Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : AD00151Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00151Z |
| Product Type | Adenoviral particle |
| Gene | DEGS1 |
| Titer | Varies lot by lot, for example, ≥1x10^10 IFU/mL, ≥1x10^11 IFU/mL, ≥1x10^11 VP/mL etc. |
| Size | Varies lot by lot, for example, 100 ul, 500 ul, 1 mL etc. |
| Storage | Store at -80℃. Avoid multiple freeze/thaw cycles. |
| Shipping | Frozen on dry ice |
| Summary | Creative Biogene ensures high-quality adenovirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between adenovirus particle lots. |
| Endotoxin | Endotoxins, primarily derived from Gram-negative bacteria, can trigger adverse immune responses. Endotoxin contamination is a significant concern in adenovirus production, especially for applications in animal studies and gene therapy. Creative Biogene utilizes rigorous endotoxin detection methods to monitor the endotoxin level in our produced adenovirus particles to ensure regulatory compliance. |
| Sterility | Creative Biogene ensures that adenovirus products are free of any bacterial, fungal and other microbial contamination. |
| Ad5 E1 Detection | All Creative Biogene adenoviruses are PCR tested to ensure that there are no detectable E1 sequences in the particles, which could be from revertants or external E1 contamination. |
| RCA Assays | Adenovirus products originating at Creative Biogene are guaranteed to have undetectable replication-competent adenovirus (RCA). This quality control measure is important because there is always the possibility of wild-type contamination due to revertants or environmental sources. |
| PFU Titering | All purified adenovirus preparations are tested for infectious titer. Creative Biogene's PFU test takes a few days longer but counts true plaques in HEK cells rather than estimating PFU titers via IHC staining or TCI50 of infected cells. |
| Gene Name | DEGS1 delta(4)-desaturase, sphingolipid 1 [ Homo sapiens ] |
| Gene Symbol | DEGS1 |
| Synonyms | MLD; DEGS; DES1; Des-1; FADS7; MIG15; DEGS-1 |
| GeneID | 8560 |
| Uni ProtID | O15121 |
| mRNA Refseq | NM_003676.3 |
| Protein Refseq | NP_003667.1 |
| Chromosome Location | 1q42.11 |
| Function | electron carrier activity; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen; |
| Pathway | Ceramide biosynthesis, organism-specific biosystem; Ceramide biosynthesis, conserved biosystem; Metabolism, organism-specific biosystem; Metabolism of lipids and lipoproteins, organism-specific biosystem; Phospholipid metabolism, organism-specific biosystem; Sphingolipid de novo biosynthesis, organism-specific biosystem; Sphingolipid metabolism, organism-specific biosystem; |
The DEGS1 gene (Delta(4)-desaturase, sphingolipid 1) encodes a key enzyme in the sphingolipid biosynthesis pathway that specifically catalyzes the conversion of dihydroceramide to ceramide. This step is essential for maintaining cellular sphingolipid homeostasis, which affects membrane integrity, signal transduction, and apoptosis. Dysregulation of the DEGS1 gene has been implicated in a variety of diseases, including neurodegenerative diseases, cancer, and metabolic syndrome. Its role in regulating ceramide levels makes it a potential therapeutic target, as ceramide is involved in cellular stress responses and proliferation.
Human DEGS1 adenoviral particles are engineered viral vectors designed to deliver the DEGS1 gene to target cells for overexpression studies. These particles utilize adenoviral technology, which allows for high transduction efficiencies in a variety of cell types, including primary and dividing cells. The adenoviral system ensures stable and transient gene expression, making it ideal for functional analyses, such as studying the role of DEGS1 in sphingolipid metabolism or its effects on disease models. These particles are typically replication-defective, which improves safety by preventing uncontrolled spread of the virus. They can be used for in vitro and in vivo applications, such as gene therapy research or the study of ceramide-related pathological mechanisms.
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Even in hard-to-transfect cells, these particles achieved strong gene expression. Minimal optimization was needed—great out-of-the-box performance.
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