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. : AD00237Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00237Z |
| Product Type | Adenoviral particle |
| Gene | PRKD2 |
| 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 | PRKD2 protein kinase D2 [ Homo sapiens ] |
| Gene Symbol | PRKD2 |
| Synonyms | PKD2; HSPC187; nPKC-D2 |
| Gene Description | protein kinase D2 |
| Gene ID | 25865 |
| Uni Prot ID | Q9BZL6 |
| m RNA Refseq | NM_001079880.1 |
| Protein Refseq | NP_001073349.1 |
| Chromosome Location | 19q13.3 |
| MIM | 607074 |
The PRKD2 (protein kinase D2) gene encodes a serine/threonine kinase that belongs to the protein kinase D (PKD) family, which plays a key role in a variety of cellular processes including signal transduction, cell proliferation, apoptosis, and membrane trafficking. PRKD2 is activated by diacylglycerol (DAG) and phosphorylation and is typically downstream of G protein-coupled receptors (GPCRs) or receptor tyrosine kinases. It regulates key pathways such as NF-κB, MAPK, and Golgi organization, affecting cancer progression, immune responses, and cardiovascular function. Studies have shown that PRKD2 has dual roles as an oncogene and tumor suppressor, depending on the cellular context, making it a popular target for biomedical research.
Human PRKD2 adenoviral particles are replication-defective viral vectors designed to efficiently deliver the PRKD2 gene to mammalian cells. These particles exploit the natural tropism of adenoviruses to infect a variety of cell types, including dividing and non-dividing cells, making them ideal for in vitro and in vivo studies. Applications include elucidating the mechanistic role of PRKD2 in disease, screening drug candidates, and gene therapy development. Safety-enhanced designs, such as E1/E3 deletions, minimize cytotoxicity while maximizing experimental reproducibility.
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Needed to transduce multiple cell lines in parallel for an initial PRKD2 function screen. The adenovirus volume provided was sufficient, and the transduction efficiency was high across different lines (HeLa, A549, U2OS), saving us reagents and time compared to other methods.
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