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Transfer SKU PMIR-REPORT REPORTER VECTOR 0.5ML,AM5795,赛默飞世尔

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订货号 5MT0317
品牌型号 赛默飞世尔 AM5795
货期 询货期
最小订货量 1套
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产品介绍 Product Description
规格
Cloning Method: Restriction Enzyme ⁄ MCS
Constitutive or Inducible System: Constitutive
Delivery Type: Transfection
Product Line: Ambion™, pMIR-REPORT™
Promoter: CMV
RNAi Type: miRNA
Reporter Gene: Beta-Gal (lacZ), Luciferase
Selection Agent (Eukaryotic): Puromycin
Selection Marker Promoter: SV40 Promoter
Shipping Condition: Dry Ice
Vector: pMIR
储存
pMIR-REPORT™ Luciferase and pMIR-REPORT™ β-gal Control Plasmid are both supplied as glycerol stocks in E. coli and should be stored at –70°C.
描述

The Ambion® pMIR-REPORT™ miRNA Expression Reporter Vector System is for the measurement of miRNA expression in cells. It contains two mammalian expression vectors—one for cloning miRNA targets and evaluating miRNA regulation, and the other for the normalization of transfection efficiency.

• Clone miRNA targets and evaluate miRNA regulation
• Screen putative miRNA target sequences
• Includes both reporter and control vectors

The pMIR-REPORT™ miRNA Expression Reporter Vector System provides accurate, quantitative, in-cell measurement of miRNA expression. This validated reporter system contains two mammalian expression vectors. The pMIR-REPORT™ Luciferase miRNA Expression Reporter Vector contains firefly luciferase under the control of a mammalian promoter/terminator system, with an miRNA target cloning region downstream of the luciferase translation sequence. This vector is optimized for cloning miRNA targets and evaluating miRNA regulation. A second vector, pMIR-REPORT™ Beta-galactosidase Reporter Control Vector, is provided for normalizing transfection efficiency.

Applications:
pMIR-REPORT™ Luciferase is designed for cloning and testing putative miRNA binding sites. pMIR-REPORT™ Luciferase can be transfected into mammalian cells to evaluate endogenous miRNA expression, or used to evaluate the up- or down-regulation resulting from the transfection of Pre-miR™ miRNA Molecules or Anti-miR™ miRNA Inhibitor Molecules, respectively.

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