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8 results for "USLP102219LP00041"

8 Results for: "USLP102219LP00041"

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Vector, pUC 18, MP Biomedicals

Supplier: MP Biomedicals

pUC 18 is a small vector of approximately 2.7 Kb containing the Pvu II/EcoR I fragment of pBR322 and the lacZ gene multiple cloning site from M13mp18.

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Novagen® pET-28b(+) DNA, MilliporeSigma

Supplier: MilliporeSigma

The pET-28a-c(+) vectors carry an N-terminal His Tag®/thrombin/T7 Tag® configuration plus an optional C-terminal His Tag sequence.

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Novagen® pET-21a Vectors, MilliporeSigma

Supplier: MilliporeSigma

The pET-21a vectors carry an N-terminal T7 Tag® sequence plus an optional C-terminal His Tag® sequence.

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Novagen® pET-23a-d(+) Vectors, MilliporeSigma

Supplier: MilliporeSigma

The pET-23a-d(+) vectors carry an N-terminal T7 Tag® sequence plus an optional C-terminal His Tag® sequence.

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AdEasy Adenoviral Vector Systems, Agilent Technologies

AdEasy Adenoviral Vector Systems, Agilent Technologies

Supplier: Agilent Technologies

The AAV helper-free system eliminates the requirement for wild-type adenovirus co-infection from both AAV vector production and AAV stock titering steps, making this system entirely helper virus-free and safer.

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pETDuet™-1 DNA Bacterial Expression Vector, EMD MilliporeSigma

Supplier: MilliporeSigma

pETDuet-1 is designed for the coexpression of two target genes. The vector encodes two multiple cloning sites (MCS), each of which is preceded by a T7 promoter, lac operator and ribosome binding sites.

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AdEasy Adenoviral Vector Systems, Agilent Technologies

AdEasy Adenoviral Vector Systems, Agilent Technologies

Supplier: Agilent Technologies

The AdEasy system saves you a month of work over traditional methods by producing the recombinant adenoviral plasmid by homologous recombination in E. coli. The AdEasy XL system includes BJ5183 cells pre-transformed with the pAdEasy-1 plasmid, this feature dramatically decreases background caused by the non-recombinant shuttle plasmid.

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Expression vectors, pGEX

Expression vectors, pGEX

Supplier: Cytiva

The pGEX vectors have an expanded multiple cloning site (MCS) that contains six restriction sites. The expanded MCS facilitates the unidirectional cloning of cDNA inserts obtained from libraries constructed using many available lambda vectors. pGEX-6P-1, pGEX-6P-2, and pGEX-6P-3 each encode the recognition sequence for site-specific cleavage by PreScission Protease between the GST domain and the multiple cloning site. pGEX-4T-1, pGEX-4T-2, and pGEX-4T-3 are derived from pGEX-2T and contain a Thrombin recognition site. pGEX-5X-1, pGEX-5X-2, and pGEX5X-3 are derivatives of pGEX-3X and possess a Factor Xa recognition site.

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