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pINA1292 BioVector®解脂耶氏酵母表达质粒 / pINA1292 Plasmid BioVector NTCC典型培养物保藏中心

  • 价  格:¥99850
  • 货  号:BioVector® pINA1292
  • 产  地:北京
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BioVector® pINA1292解脂耶氏酵母表达质粒 / pINA1292 Plasmid 数据说明书

产品名称: BioVector® pINA1292 质粒
中文名称: BioVector® pINA1292 解脂耶氏酵母表达质粒(多拷贝整合型)
英文名称: BioVector® pINA1292 Yarrowia lipolytica Expression Plasmid (Multicopy Integrative Vector)
产品类别: 酵母表达载体
质粒类型: 穿梭质粒;多拷贝整合型解脂耶氏酵母表达载体
用途: 在解脂耶氏酵母中实现外源基因的多拷贝整合与高效表达;蛋白生产;代谢工程研究;基因功能研究 -2-7
来源信息: 由法国农业科学研究院构建并保藏 -4
载体大小: 相关信息缺失
复制子: pBR322 ori(在大肠杆菌中复制)-4
启动子: hp4d 启动子(组成型杂交启动子,来源于LEU2启动子和XPR2启动子的UAS1区)-4
终止子: XPR2 终止子 (XPR2t) -4
筛选标记:

  • 大肠杆菌筛选:相关信息缺失

  • 酵母筛选:URA3 营养缺陷型标记(携带ura3d4缺陷型等位基因,可实现多拷贝整合)-4-7
    信号肽: 无信号肽(用于胞内表达)-4
    多克隆位点: 上游酶切位点:PmlI (平末端);下游酶切位点:BamHI, KpnI -4
    特性特征:

  1. 宿主范围: 可在大肠杆菌中扩增,在解脂耶氏酵母中整合表达

  2. 整合特性: 属于“自动克隆”载体系列,表达盒可通过NotI酶切释放,去除细菌序列后转化酵母;携带ura3d4缺陷型标记,可在解脂耶氏酵母中实现多拷贝整合 -4-7

  3. 表达特性: hp4d启动子为组成型启动子,无需诱导即可驱动外源基因表达

  4. 应用: 广泛用于解脂耶氏酵母中外源蛋白的高水平表达、代谢途径工程、工业酶生产等研究。该载体已成功用于过表达delta-12去饱和酶以生产亚油酸,并研究其细胞毒性效应 -2-7
    相关质粒: BioVector® pINA1312(单拷贝整合版本,携带ura3d1等位基因);BioVector® pINA1293(携带LIP2信号肽的分泌表达版本)-4
    质控载体: BioVector® pUC19 质粒
    宿主菌: BioVector® DH5α 化学感受态细胞
    质量控制: 测序验证:100%正确;无菌检测:阴性;酶切鉴定:符合预期条带
    储存与运输: -20°C或干冰运输与保存
    仅供科研使用


English:
BioVector® pINA1292 Plasmid Datasheet

Product Name: BioVector® pINA1292 Plasmid
Chinese Name: BioVector® pINA1292 解脂耶氏酵母表达质粒(多拷贝整合型)
English Name: BioVector® pINA1292 Yarrowia lipolytica Expression Plasmid (Multicopy Integrative Vector)
Product Category: Yeast Expression Vector
Plasmid Type: Shuttle Plasmid; Multicopy Integrative Yarrowia lipolytica Expression Vector
Purpose: Multicopy integration and high-level expression of foreign genes in Yarrowia lipolytica; protein production; metabolic engineering research; gene function studies -2-7
Source: Constructed and deposited by the French National Institute for Agricultural Research -4
Vector Size: Information missing
Replicon: pBR322 ori (for propagation in E. coli) -4
Promoter: hp4d promoter (constitutive hybrid promoter derived from the LEU2 promoter and the UAS1 region of the XPR2 promoter) -4
Terminator: XPR2 terminator (XPR2t) -4
Selection Markers:

  • E. coli Selection: Information missing

  • Yeast Selection: URA3 auxotrophic marker (carries the ura3d4 defective allele for multicopy integration) -4-7
    Signal Peptide: None (for intracellular expression) -4
    Multiple Cloning Site: Upstream site: PmlI (blunt end); Downstream sites: BamHI, KpnI -4
    Characteristics:

  1. Host Range: Can be amplified in E. coli and integrated for expression in Yarrowia lipolytica

  2. Integration Properties: Belongs to the "auto-cloning" vector series; the expression cassette can be released by NotI digestion to remove bacterial sequences before transformation; carries the ura3d4 defective marker enabling multicopy integration in Yarrowia lipolytica -4-7

  3. Expression Characteristics: The hp4d promoter is constitutive, driving foreign gene expression without induction

  4. Applications: Widely used for high-level expression of foreign proteins in Yarrowia lipolytica, metabolic pathway engineering, industrial enzyme production research. This vector has been successfully used to overexpress delta-12 desaturase for linoleic acid production and to study its cytotoxic effects -2-7
    Related Plasmids: BioVector® pINA1312 (single-copy integration version carrying ura3d1 allele); BioVector® pINA1293 (secretory expression version with LIP2 signal peptide) -4
    Control Vector: BioVector® pUC19 Plasmid
    Host Strain: BioVector® DH5α Chemically Competent Cells
    Quality Control: Sequencing Validation: 100% correct; Sterility: Negative; Restriction Digestion: Expected bands
    Storage and Shipment: Stored and shipped at -20°C or on dry ice
    For Research Use Only


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