Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : AD00220Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00220Z |
| Product Type | Adenoviral particle |
| Gene | NUPR1 |
| 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 | NUPR1 nuclear protein, transcriptional regulator, 1 [ Homo sapiens ] |
| Gene Symbol | NUPR1 |
| Synonyms | P8; COM1 |
| Gene Description | nuclear protein 1 |
| GeneID | 26471 |
| Uni ProtID | O60356 |
| mRNA Refseq | NM_001042483.1 |
| Protein Refseq | NP_001035948.1 |
| Chromosome Location | 16p11.2 |
| Function | chromatin binding; molecular_function; |
| Pathway | Transcriptional misregulation in cancer, organism-specific biosystem; Transcriptional misregulation in cancer, conserved biosystem; |
| MIM | 614812 |
NUPR1 (nuclear protein 1, also known as p8 or Com1) is a highly conserved, small molecule stress-induced gene that plays a key role in cellular responses to stress, inflammation, and cancer. Encoded by a single exon, NUPR1 is ubiquitously expressed and functions as a transcriptional regulator, influencing pathways associated with apoptosis, autophagy, and endoplasmic reticulum (ER) stress. Its expression is upregulated in a variety of pathological conditions, including pancreatic ductal adenocarcinoma (PDAC), liver fibrosis, and neurodegenerative diseases. NUPR1 is involved in tumor progression, metastasis, and chemoresistance, making it a promising target for therapeutic intervention.
Human NUPR1 Adenoviral Particles are genetically engineered viral vectors designed to deliver the NUPR1 gene to target cells for functional studies or therapeutic applications. These particles are based on a replication-defective adenovirus, which ensures efficient transduction into a variety of dividing and non-dividing cells while minimizing cytotoxicity. This adenoviral system has high transduction efficiency and stable transgene expression, making it ideal for in vitro and in vivo studies. They are particularly valuable in cancer research, as the dual role of NUPR1 as a stress adaptor and oncogenic driver requires precise manipulation. In addition, these particles are routinely purified and titrated to ensure consistency in experimental results, supporting applications in gene therapy development and mechanistic studies.
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