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UGT2B10 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | P36537 |
| Other Accession | O97951, O75310, O02663, P16662, NP_001066.1 |
| Reactivity | Human |
| Predicted | Monkey |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 60774 Da |
| Antigen Region | 431-458 aa |
| Gene ID | 7365 |
|---|---|
| Other Names | UDP-glucuronosyltransferase 2B10, UDPGT 2B10, UGT2B10 |
| Target/Specificity | This UGT2B10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 431-458 amino acids from the C-terminal region of human UGT2B10. |
| Dilution | WB~~1:1000 E~~Use at an assay dependent concentration. |
| 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 | UGT2B10 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | UGT2B10 |
|---|---|
| Function | UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. |
| Cellular Location | Microsome membrane; Single-pass membrane protein. Endoplasmic reticulum membrane; Single-pass membrane protein |
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
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds.
References
Chen, G., et al. Cancer Res. 70(19):7543-7552(2010)
Berg, J.Z., et al. Cancer Epidemiol. Biomarkers Prev. 19(6):1423-1431(2010)
Chen, G., et al. Pharmacogenet. Genomics 18(3):181-191(2008)
Chen, G., et al. Cancer Res. 67(19):9024-9029(2007)
Kaivosaari, S., et al. Mol. Pharmacol. 72(3):761-768(2007)
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