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. : GK-0003
| Cat. No. | GK-0003 |
| Description | Leveraging two major technology platforms—KASP (Kompetitive Allele-Specific PCR) and TaqMan MGB probes—we provide cost-effective or ultra-high-specificity custom genotyping services for any species and any genetic locus. |
| Introduction | If the customer provides a specific genotyping RS number, we can perform custom development and offer SNP testing services upon receipt of mailed blood/tissue/cell samples. The customer needs to provide: 1. Sample materials such as cells (≥10^6 cells), tissue (≥300 mg), blood (≥1 ml), serum (≥1.5 ml), etc.; nucleic acid extraction is charged separately; 2. Genomic DNA (volume ≥30 μl, concentration ≥50 ng/μl), with purity OD260/280 between 1.7 and 1.9; 3. For the human genome, the RS number of the SNP locus must be provided. For other species without rs numbers, such as cattle, chickens, and fish, the exact 200 bp sequences flanking both upstream and downstream of the SNP locus must be provided, along with the mutation type at the SNP locus and whether any other linked loci exist within 25 bp upstream or downstream of the locus. We deliver: 1. SNP results (Excel spreadsheet); 2. Complete experimental report: amplification and reaction systems, primers involved, and probe sequences; Scatter plot of clustering results (KASP method) / Amplification curves and Ct value analysis (TaqMan MGB method). 3. Other relevant materials required by the customer. |
| Gene | TSPO |
| Features | Genotyping Accuracy >99% |
| Applications | Research Use |
| Size | Box |
| Format | 100T |
| Note | All SNP kits are custom-developed and not available from stock. Primers and probes are individually designed and synthesized based on the RS numbers or target sequences provided by the customer. |
| Storage | -20℃ |
The TSPO gene encodes an 18 kDa translocator protein on the mitochondrial outer membrane and is a key biomarker of neuroinflammatory activation. Genetic polymorphisms at specific loci directly affect the binding affinity between TSPO and PET tracers, thereby determining the accuracy and reliability of neuroinflammation imaging. In Alzheimer's disease research, although genotyping of this locus is not directly associated with disease susceptibility, it is decisive for TSPO-PET neuroinflammation imaging: approximately 30% of the population, due to low-affinity genotypes, cannot obtain valid imaging data with conventional tracers, potentially leading to biased neuroinflammation assessment or failed examinations. Pre-screening via an SNP genotyping detection kit can precisely identify high-, medium-, and low-affinity types, guiding clinicians to select appropriate tracers or perform signal correction, ensuring the accuracy of Alzheimer's disease neuroinflammation assessment and providing a reliable molecular imaging basis for early disease diagnosis, disease course monitoring, and anti-inflammatory treatment efficacy evaluation. With the development of novel cross-genotype tracers and the establishment of the ATN+I diagnostic framework, genotyping detection of this locus will become a standard pre-procedure for precise imaging diagnosis of Alzheimer's disease, playing a core value in early screening of neurodegenerative diseases, individualized treatment strategy development, and subject stratification in new drug clinical trials, promoting a comprehensive transformation of Alzheimer's disease from pathological diagnosis to the era of precision medicine.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
Write a review of your use of Biogene products and services in your research. Your review can help your fellow researchers make informed purchasing decisions.