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COLQ Antibody(C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | Q9Y215 |
| Other Accession | O35167, O35348, NP_536800.2 |
| Reactivity | Human, Mouse |
| Predicted | Rat |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 47766 Da |
| Antigen Region | 324-353 aa |
| Gene ID | 8292 |
|---|---|
| Other Names | Acetylcholinesterase collagenic tail peptide, AChE Q subunit, Acetylcholinesterase-associated collagen, COLQ |
| Target/Specificity | This COLQ antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 324-353 amino acids from the C-terminal region of human COLQ. |
| Dilution | WB~~1:1000 |
| Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Storage | 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. |
| Precautions | COLQ Antibody(C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | COLQ |
|---|---|
| Function | Anchors the catalytic subunits of asymmetric AChE to the synaptic basal lamina. |
| Cellular Location | Synapse. |
| Tissue Location | Found at the end plate of skeletal muscle. |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes the subunit of a collagen-like molecule associated with acetylcholinesterase in skeletal muscle. Each molecule is composed of three identical subunits. Each subunit contains a proline-rich attachment domain (PRAD) that binds an acetylcholinesterase tetramer to anchor the catalytic subunit of the enzyme to the basal lamina. Mutations in this gene are associated with endplate acetylcholinesterase deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.
References
Mihaylova, V., et al. Brain 131 (PT 3), 747-759 (2008) :
Schreiner, F., et al. Neuromuscul. Disord. 17(3):262-265(2007)
Ting, A.K., et al. Chem. Biol. Interact. 157-158, 63-70 (2005) :
Dvir, H., et al. EMBO J. 23(22):4394-4405(2004)
Ishigaki, K., et al. Neuromuscul. Disord. 13(3):236-244(2003)
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