Transfected Stable Cell Lines
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Cat. No. : AD00233Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00233Z |
| Product Type | Adenoviral particle |
| Gene | PPP1CB |
| 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 | PPP1CB protein phosphatase 1, catalytic subunit, beta isozyme [ Homo sapiens ] |
| Gene Symbol | PPP1CB |
| Synonyms | PP-1B; PPP1CD; PP1beta |
| Gene Description | protein phosphatase 1, catalytic subunit, beta isoform |
| GeneID | 5500 |
| Uni ProtID | P62140 |
| mRNA Refseq | NM_002709.2 |
| Protein Refseq | NP_002700.1 |
| Chromosome Location | 2p23 |
| Pathway | Alcoholism, organism-specific biosystem; Alcoholism, conserved biosystem; Amphetamine addiction, organism-specific biosystem; Amphetamine addiction, conserved biosystem; Dopaminergic synapse, organism-specific biosystem; Dopaminergic synapse, conserved biosystem; Downregulation of TGF-beta receptor signaling, organism-specific biosystem; |
| MIM | 600590 |
The PPP1CB gene encodes the catalytic subunit of protein phosphatase 1 beta (PP1β), a key serine/threonine phosphatase involved in a variety of cellular processes including signal transduction, cell cycle regulation, and metabolism. As a member of the PP1 family, PP1β functions by dephosphorylating target proteins, thereby regulating their activity and ensuring cellular homeostasis. PPP1CB interacts with numerous regulatory subunits to form a holoenzyme with distinct substrate specificities, enabling it to participate in pathways such as glycogen metabolism, neuronal signaling, and muscle contraction. Dysregulation of PPP1CB has been implicated in diseases such as cancer, neurodegenerative disorders, and cardiovascular disease.
Human PPP1CB Adenoviral Particles are recombinant adenoviral vectors designed to deliver the PPP1CB gene to mammalian cells for overexpression studies. These particles take advantage of the high transduction efficiency and broad tropism of adenovirus, making them ideal for both dividing and non-dividing cells. The adenoviral backbone is designed to be replication-defective, ensuring biosafety while maintaining high transduction rates. Applications include exploring the role of PPP1CB in cell signaling, disease mechanisms, or potential gene therapy approaches.
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The adenoviral particles worked flawlessly in our lab. The transduction efficiency was excellent, and we observed strong PPP1CB expression in our target cells. Highly recommended!
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