UGT2A3 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
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Primary Accession | Q6UWM9 |
Other Accession | NP_079019.3 |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 60254 Da |
Antigen Region | 324-353 aa |
Gene ID | 79799 |
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Other Names | UDP-glucuronosyltransferase 2A3, UDPGT 2A3, UGT2A3 |
Target/Specificity | This UGT2A3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 324-353 amino acids from the Central region of human UGT2A3. |
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 | UGT2A3 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | UGT2A3 |
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Function | UDP-glucuronosyltransferases catalyze phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds (By similarity). |
Cellular Location | Membrane; Single-pass type I membrane protein |
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Provided below are standard protocols that you may find useful for product applications.
Background
UDP-glucuronosyltransferases catalyze phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds (By similarity).
References
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Sneitz, N., et al. Pharmacogenet. Genomics (2009) In press :
Court, M.H., et al. Mol. Pharmacol. 74(3):744-754(2008)
Clark, H.F., et al. Genome Res. 13(10):2265-2270(2003)
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