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Neuroscience Neurotransmitter Acetylcholine

Butyrylcholinesterase Assay Kit (ab241010)

Price and availability

405 398 ₸

Availability

Order now and get it on Thursday February 25, 2021

Butyrylcholinesterase Assay Kit (ab241010)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Detection method: Colorimetric
  • Platform: Microplate reader

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Overview

  • Product name

    Butyrylcholinesterase Assay Kit
    See all Butyrylcholinesterase kits
  • Detection method

    Colorimetric
  • Product overview

    Butyrylcholinesterase Assay Kit (ab241010) is based on the ability of Butyrylcholinesterase (BChE) to hydrolyze substrate and produce thiocholine. Thiocholine reacts with 5, 5’-dithiobis (2-nitrobenzoic acid) (DTNB) and generates a yellow chromophore that can be quantified at 412 nm. The assay is simple, sensitive and can detect as low as 0.2 U/ml in variety of samples.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 100 tests
    BChE Assay Buffer 1 x 50ml
    BChE Substrate (in DMSO) 1 x 100µl
    Butyrylcholinesterase 1 vial
    DTNB 1 vial
    TNB Standard 1 vial
  • Research areas

    • Neuroscience
    • Neurotransmitter
    • Acetylcholine
    • Neuroscience
    • Neurology process
    • Neurodegenerative disease
    • Alzheimer's disease
    • Other
    • Signal Transduction
    • Metabolism
    • Drug metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Drug metabolism
    • Metabolism
    • Types of disease
    • Neurodegenerative disease
  • Function

    Esterase with broad substrate specificity. Contributes to the inactivation of the neurotransmitter acetylcholine. Can degrade neurotoxic organophosphate esters.
  • Tissue specificity

    Detected in blood plasma (at protein level). Present in most cells except erythrocytes.
  • Involvement in disease

    Defects in BCHE are the cause of butyrylcholinesterase deficiency (BChE deficiency) [MIM:177400]. 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. The duration of the prolonged apnoea varies significantly depending on the extent of the enzyme deficiency. BChE deficiency is a multifactorial disorder. The hereditary condition is transmitted as an autosomal recessive trait.
  • Sequence similarities

    Belongs to the type-B carboxylesterase/lipase family.
  • Cellular localization

    Secreted.
  • Target information above from: UniProt accession P06276 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Alternative names

    • Acylcholine acylhydrolase
    • BCHE
    • Butyrylcholine esterase
    • CHE1
    • CHE2
    • CHLE_HUMAN
    • Choline esterase II
    • Cholinesterase
    • Cholinesterase (serum) 2
    • Cholinesterase 1
    • E1
    • Pseudocholinesterase
    • Pseudocholinesterase E1
    see all

Images

  • TNB standard curve
    TNB standard curve

    TNB standard curve

  • BChE activity
    BChE activity

    BChE activity in Human Blood (10 µL, 1:100 dilution), Human Serum (10 µL, 1:50 dilution) and Human Plasma (10 µL, 1:50 dilution).

  • BChE activity
    BChE activity

    BChE activity in Rat Liver (30 µg protein) and Rat Lung (15 µg protein). Assays were performed following the kit protocol.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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