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. : AD00243Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | AD00243Z |
| Product Type | Adenoviral particle |
| Gene | RBL1 |
| 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 | RBL1 retinoblastoma-like 1 (p107) [ Homo sapiens ] |
| Gene Symbol | RBL1 |
| Synonyms | PRB1; p107; CP107 |
| Gene Description | retinoblastoma-like 1 (p107) |
| Gene ID | 5933 |
| Uni Prot ID | P28749 |
| m RNA Refseq | NM_183404.1 |
| Protein Refseq | NP_899662.1 |
| Chromosome Location | 20q11.2 |
| Pathway | Adipogenesis, organism-specific biosystem; Cell Cycle, organism-specific biosystem; Cell Cycle, Mitotic, organism-specific biosystem; Cell cycle, organism-specific biosystem; Cell cycle, organism-specific biosystem; Cell cycle, conserved biosystem; Cyclin D associated events in G1, organism-specific biosystem; |
| MIM | 116957 |
The RBL1 gene, also known as retinoblastoma-like gene 1 or p107, encodes a key member of the retinoblastoma (RB) family of proteins and plays a key role in cell cycle regulation and tumor suppression. RBL1 acts as a transcriptional co-repressor that binds to the E2F transcription factor to repress the expression of genes required for cell cycle progression, particularly during the G1 phase. This regulatory mechanism ensures normal cell division and prevents uncontrolled proliferation, a hallmark of cancer. RBL1 is highly expressed in differentiated tissues and has overlapping but distinct functions from other RB family members, such as RB1 and RBL2 (p130). Furthermore, dysregulation of RBL1 has been implicated in a variety of cancers.
Human RBL1 adenoviral particles are engineered viral vectors designed to efficiently deliver the RBL1 gene to target cells. Adenoviral vectors are widely used in molecular biology due to their high transduction efficiency, broad tropism, and ability to infect both dividing and non-dividing cells. These particles are replication-defective, which allows for stable transgene expression while ensuring safety. The researchers used human RBL1 adenoviral particles to study the role of this gene in cell cycle regulation, apoptosis, and tumor suppression, and to explore its potential therapeutic applications in cancer treatment.
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