DNA Damage Assay Human bronchial epithelial cells (hBE)

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Get tips on using Anti-Notch1 antibody (ab27526) to perform Immunohistochemistry Human - Notch1

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Get tips on using MLH1 antibody [G168-15] to perform Immunohistochemistry Human - MLH1

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Get tips on using Anti-CRISP3 antibody (ab105951) to perform Immunohistochemistry Human - CRISP3

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Get tips on using EpiTect ChIP OneDay Kit to perform ChIP Human - AGS

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Get tips on using Re-ChIP-IT® to perform ChIP Human - LCL

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Get tips on using Gibco™DMEM/F-12 to perform Stem cell culture media Human WA09 hESC

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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 3T3-L1 fmnl 2/3

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 Rat Deletion INS-1 832/13 Ep300

Get tips on using RNeasy Plus Mini Kit to perform RNA isolation / purification Cells - immortalized HeLa, CaSki and C33A (Cervical cancer cells)

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Cellular assays Cell Isolation Hematopoietic Progenitor Cell

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