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您的位置:首頁 > 產(chǎn)品中心 > 生物試劑 > 酶試劑 > M0094T4 DNA連接酶/T4 DNA Ligase

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產(chǎn)品名稱:

T4 DNA連接酶/T4 DNA Ligase

產(chǎn)品型號: M0094
更新時間: 2017-07-16
描述:BR,1u/ul

BR,1u/ul,帶PEG

BR,5u/ul

BR,5u/ul,帶PEG

BR,30u/ul

BR,30u/ul,帶PEG

產(chǎn)品介紹

 Description
Application 0.01 Weiss unit is the amount of enzyme required to ligate >95% of 1 ug bacteriophage lambda Hind III fragments at 16°C in 20 minutes.
Biochem/physiol Actions T4 DNA Ligase forms an energy dependent phosphodiester linkage between the termini of adjacent polynucleotides of duplex DNA. The ligation reaction requires ATP as a cofactor.1 Ligation of blunt-ended fragments requires higher enzyme concentration and can be facilitated by using PEG in the reaction mixture.2 The enzyme requires a 3′ hydroxyl and 5′ phosphate for ligation. Self-ligation of vector DNA can be prevented by dephosphorylation with alkaline phosphatase. T4 ligase plays an active role in repair of DNA and RNA nicks.3
Features and Benefits • Ligation of blunt ended or cohesive DNA fragments.
• Ligation of cloning vector and restriction insert fragments.
• Seal nicks in double stranded DNA and RNA or DNA/RNA hybrids.
• Couple RNA single strands by bridging oligonucleotide adapters.
 
Other Notes T4 DNA Ligase is inactivated by heating at 65 °C for 10 minutes.
Unit Definition One Weiss unit is defined as the amount of enzyme required to catalyze the exchange of 1 nmole of P32 from pyrophosphate into ATP as Norit-absorbable material in 20 minutes at 37°C. 
Physical form Solution in 10 mM Tris-HCl, pH 7.5, 50 mM KCl, 1 mM DTT, 50% glycerol (v/v)

Properties
form buffered aqueous glycerol solution
concentration 500-6,000 Weiss units/mL
shipped in dry ice
storage temp. −20°C

Safety
Personal Protective Equipment Eyeshields, Gloves, half-mask respirator (EU), half-mask respirator (US), multi-purpose combination respirator cartridge (US)
WGK Germany 3

References
Cited Reference 1. Rusche, J., Hexamine cobalt chloride promotes intermolecular ligation of blunt end DNA fragments by T4 DNA ligase. Nucleic Acids Res. 13, 1997-2008, (1985) Abstract
  2. Upcroft, P., Rapid and efficient method for cloning of blunt-ended DNA fragments. Gene 51, 69-75, (1987) Abstract
  3. Engler, M.J. and Richardson, C.C., Boyer, P.D. The Enzymes San Diego, CA , (1982) 5, 3
reference , Sambrook, J., et al. Molecular Cloning: A Laboratory Manual 2nd ed., Plainview, NY , (1989), 1.53-1.73
  Moore, M.J., Site-specific modification of pre-mRNA: the 2'-hydroxyl groups at the splice sites. Science 256, 992-997, (1992) Abstract

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