rna-isolation-purification-tissue-mouse-small-intestine

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Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Mouse - ESCs (Embryonic Stem Cells)

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using Ovation® RNA Amplification System V2 to perform Microarray RNA amplification & Labeling - Mouse cochlaea Biotin

Products NuGEN Ovation® RNA Amplification System V2

Get tips on using Enzo BioArray™ Single-Round RNA Amplification and Biotin Labeling System to perform Microarray Rhesus monkey - Brain tissue Target preparation (RNA amplification + labeling)

Products Enzo Life Sciences Enzo BioArray™ Single-Round RNA Amplification and Biotin Labeling System

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

Products R&D Systems Mouse Prolactin DuoSet ELISA

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

Products R&D Systems Mouse Myeloperoxidase DuoSet ELISA

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

Products Sigma-Aldrich Mouse Leptin ELISA Kit

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

Products Sigma-Aldrich Mouse Decorin ELISA Kit

Get tips on using RNeasy Mini Kit to perform RNA isolation / purification Cells - Cancer cell lines Liver cancer cell lines Hepato cellular carcenoma (SMMC-7721, Huh7 & HepG2))

Products Qiagen RNeasy Mini Kit

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

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 Repression Mstn

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