siRNA / miRNA gene silencing Rat NPC

- Found 4908 results

Get tips on using Rat Gastrin ELISA Kit to perform ELISA Rat - Gastrin

Products Cusabio Rat Gastrin ELISA Kit

Get tips on using BDNF Rat ELISA Kit to perform ELISA Rat - BDNF

Products Thermo Fisher Scientific BDNF Rat ELISA Kit

Get tips on using Rat Activin-A ELISA to perform ELISA Rat - Activin

Products Raybiotech Rat Activin-A ELISA

Get tips on using Rat Adiponectin ELISA Kit to perform ELISA Rat - Adiponectin

Products Sigma-Aldrich Rat Adiponectin ELISA Kit

Get tips on using Tf (Rat) ELISA Kit to perform ELISA Rat - Transferrin (Tf)

Products Abnova Tf (Rat) ELISA Kit

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.

DNA Site Directed Mutagenesis (SDM) Rat Point mutation Rat-2 PIK3CB

Get tips on using mirVana™ miRNA Isolation Kit, with phenol to perform RNA isolation / purification Cells - primary rat aortic smooth muscle cells

Products Thermo Fisher Scientific mirVana™ miRNA Isolation Kit, with phenol

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 Activation CD38

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 Activation CD2

Get tips on using β-Galactosidase Reporter Gene Staining Kit to perform Reporter gene assay β-galactosidase substrates - rat mesenchymal stem cells (MSCs)

Products Sigma-Aldrich β-Galactosidase Reporter Gene Staining Kit

Outsource your experiment

Fill out your contact details and receive price quotes in your Inbox

  Outsource experiment
Become shareholder Discussions About us Contact Privacy Terms