CHAT monoclonal antibody, clone ABBO-3

Catalog # MAB19891

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Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of SH-SY5Y cell lysate with CHAT monoclonal antibody.

  • Specification

    Product Description

    Rabbit monoclonal antibody raised against synthetic peptide of human CHAT.

    Immunogen

    A synthetic peptide corresponding to human CHAT.

    Host

    Rabbit

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Flow Cytometry (1:50)
    Immunocytochemistry (1:50-1:200)
    Immunofluorescence (1:50-1:200)
    Immunoprecipitation (1:50)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

    Storage Instruction

    Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Cell lysate)

    Western blot analysis of SH-SY5Y cell lysate with CHAT monoclonal antibody.

    Immunocytochemistry

    Immunofluorescence

    Immunoprecipitation

    Flow Cytometry

  • Gene Info — CHAT

    Entrez GeneID

    1103

    Protein Accession#

    P28329

    Gene Name

    CHAT

    Gene Alias

    CMS1A, CMS1A2

    Gene Description

    choline acetyltransferase

    Omim ID

    118490 254210

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer disease. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq

    Other Designations

    OTTHUMP00000019583|OTTHUMP00000019584|acetyl CoA:choline O-acetyltransferase

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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