Immunohistochemistry CD31 Rabbit Rat

Get tips on using CD326 (EpCAM) Monoclonal Antibody (G8.8), eFluor 450, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD326/EpCAM

Get tips on using CD137 (4-1BB) Monoclonal Antibody (17B5), eFluor 450, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD137

Get tips on using CD36 Monoclonal Antibody (eBioNL07 (NL07)), PerCP-eFluor 710, eBioscience™ to perform Flow cytometry Anti-bodies Human - CD36/CB38

Get tips on using FITC anti-mouse CD3ε Antibody to perform Flow cytometry Anti-bodies Mouse - CD3

Get tips on using CD3e Monoclonal Antibody (145-2C11), Biotin, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD3

Get tips on using Human Syndecan-1 ELISA Kit (CD138) (ab46506) to perform ELISA Human - SDC1

Get tips on using EasySep™ Human CD33 Positive Selection Kit II to perform Cell Isolation Monocyte

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.