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CRISPRi Libraries, Pools, and gRNAs

Merck

Nuclease-independent applications of CRISPR provide equal targeting specificity but instead of cutting, CRISPRi allows for targeted interference of gene function by delivering transcriptional repressor domains to a specific target sequence using modified dCas9 + gRNA complexes. Gene knockdown is complementary to CRISPR-KO and CRISPRa (activation) and has distinct advantages over existing loss-of-function strategies like RNAi.…

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NutriStem® hPSC XF Media

Sartorius Group

Xeno-free, serum-free stem cell culture media designed to support the growth and expansion of undifferentiated human embryonic stem cells (hESC), and human induced pluripotent stem cells (hiPSC).  

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InterPlay Adenoviral C-Terminal TAP System

Agilent Technologies

The InterPlay adenoviral TAP System combines our unique tandem affinity purification (TAP) system with our exclusive adenoviral gene delivery system, the AdEasy Adenoviral Vector System for enhanced gene delivery to a broader range of mammalian cells, higher protein yields, and improved purification and analysis of endogenous interacting protein partners.

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InterPlay Adenoviral N-Terminal TAP System

Agilent Technologies

The InterPlay adenoviral TAP System combines our unique tandem affinity purification (TAP) system with our exclusive adenoviral gene delivery system, the AdEasy Adenoviral Vector System for enhanced gene delivery to a broader range of mammalian cells, higher protein yields, and improved purification and analysis of endogenous interacting protein partners.

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ECACC

Merck

Authenticated, validated, quality-controlled mammalian cell lines offered in partnership with the European Collection of Authenticated Cell Cultures (ECACC) repository.

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