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pcDNA6/V5-His A

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产品名称: pcDNA6/V5-His A
产品型号:
产品展商: HZbscience
产品文档: 无相关文档

简单介绍

pcDNA6/V5-His A的各批次质粒菌株发货前均经过严格的多重验证,如存在质量问题,请在收到产品的三个月内通知我司。收到pcDNA6/V5-His A后请短暂离心,取2μl转化至对应感受态中,挑取单克隆重新提取质粒后使用。


pcDNA6/V5-His A  的详细介绍

pcDNA6/V5-His A载体基本信息

载体名称: pcDNA6/V5-His A
质粒类型: 哺乳动物表达载体;cDNA表达载体
高拷贝/低拷贝: 高拷贝
克隆方法: 限制性内切酶,多克隆位点
启动子: CMV
载体大小: 5144 bp
5' 测序引物及序列: T7 Forward: 5’-TAATACGACTCACTATAGGG-3’
3' 测序引物及序列: BGH Reverse: 5’-TAGAAGGCACAGTCGAGG-3’
载体标签: V5 Epitope(C-端);His tag(C-端)
载体抗性: 氨苄青霉素
筛选标记: Blasticidin
克隆菌株: TOP10F´, JM109 and INVaF´
宿主细胞(系): 常规细胞系,如293、Hela等
备注: pcDNA6/V5-His A载体是cDNA的表达与克隆载体;
CMV启动子驱动目的基因的过表达;
易于克隆到其它载体中去;
pcDNA6/V5-His A,B,C仅阅读框不同。
产品目录号: V220-01
稳定性: 瞬表达 或 稳表达
组成型/诱导型: 组成型
病毒/非病毒: 非病毒

pcDNA6/V5-His A载体质粒图谱和多克隆位点信息

pcDNA6-V5-His A载体图谱



pcDNA6-V5-His A 多克隆位点

pcDNA6-V5-His 载体特征1
pcDNA6-V5-His 载体特征2

pcDNA6/V5-His A载体简介

pcDNA6/V5-His A, B, and C are 5.1 kb vectors derived from pcDNA3.1(+) and designed for high-level expression, selection on blasticidin, purification, and detection of recombinant proteins in mammalian hosts. High-level stable and non-replicative transient expression can be carried out in most mammalian cells. pcDNA6/V5-His A, B, and C 含有以下元件: • Human cytomegalovirus immediate-early (CMV) promoter for high-level expression in a wide range of mammalian cells
• Three reading frames to facilitate in-frame cloning with a C-terminal tag encoding the V5 epitope and a polyhistidine metal-binding peptide
• Blasticidin resistance gene (BSD) from Aspergillus terreus for selection in prokaryotic and eukaryotic cells (Kimura et al., 1994)
• Episomal replication in cell lines that are latently infected with SV40 or that express the SV40 large T antigen (e.g. COS7)
The control plasmid, pcDNA6/V5-His/lacZ, is the pcDNA6/V5-His A vector with a 3.2 kb fragment containing the β-galactosidase gene cloned in frame with the C-terminal peptide (see page 11). It is included for use as a positive control for transfection, expression, purification, and detection in the cell line of choice. 实验流程 使用pcDNA.6/V5-His 载体表达目的基因的实验流程: 1. Consult the multiple cloning sites described on pages 3–5 to determine which vector (A, B, or C) should be used to clone your gene in frame with the C-terminal V5 epitope and polyhistidine tag.
2. Ligate your insert into the appropriate vector and transform into E. coli. Select transformants on 100 μg/mL blasticidin or 50 to 100 μg/mL ampicillin.
3. Analyze your transformants for the presence of insert by restriction digestion.
4. Select a transformant with the correct restriction pattern and confirm that your gene is in frame with the C-terminal peptide by sequencing.
5. Transfect your construct into the cell line of choice using your own method of transfection.
6. Test for expression of your recombinant gene by western blot analysis or functional assay. If you do not have an antibody to your protein, Life Technologies offers the Anti-V5 Antibody or the Anti-His(C-term) Antibody to detect your recombinant fusion protein.
7. To purify your recombinant fusion protein, you may use metal-chelating resin such as ProBond.. ProBond. resin is available separately. 

pcDNA6/V5-His A载体序列

hz-8629R phospho-Na+/K+-ATPase Alpha1(Ser 943)  磷酸化钠钾ATP酶α1多肽抗体
hz-8634R FOXA1/HNF3-alpha  转录因子HNF-3α抗体
hz-8650R T2R38/TAS2R38  味觉感受器蛋白T2R38抗体
hz-4156R PRKD1/PKC mu  蛋白激酶C mu型抗体
hz-8654R FAM81A  FAM81A蛋白抗体
hz-5561R phospho-PRKD1(Ser738)  磷酸化蛋白激酶C mu型抗体
hz-8660R Salmonella typhimurium O  伤寒沙门氏菌体蛋白O抗原抗体
hz-8662R BASP1/Nap22  脑富含膜附着信号蛋白1抗体
hz-8670R Salmonella enteritidis H  伤寒沙门氏菌鞭毛抗原H抗体
hz-5562R phospho-PRKD1(Ser742)  磷酸化蛋白激酶C mu型抗体
hz-8671R MMS19  DNA修复甲基磺酸敏感性基因19抗体
hz-8672R HDL/high density lipoprotein  高密度脂蛋白抗体
hz-8673R KCTD12  钾离子通道多聚体结构域蛋白12抗体
hz-8675R BDKRB1  缓激肽B1受体抗体
hz-5563R phospho-PRKD1(Tyr463)  磷酸化蛋白激酶C mu型抗体
hz-8683R IGF2BP1/IMP1  胰岛素样生长因子ⅡmRNA结合蛋白1抗体
hz-8686R BRMS1  乳腺癌转移抑制基因1抗体
hz-8687R p53 (FL-393)  肿瘤抑制基因p53抗体
hz-8689R MEPE  细胞外基质磷酸化抗体

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