rna-isolation-purification-tissue-mouse-cornea

Get tips on using QIAamp BiOstic Bacteremia DNA Kit (50) to perform DNA isolation / purification Fish

Get tips on using QIAamp MinElute Virus Spin Kit (50) to perform DNA isolation / purification Viral

Get tips on using illustra GFX PCR DNA and Gel Band Purification Kits to perform

Get tips on using TruSeq Stranded mRNA to perform RNA sequencing Mouse - 3T3-L1

Get tips on using TruSeq Stranded mRNA to perform RNA sequencing Mouse - Neuro 2a

Get tips on using TruSeq Stranded mRNA to perform RNA sequencing Mouse - NSC-34

Get tips on using TruSeq Stranded mRNA to perform RNA sequencing Mouse - BV-2

Site-directed mutagenesis (SDM) can be challenging, particularly during detection/confirmation of (SDM) in colonies by sequencing or PCR techniques. This common issue in SDM is heavily relying on designing of mutagenic primer pairs. The best solution is to design the mutagenic primers that have extended 3'-ends/3'-overhang. This would provide the annealing region between the mutagenic primer pair is essentially shorter. and hence ensure a lower annealing temperature for the primer pair along with a higher chance of annealing to the template.

Get tips on using Ovation® RNA Amplification System V2 to perform Microarray RNA amplification & Labeling - Bovine olfactory nasal tissues Biotin