siRNA / miRNA gene silencing Mouse Colon26

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Get tips on using Mouse/Rat TrkC Antibody to perform Immunohistochemistry Mouse - TrkC

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Get tips on using Mouse Prolactin DuoSet ELISA to perform ELISA Mouse - PRL

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Get tips on using Mouse Myeloperoxidase DuoSet ELISA to perform ELISA Mouse - MPO

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Get tips on using Mouse Leptin ELISA Kit to perform ELISA Mouse - Leptin

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Get tips on using Mouse Decorin ELISA Kit to perform ELISA Mouse - Decorin

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Reporter gene assays enable high sensitivity measurement of gene expression and cell signaling through the addition of bioluminescent genes into target cells. One of the major challenges is to make a specific construct that has no responses other than those related to the signaling pathway of interest. This can be achieved by selecting highly specific reporter constructs containing only defined responsive elements and a minimal promoter linked to reporter enzymes such as luciferase

Cellular assays Reporter gene assay luciferase SW480 human colon cancer cell line

Get tips on using Mouse Osteopontin/OPN Antibody to perform Immunohistochemistry Mouse - Spp1/OPN

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Get tips on using TLR10 shRNA (h) Lentiviral Particles to perform shRNA gene silencing Human - THP-1 TLR10

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Get tips on using TLR10 shRNA (h) Lentiviral Particles to perform shRNA gene silencing Human - THP-1 TLR10

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The RNA-guided CRISPR-Cas9 nuclease system has revolutionized the genome editing practices. For the most part, the Cas9-mediated genome editing is performed either via nonhomologous end joining (NHEJ) or homology-directed repair (HDR) in mammalian cells, However, designing of specific sgRNAs and minimizing off-target cleavage mediated mutagenesis are the major challenges in CRISPR-Cas based genome editing. To circumvent these issues, we can take advantages of many available tools and approaches for sgRNA construction and delivery.

DNA CRISPR Mouse Deletion Dck

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