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MRPL18 Antibody (Center) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q9H0U6 |
|---|---|
| Clone Names | 80902035 |
| Gene ID | 29074 |
|---|---|
| Other Names | 39S ribosomal protein L18, mitochondrial, L18mt, MRP-L18, MRPL18 |
| Target/Specificity | The synthetic peptide sequence used to generate the antibody AP7320c was selected from the Center region of human MRPL18. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | MRPL18 |
|---|---|
| Function | Together with thiosulfate sulfurtransferase (TST), acts as a mitochondrial import factor for the cytosolic 5S rRNA. The precursor form shows RNA chaperone activity; is able to fold the 5S rRNA into an import-competent conformation that is recognized by rhodanese (TST). Both the cytoplasmic and mitochondrial forms are able to bind to the helix IV-loop D in the gamma domain of the 5S rRNA. |
| Cellular Location | Mitochondrion |
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Provided below are standard protocols that you may find useful for product applications.
Background
MRPL18 is encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology.
References
Zhang,Z. and Gerstein,M. Genomics 81 (5), 468-480 (2003)Koc,E.C., Burkhart,W. J. Biol. Chem. 276 (47), 43958-43969 (2001)Kenmochi,N., Suzuki,T. Genomics 77 (1-2), 65-70 (2001)
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