The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The pcDNA6.2/V5-pL-DEST vector offers자세히 알아보기
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카탈로그 번호
수량
12537162
12537-162으로도 사용됨
6 μg
카탈로그 번호 12537162
12537-162으로도 사용됨
제품 가격(KRW)
758,000
Online offer
Ends: 31-Mar-2026
891,000
할인액 133,000 (15%)
Each
수량:
6 μg
제품 가격(KRW)
758,000
Online offer
Ends: 31-Mar-2026
891,000
할인액 133,000 (15%)
Each
The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The pcDNA6.2/V5-pL-DEST vector offers the following key features:
•Promoterless version of the pcDNA™6.2⁄V5-DEST vector (cat. no. 12489027) •attR sites for Gateway™ cloning •Compatible with MultiSite Gateway™ Pro kits (e.g. cat. no. 12537100) •C-terminal V5 tag for easy detection •Blasticidin resistance gene for efficient 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
배달 유형Transfection
발현 시스템Mammalian
용도(애플리케이션)Clone your own Promoter, Multi-Gene Expression
용도(장비)MultiSite Gateway™ Pro kits (e.g. cat. no. 12537-100)
제품 유형Mammalian Expression Vector
단백질 태그 위치(유전자에 대해)C-terminal
수량6 μg
벡터pcDNA, pDEST, MultiSite Gateway Vectors
클로닝 방법Gateway
제품라인Gateway, pcDNA
프로모터None (Promoterless)
단백질 태그V5 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.