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. : AD00238Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00238Z |
| Product Type | Adenoviral particle |
| Gene | PRKD3 |
| 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 | PRKD3 protein kinase D3 [ Homo sapiens ] |
| Gene Symbol | PRKD3 |
| Synonyms | PRKD3; protein kinase D3; PRKCN, protein kinase C, nu; serine/threonine-protein kinase D3; EPK2; protein kinase EPK2; protein kinase C, nu; protein kinase C nu type; protein-serine/threonine kinase; PKD3; PRKCN; PKC-NU; nPKC-NU; |
| GeneID | 23683 |
| Uni ProtID | O94806 |
| mRNA Refseq | BC030706 |
| Chromosome Location | 2p21 |
| Function | ATP binding; metal ion binding; nucleotide binding; protein binding; protein kinase C activity; |
| Pathway | G Protein Signaling Pathways, organism-specific biosystem; IL-4 signaling Pathway, organism-specific biosystem; |
| MIM | 607077 |
The PRKD3 gene, also known as protein kinase D3, encodes a serine/threonine kinase that belongs to the protein kinase D (PKD) family. The gene plays a key role in processes such as cell proliferation, differentiation, apoptosis, and regulation of immune responses. PRKD3 is activated by diacylglycerol (DAG) and phospholipase C-coupled receptors and affects downstream signaling pathways, including NF-κB and MAPK. Dysregulation of PRKD3 has been implicated in a variety of diseases, especially cancer, where it often leads to tumor progression and metastasis. Given its critical role in cell signaling, PRKD3 is a promising target for therapeutic intervention and functional studies.
Human PRKD3 adenoviral particles are replication-defective viral vectors designed to efficiently deliver the PRKD3 gene to mammalian cells. These particles exploit the natural tropism of adenoviruses to infect a broad range of cell types, including dividing and non-dividing cells, making them ideal for in vitro and in vivo studies. This adenoviral system ensures stable and transient expression of PRKD3, allowing researchers to explore its functional role in signaling pathways, disease models, or therapeutic applications. These particles are purified and titrated to ensure consistent performance. Applications range from gain-of-function experiments to preclinical studies of gene therapy.
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The viral titer matched the specifications, and we observed minimal batch-to-batch variation. A reliable choice for repeat experiments.
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