ACHE Human
Source:HEK293 Cells.Physical Appearance:Sterile Filtered colorless solution.Biological ActivitySpecific activity is > 6,000 nmol/min/ug. Defined by the amount of enzyme that cleaves 1 nmole of acetylthiocholine per minute at pH 7.5 at 25°C.Acetylcholinesterase (ACHE) belongs to the type-B carboxylesterase/lipase family. ACHE catalyzes the breakdown of acetylcholine and other choline esters that play a role as neurotransmitters. During neurotransmission, ACH is released from the presynaptic neuron into the synaptic cleft and binds ACH receptors on the post-synaptic membrane, transmitting the signal from the nerve. ACHE is located on the post-synaptic membrane, terminates the signal transmission by hydrolyzing ACH.ACHE Human Recombinant produced in HEK cells is a single, glycosylated, polypeptide chain (32-614 a.a) containing a total of 592 amino acids, having a molecular mass of 65.6 kDa. ACHE is fused to a 6 amino acid His-tag at C-terminus, and is purified by proprietary chromatographic techniques.
Product Specifications
Product Name Alternative
AChE, ACEE, ACES_HUMAN, Acetylcholinesterase, ACHE, ARACHE, N-ACHE, VT, Acetylcholinesterase isoform E4-E6
Purification
Greater than 95.0% as determined by SDS-PAGE.
Format
The ACHE solution (0.25mg/mL) contains 10% Glycerol and Phosphate-Buffered Saline (pH 7.4) .
Storage Conditions
Amino Acids
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