RNA isolation / purification Cells immortalized

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 hCas9 to perform CRISPR Rat - Activation CD2

Get tips on using - to perform siRNA / miRNA gene silencing Rat - IEC-6

Get tips on using pSUPER.retro.puro to perform shRNA gene silencing Rat - MM1 SSH1

Get tips on using pSUPER.retro.puro to perform shRNA gene silencing Rat - MM1 SSH2

Get tips on using pSUPER.retro.puro to perform shRNA gene silencing Rat - MM1 LIMK1

Get tips on using pSUPER.retro.puro to perform shRNA gene silencing Rat - MM1 ADF

Get tips on using lentiCRISPR to perform CRISPR Mouse - Deletion RAW 264.7 Tfeb

Get tips on using SECISBP2 Polyclonal antibody to perform Immunohistochemistry Rat - SBP2

Get tips on using HighCell# ChIP kit to perform ChIP Rat - PCCL3