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Choline Acetyltransferase antibody

This Rabbit Monoclonal antibody specifically detects Choline Acetyltransferase in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7266343

Quick Overview for Choline Acetyltransferase antibody (ABIN7266343)

Target

See all Choline Acetyltransferase (CHAT) Antibodies
Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

Reactivity

  • 77
  • 50
  • 44
  • 17
  • 4
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 72
  • 7
  • 4
  • 4
  • 3
Rabbit

Clonality

  • 72
  • 18
Monoclonal

Conjugate

  • 49
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Choline Acetyltransferase antibody is un-conjugated

Application

  • 51
  • 32
  • 22
  • 22
  • 22
  • 19
  • 13
  • 13
  • 11
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Purpose

    CHAT Rabbit mAb

    Cross-Reactivity

    Human

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human CHAT

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

    Alternative Name

    CHAT

    Background

    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's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. 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, May 2010],CHAT;CHOACTASE;CMS1A;CMS1A2;CMS6,Cell Type Marker,Cell Type Marker_Neuron marker,Neuroscience,CHAT

    Molecular Weight

    82kDa

    Gene ID

    1103

    UniProt

    P28329

    Pathways

    Skeletal Muscle Fiber Development
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