Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : EMQZ1417
| Cat. No. | EMQZ1417 |
| Description | T4 RNA Ligase catalyzes the formation of a phosphodiester bond between a 5´-phosphoryl-terminated nucleic acid donor and a 3´-hydroxyl-terminated nucleic acid acceptor in a template-independent manner. The enzyme is ATP-dependent, and is active on a broad range of substrates including RNA, DNA, oligoribonucleotides, oligodeoxyribonucleotides, as well as numerous nucleotide derivatives. |
| Source | E. coli strain |
| Concentration | 10,000 U/ml |
| Applications |
• " • RNA 3'-end labeling with cytidine 3',5'-bis [alpha-32P] phosphate • Joining RNA to RNA • Synthesis of oligoribonucleotides and oligodeoxyribonucleotides • Specific modifications of tRNAs • Oligodeoxyribonucleotide ligation to single-stranded cDNAs for 5' RACE (Rapid Amplification of cDNA Ends) • Site-specific generation of composite primers for PCR" |
| Size | 500 U; 5,000 U |
| Storage | Store at -20°C |
A: Yes, the enzyme is ATP-dependent.
A: T4 RNA Ligase can be used to connect RNA to RNA, RNA to DNA, and DNA to DNA. However, the efficiency of the latter two connections is low.
A: Generally, the reaction is performed at 16°C for 2 hours or overnight.
A: The expression gene of the enzyme comes from T4 phage, and the enzyme is expressed and purified from E. coli.
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The ligase has activity on a wide range of substrates, including RNA, DNA, oligonucleotides, deoxyoligonucleotides, and many nucleotide derivatives.
Generally, the reagents can be received within a week.
T4 RNA Ligase can be used to generate site-specifically modified RNAs, especially oligonucleotide modifications and anticodon tRNA modifications.
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