
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
β-1,4-Gal-T4 CRISPR/Cas9 KO Plasmid (h) | sc-407251 | 20 µg | $397.00 |
B4GALT4 encodes β-1,4-Gal-T4, a Golgi-resident β-1,4-galactosyltransferase that transfers galactose to N-acetylglucosamine to build type II lactosamine units on N- and O-linked glycans and glycolipids. Through its contribution to glycosylation, β-1,4-Gal-T4 influences protein folding, trafficking, receptor residence time, and cell–cell or cell–matrix interactions mediated by glycan-binding proteins. Altered galactosylation and lactosamine extension can reshape signaling networks and immune recognition, linking B4GALT4-dependent glycan remodeling to disease-relevant processes such as inflammation and tumor cell behavior. As part of the broader glycosyltransferase network, B4GALT4 helps define cell-surface glycome composition that impacts adhesion, migration, and differentiation programs.
β-1,4-Gal-T4 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the B4GALT4 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the B4GALT4 together with the Streptococcus pyogenes Cas9 nuclease. The plasmids also encode GFP, allowing fluorescent identification and enrichment of successfully transfected cells by fluorescence microscopy or flow cytometry.
The multi-guide design increases the likelihood of generating insertions or deletions (indels) that disrupt the B4GALT4 open reading frame following Cas9-mediated double-strand break formation. DNA breaks introduced by the CRISPR/Cas9 system are repaired through endogenous non-homologous end joining (NHEJ) pathways, frequently resulting in frameshift mutations that abolish β-1,4-Gal-T4 protein expression.
This CRISPR knockout system enables efficient generation of B4GALT4-deficient cell models for investigation of β-1,4-Gal-T4 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.