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Choline Acetyltransferase/CHAT Rabbit Polyclonal Antibody

CAT: 0013-GTR17690610Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17690610Size:100 µg
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Description
Choline Acetyltransferase/CHAT Rabbit Polyclonal Antibody
Product Name Alternative
Choline O-acetyltransferase; CHOACTase; ChAT; Choline acetylase; 2.3.1.6; CHAT
UniProt
P28329
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
E.coli-derived human CHAT recombinant protein (Position: D446-R652) . Human CHAT shares 88.4% and 87% amino acid (aa) sequence identity with mouse and rat CHAT, respectively.
Target
Choline O-acetyltransferase
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Disease Biomarkers, Neuroscience, Pharmacology & Drug Discovery
Purification
Immunogen affinity purified.
Concentration
Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Dilution
Immunohistochemistry (Paraffin-embedded Section), 0.5-1μg/ml, Mouse, Rat, Human Western blot, 0.1-0.5μg/ml, Mouse, Rat, Human
Form
Lyophilized
Molecular Weight
83 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
IHC, WB
Host or Source
Rabbit
Preservative
Each vial contains 4mg Trehalose, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3.
Isotype
Rabbit IgG

UniProtKB · P28329

Choline O-acetyltransferase

CLAT_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P28329
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CHAT
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
CHOACTase, ChAT, Choline acetylase
EC number
2.3.1.6
Processing
—
Secondary accessions
A2BDF4, A2BDF5, Q16488, Q9BQ23, Q9BQ35, Q9BQE1
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Molecular function

AcyltransferaseTransferase

Coding sequence diversity

Alternative splicing

Disease

Congenital myasthenic syndromeDisease variant

Biological process

Neurotransmitter biosynthesis

PTM

Phosphoprotein

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