Home / NGLY1 Knockout Cell Lines

NGLY1 Knockout Cell Lines

Gene: NGLY1

Official Full Name: N-glycanase 1provided by HGNC

Gene Summary: This gene encodes an enzyme that catalyzes hydrolysis of an N(4)-(acetyl-beta-D-glucosaminyl) asparagine residue to N-acetyl-beta-D-glucosaminylamine and a peptide containing an aspartate residue. The encoded enzyme may play a role in the proteasome-mediated degradation of misfolded glycoproteins. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2009]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO15760 NGLY1 Knockout cell line (HeLa) Human NGLY1 1:3~1:6 Negative Online Inquiry
KO15761 NGLY1 Knockout cell line (HCT 116) Human NGLY1 1:2~1:4 Negative Online Inquiry
KO15762 NGLY1 Knockout cell line (HEK293) Human NGLY1 1:3~1:6 Negative Online Inquiry
KO15763 NGLY1 Knockout cell line (A549) Human NGLY1 1:3~1:4 Negative Online Inquiry

Background

NGLY1 Gene Knockout Cell Lines are specialized cell line models engineered to lack the NGLY1 gene, which encodes the enzyme N-glycanase 1. This enzyme is crucial for the removal of misfolded glycoproteins, a process vital for maintaining cellular protein homeostasis. The knockout of the NGLY1 gene allows researchers to investigate the cellular consequences of impaired protein quality control, providing insights into various neurodegenerative diseases and disorders associated with protein misfolding.

These cell lines function by serving as a platform to study the downstream effect of NGLY1 deficiency, notably the accumulation of glycosylated proteins and their impact on cellular stress responses. The mechanisms involved include altered proteasomal and lysosomal activity, increased oxidative stress, and changes in apoptosis pathways. Researchers can utilize these cell lines to explore therapeutic strategies targeting these pathways, thereby contributing to the broader understanding of genetic diseases like NGLY1 deficiency, which leads to profound neurological symptoms.

The scientific importance of NGLY1 Gene Knockout Cell Lines is underscored by their applications in basic research and therapeutic development. They are invaluable for drug screening, enabling scientists to evaluate compound efficacy in restoring normal cellular function in a controlled environment. Furthermore, they allow for the identification of biomarkers relevant to NGLY1-related diseases.

In comparison to alternative cell lines that may not mimic the physiology of NGLY1 deficiency, these knockout lines offer a more accurate representation of the disease state, facilitating more pertinent research outcomes. Their lineage and specificity render them an essential tool for researchers focused on understanding glycoprotein metabolism and developing targeted therapies.

The value of NGLY1 Gene Knockout Cell Lines lies in their ability to bridge the gap between genetic understanding and clinical application. For researchers and clinicians, this innovation provides a pathway to explore new frontiers in treatment and intervention strategies. Our company is dedicated to advancing cutting-edge biological products, providing researchers with reliable tools that drive discovery and innovation in the field of genetic and molecular research.

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.