T4 RNA Ligase (10 U/μL)
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T4 RNA Ligase (10 U/μL)
Thermo Scientific™

T4 RNA Ligase (10 U/μL)

Thermo Scientific T4 RNA Ligase catalyzes the ATP-dependent intra- and intermolecular formation of phosphodiester bonds between 5'-phosphate and 3'-hydroxyl termini자세히 알아보기
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카탈로그 번호수량
EL00211,000 units
카탈로그 번호 EL0021
제품 가격(KRW)
101,000
Online offer
Ends: 31-Dec-2025
118,000
할인액 17,000 (14%)
Each
카트에 추가하기
수량:
1,000 units
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
101,000
Online offer
Ends: 31-Dec-2025
118,000
할인액 17,000 (14%)
Each
카트에 추가하기
Thermo Scientific T4 RNA Ligase catalyzes the ATP-dependent intra- and intermolecular formation of phosphodiester bonds between 5'-phosphate and 3'-hydroxyl termini of oligonucleotides, single-stranded RNA and DNA.

The minimal substrate is a nucleoside 3',5'-biphosphate in intermolecular reaction and oligonucleotide of 8bases in intramolecular reaction.

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

Note

The recommended BSA concentration in the reaction mixture is 0.1mg/mL.
For Research Use Only. Not for use in diagnostic procedures.
사양
함께 사용가능한 버퍼10X Reaction Buffer
제품 유형T4 RNA Ligase
수량1,000 units
농도10 U/μL
효소T4 RNA Ligase
Unit SizeEach

자주 묻는 질문(FAQ)

What are some of the problems associated with sticky-end cloning?

The amplified DNA needs to be purified from the PCR mixture components prior to cloning. The dNTPs carried over from the PCR are competitive inhibitors for ATP in the ligation reaction.

If during synthesis of the PCR primers their chemical integrity has been compromised by either a base substitution or modification, the enzyme recognition site may in actuality not exist. If this is the case, PCR products will be resistant to digestion with restriction enzymes. It may be necessary to use a higher concentration of the restriction enzyme and to incubate at the appropriate temperature overnight to ensure cutting.