BCHE cDNA
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 anesthetics
Product Specifications
Product Name Alternative
CHE1, CHE2, E1, Butyrylcholinesterase, Cholinesterase 1
Chromosomal Location
3q26.1-q26.2
Antigen Species
Human
Vector Type
PATGen (puc19-derived cloning vector)
Sequence
Additionnal Information
Storage Conditions
Store the plasmid at -20C.
Formulation
Lyophilized
Scientific Category
Metabolism
Omim
177400
NCBI Accession Number
NP_000046.1
Species
Human
Preparation
RNA Reference
NM_000055.2
DNA Size
1809bp
Vector Description
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