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. : AD00255Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00255Z |
| Product Type | Adenoviral particle |
| Gene | SLC2A7 |
| Species | Human |
| 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 | SLC2A7 solute carrier family 2 (facilitated glucose transporter), member 7 [ Homo sapiens ] |
| Gene Symbol | SLC2A7 |
| Synonyms | GLUT7 |
| GeneID | 155184 |
| Uni ProtID | Q6PXP3 |
| mRNA Refseq | NM_207420.2 |
| Protein Refseq | NP_997303.2 |
| Chromosome Location | 1p36.2 |
| Function | substrate-specific transmembrane transporter activity; |
| Pathway | Class II GLUTs, organism-specific biosystem; Facilitative Na+-independent glucose transporters, organism-specific biosystem; SLC-mediated transmembrane transport, organism-specific biosystem; Transmembrane transport of small molecules, organism-specific biosystem; Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds, organism-specific biosystem; |
| MIM | 610371 |
The SLC2A7 gene encodes solute carrier family 2, member 7 (SLC2A7), a member of the facilitatory glucose transporter (GLUT) family. SLC2A7, also known as GLUT7, is primarily known for its role in the transport of monosaccharides, especially fructose, across cell membranes. Unlike other GLUT family members, SLC2A7 is highly specific for fructose and is primarily expressed in metabolically active tissues such as the liver, small intestine, and kidney. Its function is critical for nutrient absorption and energy homeostasis, making it a potential target for metabolic disorders such as diabetes and nonalcoholic fatty liver disease (NAFLD). In addition, emerging studies suggest that SLC2A7 may be involved in cancer cell metabolism, highlighting its broader physiological and pathological significance.
Human SLC2A7 adenoviral particles are genetically engineered viral vectors designed to deliver the SLC2A7 gene to target cells for functional studies or therapeutic applications. These particles are based on adenovirus, a non-enveloped DNA virus known for its high transduction efficiency, broad tropism, and stable expression of transgenes in both dividing and non-dividing cells. This adenoviral system has been modified to ensure safety by removing viral replication genes (E1/E3 deletion) and incorporating human SLC2A7 cDNA under a constitutive or tissue-specific promoter. These particles allow researchers to overexpress SLC2A7 in vitro or in vivo, facilitating the study of its role in fructose metabolism, disease pathogenesis, and potential gene therapy strategies.
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