Product Image
Invitrogen™

pTrcHis2 TOPO™ TA 表达试剂盒

pTrcHis- 和 pTrcHis2-TOPO™ TA 表达试剂盒能够快速、高效地将 PCR 产物克隆到原核表达载体中,从而从 trc 启动子获得高水平了解更多信息
Have Questions?
货号数量
K44000120 reactions
货号 K440001
价格(CNY)
15,581.00
Each
数量:
20 reactions
价格(CNY)
15,581.00
Each
pTrcHis- 和 pTrcHis2-TOPO™ TA 表达试剂盒能够快速、高效地将 PCR 产物克隆到原核表达载体中,从而从 trc 启动子获得高水平、可控的表达。各试剂盒中的载体,pTrcHis-TOPO™ 或 pTrcHis2-TOPO™,包括用于提高大肠杆菌中真核蛋白的翻译效率的迷你顺反子元素。两种载体均提供线性化且经拓扑异构酶 I 活化 5 分钟的 TOPO™ 克隆,克隆效率可达 >85%。为简化蛋白纯化和检测,pTrcHis-TOPO™ 和 pTrcHis2-TOPO™ 载体包括以下特点:

pTrcHis-TOPO™

N 端 Xpress™ 抗原决定簇,可采用抗 Xpress™ 抗体进行检测
• N 端多聚组氨酸 (6xHis) 标签,可采用镍螯合树脂进行纯化并采用抗 HisG 抗体进行检测
•肠激酶切割位点,可高效去除 N 端融合标签

pTrcHis2-TOPO™
C 端 c-myc 抗原决定簇,可采用抗 myc 抗体进行检测
• C 端多聚组氨酸 (6xHis) 标签,可采用镍螯合树脂进行纯化并采用抗 His(C 端)抗体进行检测
仅供科研使用。不可用于诊断程序。
规格
耐抗生素细菌氨苄青霉素 (AmpR)
细菌或酵母菌株TOP10
切割EK(肠激酶)识别位点
构成或诱导系统诱导
表达机制基于细胞的表达
表达系统大肠杆菌
诱导剂IPTG:
产品类型TA 表达试剂盒
数量20 reactions
选择试剂(真核生物)
载体pTrc
克隆方法TOPO™-TA
产品线TOPO
促进剂Trc, lacO
蛋白标记His 标签 (6x)、c-Myc 抗原决定簇标签, c-Myc Epitope Tag
Unit SizeEach
内容与储存
pTrcHis- 和 pTrcHis2-TOPO™ TA 表达试剂盒各包含两个盒。TOPO™ TA 盒包含 200 ng 线性化、拓扑异构酶 I 活化 pTrcHis-TOPO™ 或 pTrcHis2-TOPO™ 载体;无菌水;dNTP;10X PCR 缓冲液;对照模板和引物;测序或 PCR 筛选用引物以及表达对照质粒。One Shot™ TOP10 盒中含有 21 份 50 µL 化学感受态 TOP10 大肠杆菌、S.O.C. 培养基和超螺旋对照质粒等份试液。TOPO TA Cloning™ 盒储存于 -20°C 下。One Shot™ 盒储存于 -80°C 下。正确存放时,所有试剂均可保证 6 个月的稳定。

常见问题解答 (FAQ)

我可将感受态细胞存储在液氮中吗?

我们不建议将感受态细胞保存在液氮中,因为极端温度会损害细胞。另外,装感受态细胞的塑料管子可能承受不了如此低的温度,从而发生破裂。

我应该如何存储我的感受态E. Coli?

我们推荐将感受态细胞存储在-80摄氏度。高于这个温度,即使存储时间很短,也会显著降低其转化效率。

pTrc系统表达使用TOP10、DH5α或其他克隆菌株和使用BL21 Star(DE3)或BL21(DE3)细胞相比的优点和/或缺点是什么?

TOP10、DH5α、其他克隆菌株
优点:
- 省时,可直接从克隆到表达。
-甘油储液更稳定,因为这些菌株的基因型是endA-和recA-。
缺点:
-如果目的基因具有毒性,则克隆步骤会变得困难。
-这些克隆菌株不是蛋白酶缺陷型的;因此,蛋白质可能被降解。

BL21 Sta(DE3)或BL21(DE3)
优点:
-这些表达菌株是蛋白酶缺陷型的。
缺点:
-您需要将质粒转化到表达菌株中。
-甘油储液可能不稳定,因为这些表达菌株的基因型不是endA-和recA-。
-(DE3)部分是多余的,因为启动子不需要T7 RNA聚合酶。

哪种感受态细胞可用于pTrc表达系统的表达?

pTrc启动子可被大肠杆菌RNA聚合酶识别,而不是T7聚合酶,因此,pTrc启动子可在任何大肠杆菌菌株中表达,而不仅仅是BL21菌株。所以,您可使用Top10、DH5α等进行表达。但是,如果您的目的基因具有毒性,则会因表达渗漏而出现克隆困难。

葡萄糖如何抑制pTrc启动子?

