產品簡介
T4 DNA連接酶在具有3'羥基和5'磷酸末端的雙鏈DNA之間的ATP存在下催化磷酸二酯鍵的形成。*的T4 DNA連接酶緩沖液可優化連接,可在5分鐘內完成.
蘇州螞蟻淘生物科技有限公司 |
—— 銷售熱線 ——
18915418616 |
Invitrogen抗體|thermo46300018*
描述
T4 DNA連接酶在具有3'羥基和5'磷酸末端的雙鏈DNA之間的ATP存在下催化磷酸二酯鍵的形成。*的T4 DNA連接酶緩沖液可優化連接,可在5分鐘內完成。單鏈核酸不是該酶的底物。提供T4 DNA連接酶技術公告。
應用:克隆(鈍端或粘性末端連接)。將接頭或接頭添加到平端DNA。
來源:從大腸桿菌中純化 - 溶原菌NM989。
性能和質量測試:內切脫氧核糖核酸酶,3'和5'外切脫氧核糖核酸酶測定;結扎效率測試。
單位定義:一個單位催化在20分鐘內將1nmol 32P標記的焦磷酸鹽交換成ATP。在37°C。 (一個單位相當于大約300個粘性末端結扎單位。)
單位反應條件:66mM Tris-HCl(pH 7.6),6.6mM MgCl 2,10mM DTT,66μMATP,3.3μM32P標記的焦磷酸鹽和0.1ml的酶,持續20分鐘。在37°C。
Invitrogen抗體|thermo46300018*
T4 DNA Ligase catalyzes the formation of phosphodiester bonds in the presence of ATP between double-stranded DNAs with 3´ hydroxyl and 5´ phosphate termini. The unique T4 DNA Ligase buffer optimizes ligation, which can be performed in 5 minutes (1). Single-stranded nucleic acids are not substrates for this enzyme. A T4 DNA Ligase Technical Bulletin is available.
Applications: Cloning (blunt-end or cohesive-end ligation) (2). Adding linkers or adapters to blunt-ended DNA (2).
Source: Purified from E. coli œ lysogen NM989.
Performance and Quality Testing: Endodeoxyribonuclease, 3´ and 5´ exodeoxyribonuclease assays; ligation efficiency tested.
Unit Definition: One unit catalyzes the exchange of 1 nmol 32P-labeled pyrophosphate into ATP in 20 min. at 37°C. (One unit is equal to approximately 300 cohesive-end ligation units.)
Unit Reaction Conditions: 66 mM Tris-HCl (pH 7.6), 6.6 mM MgCl2 , 10 mM DTT, 66 µM ATP, 3.3 µM 32 P-labeled pyrophosphate, and enzyme in 0.1 ml for 20 min. at 37°C.