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T4 DNA连接酶
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价格:¥电议
更新日期:2026/8/7 18:54:55
生 产 地:中国大陆
产品型号:9015-85-4
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详细内容
T4 DNA连接酶T4 DNA连接酶/T4 DNA LigaseBR,1u/ulLC1000u,Sigma-Aldrich、Amresco、Amersham、Serva、AppliChem等品牌,9015-85-4保存:-20℃
BR,5u/ul200u,Sigma-Aldrich、Amresco、Amersham、Serva、AppliChem等品牌,
中文名称:T4 DNA连接酶
英文名称: T4 DNA Ligase
产品规格: BR,1u/ul
包装: LC1000U
产品规格: BR,5u/ul
包装: 200U/1000U
产品规格: BR,30u/ul
包装: HC5000U
CAS号:9015-85-4
分子量:55.3kDa,单体
级别:BR
分子量:55.3kDa,单体
来源:含有T4克隆基因30的
浓度:1u/ul(200CEU/ul)
浓度:5Weiss u/ul(1000CEU/ul)
浓度:30Weiss u/ul(6000CEU/ul)
活性定义:是指在ATP-PPi交换反应中,37℃、30分钟内将1nmol [32PPi]转换为Norit可吸收形式所需的酶量(weiss单位,1个weiss单位相当于约200个粘性末端连接单位。1个粘性末端连接单位:20ul反应体系(50mM Tris-HCL(PH7.5), 10mM DTT, 10mM MgCL2, 1mM ATP, 25ug/ml BSA, 12uM(300ug/ml)的5-DNA末端)中,在16℃、30分钟内连接50%连接HindIII酶切的Lambda DNA 产物所需的酶量)
酶活性分析混合物:66mM Tris-HCL(PH7.6), 10mM DTT, 6.6mM MgCL2, 0.066mM ATP, 3.3uM[32PPi]
保存液组分:20mM Tris-HCL(PH7.5), 50mM KC1, 1mM DTT,0.1mM EDTA和50%(v/v)甘油
10×T4 DNA Ligase缓冲液(#B69):400mM Tris-HCL, 100mM MgCL2, 100mM DTT, 5mM ATP(PH7.5,25℃)
抑制剂:当反应体系中NaC1或KC1的浓度超过200 mM时,可强烈抑制T4 DNA Ligase活性
失活:65℃加热10分钟或70℃加热5分钟
注意:T4 DNA Ligase与DNA结合会改变条带的琼脂糖凝胶电泳迁移率,为避免此现象,电泳前需处理样本或分子量标准。样本处理如下:样本与Fermentas公司6×DNA Loading Dye&SDS溶液(#R1151)混合,75℃加热5分钟或65℃加热10分钟后冰浴保存;转化时,连接产物的体积不得超过感受态细胞体积中的10%;电转化之前,先用抽提方法除去连接混合物中的T4 DNA Ligase,然后经乙醇沉淀纯化抽提产物
质量控制:测试表明无内切脱氧核糖核酸酶、核糖核酸酶、磷酸酶污染。功能检测:粘性末端或平末端DNA的连接能力
性状:液体。该酶催化双链DNA或RNA中毗邻的5'磷酸基团和3'-羟基末端之间形成磷酸二酯键,还可以修复双链DNA、RNA或DNA/RNA复合体中的单链切口,连接DNA的粘性和平末端,但该酶对单链核酸无酶活性。该酶需要辅因子ATP
用途:生化研究。粘性末端或平末端双链DNA的连接;双链寡核苷酸接头与双链DNA连接;双链DNA、RNA或DNA-RNA复合体中缺口的修复;连接酶介导的RNA检测;位点特异性突变;扩增片段长度多态性
保存: -20°C
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公司代理AMRESCO、Sigma、Aldrich、Fluka/RdH、Supelco、TCI等品牌试剂,以化学试剂经营优势满足实验室、研究室、化验室专业客户群需求。用专业解决问题;用诚信提供服务;用质量树立品牌。同时,与众多化学品和实验室产品的生产商和经销商结成长期、稳定、广泛的战略合作关系。
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