The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The Gateway™ pcDNA™-DEST40 vector자세히 알아보기
Have Questions?
카탈로그 번호
수량
12274015
12274-015으로도 사용됨
6 μg
카탈로그 번호 12274015
12274-015으로도 사용됨
제품 가격(KRW)
1,102,000
Each
카트에 추가하기
수량:
6 μg
제품 가격(KRW)
1,102,000
Each
카트에 추가하기
The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The Gateway™ pcDNA™-DEST40 vector offers the following key features:
•C-terminal V5-6x His tag for easy detection and rapid purification •Cytomegalovirus (CMV) promoter for high-level expression •attR sites for Gateway™ cloning, enabling recombination with attL-flanked fragments •Neomycin resistance gene for stable selection •Ampicillin resistance gene and pUC origin for selection and maintenance in E. coli
Gateway™ Cloning To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins. All Gateway™ destination vectors have attR sites for recombination with any attL-flanked fragment, regardless of whether it is an entry clone or an Ultimate™ ORF Clone. The following table lists a variety of available destination vectors.
Additional materials required, available separately: Gateway™ entry clone, appropriate Gateway™ LR Clonase™ enzyme mix, and reaction buffer.
For Research Use Only. Not for use in diagnostic procedures.
사양
구성 또는 유도성 시스템Constitutive
배달 유형Transfection
용도(애플리케이션)Constitutive Expression
제품 유형Gateway System Destination Expression Vector
수량6 μg
선택 제제(진핵)Geneticin™ (G-418)
벡터pDEST
클로닝 방법Gateway
제품라인Gateway, pDEST
프로모터CMV
단백질 태그His Tag (6x), V5 Epitope Tag
Unit SizeEach
구성 및 보관
All destination vectors are provided lyophilized and supercoiled.
자주 묻는 질문(FAQ)
Can I perform the single-step protocol for the BP/LR Clonase reaction using BP Clonase enzyme and LR Clonase enzyme instead of BP Clonase II enzyme and LR Clonase II enzyme?
In the single-step protocol for the BP/LR Clonase reaction, we would not recommend substituting the BP Clonase II/LR Clonase II enzymes with BP Clonase /LR Clonase enzymes as this would result in very low recombination efficiency.
Do you have a recommended single-step protocol for BP/LR recombination?
Yes, we have come up with a single-step protocol for BP/LR Clonase reaction (http://www.thermofisher.com/us/en/home/life-science/cloning/gateway-cloning.html#1), where DNA fragments can be cloned into Destination vectors in a single step reaction, allowing you to save time and money.
How can I move my gene of interest from a Gateway-adapted expression clone to a new Destination vector as I have lost the entry clone?
We would recommend performing a BP reaction with a Donor vector in order to obtain an entry clone. This entry clone can then be used in an LR reaction with the Destination vector to obtain the new expression clone.
Can I purchase the 5X LR Clonase buffer or 5X BP Clonase buffer separately?
We do not offer the 5X LR Clonase buffer and 5X BP Clonase buffer as standalone products. They are available as part of the enzyme kits.
Do you offer Gateway vectors for expression in plants?
We do not offer any Gateway vectors for expression in plants.
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Authors:Sugimoto M,Fujikawa A,Womack JE,Sugimoto Y
Journal:Proceedings of the National Academy of Sciences of the United States of America
PubMed ID:16611727
Mastitis, a mammary gland inflammation in response to bacterial infection, is a major problem in the dairy industry. We found that cows susceptible to mastitis have a three-base insertion in a glycine-coding stretch of the gene for forebrain embryonic zinc finger-like (FEZL), a transcription factor with a role in neuronal ... More
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PubMed ID:14645524
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