CRISPR Mouse Deletion Neuro 2a

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When extracting nucleic acids from cell cultures, thorough homogenization of cells via vortexing in lysis buffer is very necessary. Choose the best RNA isolation method keeping in mind the downstream applications, generally, column-based isolations result in clean and concentrated RNA samples. Downstream applications like sequencing and cDNA synthesis require high-quality RNA, always treat the samples with DNases and check their integrity by running a gel.

RNA RNA isolation / purification Cells primary mouse tracheal epithelial cells

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Repression HBV RT

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Get tips on using lentiCRISPR v2 to perform CRISPR Human - Activation α-synuclein

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Get tips on using lentiCRISPR v2 to perform CRISPR Human - Repression miR-21

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Get tips on using lenti dCAS-VP64_Blast to perform CRISPR Human - Activation ASCL1

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Get tips on using lenti dCAS-VP64_Blast to perform CRISPR Human - Activation RhoGDIα

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Get tips on using M-ST1n-VP64 to perform CRISPR Human - Activation RHOXF2

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Get tips on using M-ST1n-VP64 to perform CRISPR Human - Activation MIAT

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Get tips on using pSLQ1658-dCas9-EGFP to perform CRISPR Human - Activation BRCA1

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Get tips on using pcDNA-dCas9-VP64 to perform CRISPR Human - Activation REPRIMO

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