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USP17L3 Antibody - C-terminal region
Rabbit Polyclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB |
|---|---|
| Primary Accession | A6NCW0 |
| Other Accession | NM_001256871, NP_001243800 |
| Reactivity | Human |
| Predicted | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 59kDa |
| Gene ID | 645836 |
|---|---|
| Alias Symbol | USP17B, USP17F |
| Other Names | Ubiquitin carboxyl-terminal hydrolase 17-like protein 3, 3.4.19.12, Deubiquitinating enzyme 17-like protein 3, Ubiquitin thioesterase 17-like protein 3, Ubiquitin-specific-processing protease 17-like protein 3, USP17L3, USP17B, USP17F |
| Format | Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose. |
| Reconstitution & Storage | Add 50 &mu, l of distilled water. Final Anti- antibody concentration is 1 mg/ml in PBS buffer with 2% sucrose. For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles. |
| Precautions | USP17L3 Antibody - C-terminal region is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | USP17L3 |
|---|---|
| Synonyms | USP17B, USP17F |
| Function | Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes that may include cell proliferation, progression through the cell cycle, apoptosis, cell migration, and the cellular response to viral infection. |
| Cellular Location | Nucleus. Endoplasmic reticulum |
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
Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes that may include cell proliferation, progression through the cell cycle, apoptosis, cell migration, and the cellular response to viral infection.
References
Nusbaum C.,et al.Nature 439:331-335(2006).
Burrows J.F.,et al.Genomics 85:524-529(2005).
Shin J.-M.,et al.BMC Genomics 7:292-292(2006).
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