BCHE cDNA
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In stock
SKU
ATGD0421
Description
BCHE belongs to the type-B carboxylesterase/lipase family. Mutant alleles at the BCHE locus are responsible for suxamethonium sensitivity. Defects in BCHE are the cause of butyrylcholinesterase deficiency (BChE deficiency). BChE deficiency is a metabolic disorder characterized by prolonged apnoea after the use of certain anesthetic drugs, including the muscle relaxants succinylcholine or mivacurium and other ester local anestheticsAlternative Names
CHE1, CHE2, E1, Butyrylcholinesterase, Cholinesterase 1Concentration
LyophilizedStorage: Store the plasmid at -20C.
BCHE belongs to the type-B carboxylesterase/lipase family. Mutant alleles at the BCHE locus are responsible for suxamethonium sensitivity. Defects in BCHE are the cause of butyrylcholinesterase deficiency (BChE deficiency). BChE deficiency is a metabolic disorder characterized by prolonged apnoea after the use of certain anesthetic drugs, including the muscle relaxants succinylcholine or mivacurium and other ester local anestheticsAlternative Names
CHE1, CHE2, E1, Butyrylcholinesterase, Cholinesterase 1Concentration
LyophilizedStorage: Store the plasmid at -20C.
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