ARG63748

anti-ACHE antibody

anti-ACHE antibody for Flow cytometry,ICC/IF,Western blot and Human

Neuroscience antibody

Overview

Product Description Goat Polyclonal antibody recognizes ACHE
Tested Reactivity Hu
Predict Reactivity Ms, Rat
Tested Application FACS, ICC/IF, WB
Specificity This antibody is expected to recognise isoform NP_000656 only (the ubiquitously expressed, hydrophillic form).
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name ACHE
Antigen Species Human
Immunogen QFDHYSKQDRCSDL
Conjugation Un-conjugated
Alternate Names ARACHE; Acetylcholinesterase; ACEE; EC 3.1.1.7; AChE; N-ACHE; YT

Application Instructions

Application Suggestion
Tested Application Dilution
FACS10 µg/ml
ICC/IF10 µg/ml
WB0.3 - 1 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 43 Human ACHE

Swiss-port # P22303 Human Acetylcholinesterase

Background Acetylcholinesterase hydrolyzes the neurotransmitter, acetylcholine at neuromuscular junctions and brain cholinergic synapses, and thus terminates signal transmission. It is also found on the red blood cell membranes, where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties, but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene, and the structural diversity in the gene products arises from alternative mRNA splicing, and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain, muscle and other tissues is the hydrophilic species, which forms disulfide-linked oligomers with collagenous, or lipid-containing structural subunits. The other, alternatively spliced form, expressed primarily in the erythroid tissues, differs at the C-terminal end, and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally. [provided by RefSeq, Jul 2008]
Research Area Neuroscience antibody
Calculated MW 68 kDa

Images (3) Click the Picture to Zoom In

  • ARG63748 anti-ACHE antibody ICC/IF image

    Immunofluorescence: Paraformaldehyde fixed U2OS cells permeabilized with 0.15% Triton. Cells were stained with ARG63748 anti-ACHE antibody (green) at 10 µg/ml dilution for 1 hour. DAPI (blue) for nuclear staining. Negative control: Unimmunized goat IgG (green) at 10 µg/ml dilution.

  • ARG63748 anti-ACHE antibody WB image

    Western blot: 35 µg of HepG2 (A), Daudi (B), HeLa (C) and Jurkat (D) cell lysates (in RIPA buffer) stained with ARG63748 anti-ACHE antibody at 1 µg/ml (A, B) and 0.3 µg/ml (C, D) dilutions and incubated at RT for 1 hour.

  • ARG63748 anti-ACHE antibody FACS image

    Flow Cytometry: Paraformaldehyde-fixed HeLa cells permeabilized with 0.5% Triton. Cells were stained with ARG63748 anti-ACHE antibody (blue line) at 10 µg/ml dilution for 1 hour, followed by incubation with Alexa FluorR 488 labelled secondary antibody. IgG control: Unimmunized goat IgG (black line).