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POMT2 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | Q9UKY4 |
| Other Accession | Q8BGQ4, NP_037514.2 |
| Reactivity | Human |
| Predicted | Mouse |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 84214 Da |
| Antigen Region | 540-567 aa |
| Gene ID | 29954 |
|---|---|
| Other Names | Protein O-mannosyl-transferase 2, Dolichyl-phosphate-mannose--protein mannosyltransferase 2, POMT2 |
| Target/Specificity | This POMT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 540-567 amino acids from the C-terminal region of human POMT2. |
| 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 | POMT2 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | POMT2 |
|---|---|
| Function | Transfers mannosyl residues to the hydroxyl group of serine or threonine residues. Coexpression of both POMT1 and POMT2 is necessary for enzyme activity, expression of either POMT1 or POMT2 alone is insufficient (PubMed:14699049, PubMed:28512129). Essentially dedicated to O-mannosylation of alpha-DAG1 and few other proteins but not of cadherins and protocaherins (PubMed:28512129). |
| Cellular Location | Endoplasmic reticulum membrane; Multi-pass membrane protein |
| Tissue Location | Highly expressed in testis; detected at low levels in most tissues |
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
The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS).
References
Manya, H., et al. J. Biochem. 147(3):337-344(2010)
Yanagisawa, A., et al. Eur J Med Genet 52(4):201-206(2009)
Murakami, T., et al. Brain Dev. 31(6):465-468(2009)
Mercuri, E., et al. Neurology 72(21):1802-1809(2009)
Messina, S., et al. Neuromuscul. Disord. 18(7):565-571(2008)
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