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. : AD00232Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00232Z |
| Product Type | Adenoviral particle |
| Gene | PPP1CA |
| 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 | PPP1CA protein phosphatase 1, catalytic subunit, alpha isozyme [ Homo sapiens ] |
| Gene Symbol | PPP1CA |
| Synonyms | PP-1A; PPP1A; PP1alpha |
| Gene Description | protein phosphatase 1, catalytic subunit, alpha isoform |
| GeneID | 5499 |
| Uni ProtID | P62136 |
| mRNA Refseq | NM_002708.3 |
| Protein Refseq | NP_002699.1 |
| Chromosome Location | 11q13 |
| Pathway | ALK1 signaling events, organism-specific biosystem; Alcoholism, organism-specific biosystem; Alcoholism, conserved biosystem; Amphetamine addiction, organism-specific biosystem; Amphetamine addiction, conserved biosystem; BMP receptor signaling, organism-specific biosystem; DARPP-32 events, organism-specific biosystem; |
| MIM | 176875 |
The PPP1CA gene encodes protein phosphatase 1 catalytic subunit alpha (PP1α), a key serine/threonine phosphatase involved in regulating multiple cellular processes including cell cycle progression, metabolism, and signal transduction. As one of the major isoforms of PP1, PP1α is able to dephosphorylate target proteins to regulate their activity, thereby maintaining cellular homeostasis. Dysregulation of PPP1CA has been implicated in a variety of diseases, such as cancer, neurodegenerative diseases, and cardiovascular diseases, highlighting its critical role in maintaining physiological balance. Research on PPP1CA has often focused on understanding its regulatory mechanisms and its interactions, making it a key target for therapeutic and functional studies.
Human PPP1CA Adenoviral Particles are genetically engineered recombinant adenovirus designed to deliver the PPP1CA gene into mammalian cells for overexpression studies. These viral particles take advantage of the high transduction efficiency and broad tropism of adenoviral vectors to ensure stable gene delivery in both dividing and non-dividing cells. These viral particles are replication-defective, enhancing safety for in vitro and in vivo applications. They are ideal for studying the functional role of PP1α, pathway analysis, or rescuing phenotypes in PPP1CA-deficient models. They are purified and titrated to ensure consistent performance, providing researchers with a reliable tool for gene therapy exploration, mechanistic studies, or drug screening.
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Unlike other viral vectors we’ve tried, these particles showed minimal cytotoxicity even at higher MOIs. The purified prep was clean, with no off-target effects.
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