Choline Acetyltransferase/ChAT Antibody - Azide and BSA Free Summary
| Immunogen |
A synthetic peptide from mouse Choline Acetyltransferase/ChAT conjugated to blue carrier protein was used as the antigen. The peptide is homologous in rat and human. |
| Marker |
Cholinergic Neuronal Marker |
| Isotype |
IgG |
| Clonality |
Polyclonal |
| Host |
Sheep |
| Gene |
CHAT |
| Purity |
Ammonium sulfate precipitation |
| Innovator's Reward |
Test in a species/application not listed above to receive a full credit towards a future purchase. |
Applications/Dilutions
| Dilutions |
- Immunohistochemistry 10-50 ug/ml
- Immunohistochemistry-Frozen 10-50 ug/ml
- Immunohistochemistry-Paraffin 10-50 ug/ml
- Western Blot 10-50 ug/ml
|
Reactivity Notes
Packaging, Storage & Formulations
| Storage |
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
| Buffer |
Lyophilized from PBS |
| Preservative |
No Preservative |
| Concentration |
LYOPH |
| Purity |
Ammonium sulfate precipitation |
| Reconstitution Instructions |
Reconstitute 0.5 mg size in 0.5 ml of sterile water. Centrifuge to remove any insoluble material. Glycerol may be added (1:1) for additional stability. Please note the 0.1 mg size is provided in reconstituted format. |
Alternate Names for Choline Acetyltransferase/ChAT Antibody - Azide and BSA Free
Background
Cholinergic systems are implicated in numerous neurologic functions. Alteration in some cholinergic neurons may account for the disturbances of Alzheimer disease. The protein encoded by this gene synthesizes the neurotransmitter acetylcholine. Alternative splice variants have been found that contain alternative 5' untranslated exons. Three of the four described splice variants encode identical 69 kDa proteins while one variant encodes both the 69 kDa and a larger 82 kDa protein.; Choline acetylase catalyzes the reversible synthesis of acetylcholine (ACh) from acetyl CoA and choline at cholinergic synapses.; CATALYTIC ACTIVITY: Acetyl-CoA + choline = CoA + O-acetylcholine.; Defects in CHAT are the cause of familial infantile myasthenia gravis 2 (FIMG2); also known as CMS-EA. FIMG2 patients have myasthenic symptoms since birth or early infancy, negative tests for anti-AChR antibodies, and abrupt episodic crises with increased weakness, bulbar paralysis, and apnea precipitated by undue exertion, fever, or excitement. Inheritance is autosomal recessive.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are
guaranteed for 1 year from date of receipt.
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