siRNA / miRNA gene silencing Human MSTO-211H

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.

Get tips on using Renilla luciferase vector, pGL4.74 to perform Reporter gene assay luciferase - primary human endometrial stromal cells

Wound healing assay can be challenging due to inconsistencies and variations while making a wound on the confluent cell monolayer, consequently leads to wounds of varying sizes and widths. Moreover, this assay causes damage to the cells that are at the edge of the wound, which can prevent cell migration into the wound site and healing. The best solution is to use the standard wound healing assay kits using either combs or inserts to make a defined wound field or gap and prevent the well-to-well variation in these assays.

Get tips on using Human Melanocyte Media to perform Mammalian cell culture media HEM

Get tips on using Human vWF-A2 DuoSet ELISA to perform ELISA Human - VWF-A2

Get tips on using Human PDGF-BB ELISA Kit to perform ELISA Human - PDGF-BB

Get tips on using Human PDGF-BB DuoSet ELISA to perform ELISA Human - PDGF-BB

Get tips on using KIM-1 (human) ELISA kit to perform ELISA Human - KIM-1

Get tips on using Human IGF1 ELISA Kit (ab100545) to perform ELISA Human - IGF-I

Get tips on using HO-1 (human), ELISA kit to perform ELISA Human - HO-1