Microarray Gene expression arrays A-375 human melanoma

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DNA-protein interactions are studied by using ChIP. The basic steps in this technique are crosslinking, sonication, immunoprecipitation, and analysis of the immunoprecipitated DNA. During ChIP, if chromatin is under-fragmented or fragments are too large which can lead to the increased background and lower resolution. Shorter cross-linking times (5-10 min) and/or lower formaldehyde concentrations (<1%) may improve shearing efficiency. If Chromatin is over-fragmented, then optimize shearing conditions for each cell type to improve ChIP efficiency. Over-sonication of chromatin may disrupt chromatin integrity and denature antibody epitopes. If you do not see any product or very little product in the input PCR reactions, add 5–10 μg chromatin per IP.

Proteins ChIP Human SW480

Get tips on using Human/Mouse NLRP3/NALP3 Antibody to perform Western blotting NLRP3

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Get tips on using Human/Mouse/Rat SOX2 Antibody to perform Western blotting SOX2

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Get tips on using Human Ubiquitin/Ubiquitin+1 Antibody to perform Western blotting Ubiquitin

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Get tips on using Human BDNF ELISA Kit (ab212166) to perform ELISA Mouse - BDNF

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Get tips on using Human SCF ELISA Kit (ab100636) to perform ELISA Rat - SC

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Get tips on using Human TNF Alpha PicoKine™ ELISA Kit to perform ELISA Human - TNF-alpha

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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 Human Activation interferon-γ promoter

Get tips on using Human Lipocalin-2 ELISA Kit (NGAL) (ab119600) to perform ELISA Human - NGAL/LCN2

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