一种被称为CAP(代谢产物活化蛋白)的转录激活蛋白,通常可结合到trc启动子的上游并激活转录。该蛋白需要cAMP才能与DNA结合。在培养基中加入葡萄糖可降低细胞内cAMP水平。在LB培养基和琼脂板中补充葡萄糖,会抑制trc启动子的基础水平转录。为确保插入片段的稳定性,我们建议您在选择培养基中加入25 mM或0.5%葡萄糖。

引用和文献 (5)

引用和文献
Abstract
Characterization of a Novel Drosophila melanogaster Galectin. EXPRESSION IN DEVELOPING IMMUNE, NEURAL, AND MUSCLE TISSUES.
Authors: Pace Karen E; Lebestky Tim; Hummel Thomas; Arnoux Pascal; Kwan Kent; Baum Linda G;
Journal:J Biol Chem
PubMed ID:11809773
'We have cloned and characterized the first galectin to be identified in Drosophila melanogaster. The amino acid sequence of Drosophila galectin showed striking sequence similarity to invertebrate and vertebrate galectins and contained amino acids that are crucial for binding beta-galactoside sugars. Confirming its identity as a galectin family member, the ... More
Kaposi's Sarcoma-Associated Herpesvirus/Human Herpesvirus 8 Transcriptional Activator Rta Is an Oligomeric DNA-Binding Protein That Interacts with Tandem Arrays of Phased A/T-Trinucleotide Motifs.
Authors:Liao W, Tang Y, Kuo YL, Liu BY, Xu CJ, Giam CZ,
Journal:J Virol
PubMed ID:12915555
'Kaposi''s sarcoma associated herpesvirus (KSHV)/human herpesvirus 8 (HHV-8) encodes an immediate early transcriptional activator, Rta, which mediates viral reactivation from latency and lytic viral replication. Here we report the purification and characterizations of HHV-8 Rta and its interaction with Rta-responsive DNA elements. The Rta response element (RtaRE) in the promoter ... More
Assimilation of nicotinamide mononucleotide requires periplasmic AphA phosphatase in Salmonella enterica.
Authors:Grose JH, Bergthorsson U, Xu Y, Sterneckert J, Khodaverdian B, Roth JR,
Journal:J Bacteriol
PubMed ID:15968063
'Salmonella enterica can obtain pyridine from exogenous nicotinamide mononucleotide (NMN) by three routes. In route 1, nicotinamide is removed from NMN in the periplasm and enters the cell as the free base. In route 2, described here, phosphate is removed from NMN in the periplasm by acid phosphatase (AphA), and ... More
Transition state analogue inhibitors of purine nucleoside phosphorylase from Plasmodium falciparum.
Authors: Kicska Gregory A; Tyler Peter C; Evans Gary B; Furneaux Richard H; Kim Kami; Schramm Vern L;
Journal:J Biol Chem
PubMed ID:11707439
'Immucillins are logically designed transition-state analogue inhibitors of mammalian purine nucleoside phosphorylase (PNP) that induce purine-less death of Plasmodium falciparum in cultured erythrocytes (Kicska, G. A., Tyler, P. C., Evans, G. B., Furneaux, R. H., Schramm, V. L., and Kim, K. (2002) J. Biol. Chem. 277, 3226-3231). PNP is present ... More
Characterization of monomeric L1 metallo-beta -lactamase and the role of the N-terminal extension in negative cooperativity and antibiotic hydrolysis.
Authors: Simm Alan M; Higgins Catherine S; Carenbauer Anne L; Crowder Michael W; Bateson John H; Bennett Peter M; Clarke Anthony R; Halford Stephen E; Walsh Timothy R;
Journal:J Biol Chem
PubMed ID:11940588
The L1 metallo-beta-lactamase from Stenotrophomonas maltophilia is unique among this class of enzymes because it is tetrameric. Previous work predicted that the two regions of important intersubunit interaction were the residue Met-140 and the N-terminal extensions of each subunit. The N-terminal extension was also implicated in beta-lactam binding. Mutation of ... More