Code No. | RN019M | |
Anti-2,2,7-trimethylguanosine (m3G/TMG) mAb | ||
Size | 200 µL (1 mg/mL) | |
Availability (in Japan) | 10 or more
(In Japan at 00:05, Oct 9, 2024 in JST) |
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Clonality | Monoclonal | |
Clone | 235-1 | |
Isotype (Immunized Animal) |
Mouse IgG2aκ | |
Applications | IP 10 µg/sample IC 0.5-1 µg/mL |
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Immunogen (Antigen) |
Carrier protein-conjugated trimethylguanosine (m3G/TMG) | |
Storage buffer | 1 mg/mL in PBS/50% glycerol, pH 7.2 | |
Storage temp. | -20°C | |
Conjugate | Unlabeled | |
Manufacturer | MBL | |
Alternative names | N2,N2,7-Trimethylguanosine, m2,2,7G | |
Background | Small nuclear RNA (snRNA) is known to be involved in pre-mRNA splicing as an RNA component of snRNP. 2,2,7-trimethylated guanosine (m3G/TMG) is a modified nucleoside at the 5’-cap site of U snRNAs except for U6 snRNA. Shortly after transcription, 7-methylguanosine (m7G), called cap structure, is added to 5’-end of newly synthesized U snRNA and m7G-capped U snRNA is exported to the cytoplasm. The m7G-cap is converted to m3G-cap, which is a hypermethylated structure of 5’-end, by cytoplasmic catalytic protein TSG1 and the m3G-capped U snRNA forms snRNP with Sm proteins in the cytoplasm, followed by entry into the nucleus. The m3G-capped snRNP plays a role in regulation of pre-mRNA splicing as a part of spliceosome in nucleus. It is also reported that U3 and U8 snoRNA, localized to Cajal body during RNP biogenesis, possess m3G-cap structure. | |
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Product category | Research area:RNA-RNP Network Epigenetics Brands:RiboCluster Profiler™ |
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Data | ||
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