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. : AD00162Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00162Z |
| Product Type | Adenoviral particle |
| Gene | EPHA8 |
| 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 | EPHA8 EPH receptor A8 [ Homo sapiens ] |
| Gene Symbol | EPHA8 |
| Synonyms | EEK; EK3; HEK3 |
| Gene Description | EPH receptor A8 |
| GeneID | 2046 |
| Uni ProtID | P29322 |
| mRNA Refseq | NM_020526.3 |
| Protein Refseq | NP_065387.1 |
| Chromosome Location | 1p36.12 |
| Function | ATP binding; GPI-linked ephrin receptor activity; |
| Pathway | Axon guidance, organism-specific biosystem; Axon guidance, conserved biosystem; EPHA forward signaling, organism-specific biosystem; EphrinA-EPHA pathway, organism-specific biosystem; |
| MIM | 176945 |
The EPHA8 gene encodes a member of the Eph receptor tyrosine kinase family, which plays a key role in cell-cell communication, tissue patterning, and development. As members of the largest subfamily of receptor tyrosine kinases, Eph receptors and their Ephrin ligands mediate bidirectional signaling pathways that regulate cell adhesion, migration, and axon guidance. EPHA8 is closely associated with nervous system development, affecting neuronal connectivity and synaptic plasticity. In addition, EPHA8 gene dysregulation is associated with a variety of diseases, including cancer and neurological diseases. The gene is structurally conserved, with an extracellular ligand binding domain, a transmembrane region, and a cytoplasmic kinase domain, enabling it to participate in a variety of signaling cascades.
Human EPHA8 adenoviral particles are genetically engineered viral vectors designed to deliver the EPHA8 gene to target cells for research or therapeutic purposes. These particles exploit the high transduction efficiency of adenoviruses to allow stable and transient expression of EPHA8 in both dividing and non-dividing cells. The adenoviral backbone is optimized for increased safety and often lacks essential replication genes (e.g., E1/E3 regions) to prevent uncontrolled viral replication while maintaining high titers. Researchers use these particles to study the functional role of EPHA8 in signaling pathways, cellular responses, and disease mechanisms.
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We’ve replicated results over six months using different batches. The lot-to-lot consistency is impressive!
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