoyltransferase (also called carnitine palmitoyltransferase) is a mitochondrial transferase enzyme (EC 2.3.1.21) involved in the metabolism of palmitoylcarnitine into palmitoyl-CoA. A related transferase is carnitine acyltransferase .
Carnitine is a quaternary ammonium compound involved in metabolism in most mammals, plants, ... (also called carnitine palmitoyltransferase 2, CPT2), which is located ...
Carnitor - an L-carnitine supplement that has shown to improve the body's metabolism in individuals with low L-carnitine levels. It is only useful for Specific fatty-acid metabolism disease. It is only useful for Specific fatty-acid metabolism disease.
Carnitine palmitoyltransferase II deficiency (also known as CPT-II deficiency) leads to an excess long chain fatty acids, as the body lacks the ability to transport fatty acids into the mitochondria to be processed as a fuel source. [75] The disease is caused by a defect in the gene CPT2. [76]
Ad
related to: carnitine cpt2topsupplements.com has been visited by 10K+ users in the past month