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Synapsin-iCre Lentivirus

Synapsin-iCre Lentivirus

Cat.No. :  LV00980Z

Titer: ≥1*10^7 TU/mL / ≥1*10^8 TU/mL / ≥1*10^9 TU/mL Size: 100 ul/500 ul/1 mL

Storage:  -80℃ Shipping:  Frozen on dry ice

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Lentivirus Particle Information

Quality Control

Cat. No. LV00980Z
Description This lentivirus contains iCre (codon-improved Cre) under the control of human synapsin promoter.
Target Gene iCre
Titer Varies lot by lot, for example, ≥1*10^7 TU/mL, ≥1*10^8 TU/mL, ≥1*10^9 TU/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
Creative Biogene ensures high-quality lentivirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between lentivirus particle lots.
Mycoplasma Creative Biogene routinely tests for mycoplasma contamination using a mycoplasma detection kit. Cell lines are maintained for approximately 20 passages before being discarded and replaced with a new vial of early passage cells. Approximately 2 weeks after thawing, cell culture supernatants are tested for mycoplasma contamination. Creative Biogene ensures that lentiviral products are free of mycoplasma contamination.
Purity Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared lentiviral vectors to ensure they meet quality standards.
Sterility The lentiviral samples were inoculated into cell culture medium for about 5 days and the growth of bacteria and fungi was tested. Creative Biogene ensures that the lentiviral products are free of microbial contamination.
Transducibility Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of lentivirus to deliver genetic material into target cells, and assess gene expression and functional activities.
Proviral Identity Confirmation All Creative Biogene lentiviral vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the lentiviral vector, harvesting the cells a few days later, and isolating genomic DNA. This DNA is then used as a template to amplify a portion of the expected lentiviral insert.
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Principles of lentiviral infection 1. Recognition and binding of viruses to cells: Lentivirus particles carry specific glycoproteins (such as VSV-G) on their surface, which can recognize and bind to specific receptors on the surface of host cells. This recognition process is highly specific, ensuring that the virus can accurately infect the target cell. 2. Virus enters the cell: Once the virus binds to the cell surface receptor, the virus particles enter the cell through endocytosis. During endocytosis, the virus particles are encapsulated in a vesicle called an endosome, and then the viral envelope fuses with the endosome membrane to release the viral genetic material (RNA) into the cytoplasm. 3. Reverse transcription process: Lentivirus is an RNA virus whose genetic material is single-stranded RNA. In the cytoplasm, the viral RNA is transcribed into double-stranded DNA (cDNA) under the action of reverse transcriptase. This process is a key step in viral replication, which allows the viral genetic information to exist in the form of DNA, facilitating subsequent integration into the host cell genome. 4. Integration of viral DNA into the host cell genome: The cDNA generated by reverse transcription is transported into the cell nucleus and integrated into the host cell genome under the action of integrase. The integration process is achieved by recombination of specific sequences at both ends of the viral DNA (called long terminal repeats, LTR) with specific locations of the host cell genome. Once the integration is complete, the viral DNA becomes part of the host cell genome and replicates as the host cell divides. 5. Expression of exogenous genes: After integration into the host cell genome, the exogenous genes in the viral DNA (i.e., the target genes inserted) will begin to express under the regulation of the host cell's transcription and translation systems. Since the exogenous gene has been integrated into the host cell genome, it can continue to express as the host cell divides, achieving long-term and stable gene expression effects.
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