GTPBP3 Antibody(Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
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- 实验流程
- 背景知识
Application
| WB, E |
|---|---|
| Primary Accession | Q969Y2 |
| Other Accession | NP_116009.2 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 52058 Da |
| Antigen Region | 293-320 aa |
| Gene ID | 84705 |
|---|---|
| Other Names | tRNA modification GTPase GTPBP3, mitochondrial, GTP-binding protein 3, Mitochondrial GTP-binding protein 1, GTPBP3, MTGP1 |
| Target/Specificity | This GTPBP3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 293-320 amino acids from the Central region of human GTPBP3. |
| 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 | GTPBP3 Antibody(Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | GTPBP3 (HGNC:14880) |
|---|---|
| Synonyms | MTGP1 |
| Function | GTPase component of the GTPBP3-MTO1 complex that catalyzes the 5-taurinomethyluridine (taum(5)U) modification at the 34th wobble position (U34) of mitochondrial tRNAs (mt-tRNAs), which plays a role in mt-tRNA decoding and mitochondrial translation (PubMed:29390138, PubMed:33619562). Taum(5)U formation on mammalian mt-tRNA requires the presence of both GTPBP3-mediated GTPase activity and MTO1 catalytic activity (PubMed:29390138). |
| Cellular Location | Mitochondrion |
| Tissue Location | Ubiquitously expressed. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described.
REFERENCES
Reiling, E., et al. Eur. J. Hum. Genet. 17(8):1056-1062(2009)
Villarroya, M., et al. Mol. Cell. Biol. 28(24):7514-7531(2008)
Bykhovskaya, Y., et al. Mol. Genet. Metab. 83(3):199-206(2004)
Li, X., et al. Biochem. Biophys. Res. Commun. 312(3):747-754(2003)
Li, X., et al. Mol. Cell. Biol. 22(21):7701-7711(2002)
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