Choline Acetyltransferase antibody (AA 19-612)
Quick Overview for Choline Acetyltransferase antibody (AA 19-612) (ABIN7600421)
Target
See all Choline Acetyltransferase (CHAT) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 19-612
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Purpose
- Anti-Choline Acetyltransferase/Chat Antibody
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Characteristics
- Anti-Choline Acetyltransferase/Chat Antibody (ABIN7600421). Tested in ELISA, IHC, WB applications. This antibody reacts with Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived rat Choline Acetyltransferase/Chat recombinant protein (Position: E19-D612).
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Isotype
- IgG
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Application Notes
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Western blot, 0.25-0.5 μg/mL, Mouse, Rat
Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Mouse, Rat
ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
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Storage
- 4 °C,-20 °C
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Storage Comment
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
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- Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))
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Alternative Name
- Chat
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Background
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Synonyms: Choline O-acetyltransferase (EC:2.3.1.6); CHOACTase; ChAT; Choline acetylase; Chat
Background: Choline acetyltransferase (commonly abbreviated as ChAT, but sometimes CAT) is a transferase enzyme responsible for the synthesis of the neurotransmitter acetylcholine. In humans, the choline acetyltransferase enzyme is encoded by the CHAT gene. 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.
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Molecular Weight
- 71 kDa
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Gene ID
- 290567
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UniProt
- P32738
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Pathways
- Skeletal Muscle Fiber Development
Target
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