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. : CSC-RO01166 Host Cell : BEAS-2B
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01166 |
| Description | BEAS-2B-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in BEAS-2B-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, BEAS-2B-Cas9 cell line can be used to efficiently generate targeted genomic modifications including gene knockout, gene knockin, gene mutagenesis, gene tagging etc. It is also an ideal cell line model for sgRNA screening and validation, either individually or in pools. |
| Introduction | Clustered regularly interspaced palindromic repeats (CRISPR)/Cas9 is a gene-editing technology that contains two essential components: a guide RNA (gRNA) to match a target gene, and the Cas9 (CRISPR-associated protein 9) endonuclease which causes a double-stranded DNA break, allowing modifications to the genome via nonhomologous end joining (NHEJ) or homology-directed repair (HDR). |
| Product Type | Cas9 overexpression stable cell line |
| Target Gene | Cas9 |
| Host Cell | BEAS-2B |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1) CRISPR genome editing, such as gene knockout (KO), gene knockin (KI), gene mutagenesis, gene tagging etc. 2) High-throughput sgRNA screening and validation |
| Size | One vial of frozen cells, typically >1x106 cells/vial |
| Validation | T7 Endonuclease I assay |
| Quality Control |
1) T7E1 assay 2) Mycoplasma detection |
| Storage | Liquid nitrogen |
| Shipping | Dry ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
| Target Gene | Cas9 |
The Cas9-stable cell line BEAS-2B is a genetically engineered cell line derived from BEAS-2B human bronchial epithelial cells. BEAS-2B cells are derived from normal human bronchial epithelium and immortalized through transformation with adenovirus 12-SV40 hybrid virus, making them an important model for respiratory system research. In this stable cell line, the CRISPR-associated protein 9 (Cas9) nuclease is constitutively expressed under the regulation of a strong promoter, enabling highly efficient and targeted genome editing. Cas9 integration into the BEAS-2B genome ensures the stability of Cas9 protein expression during cell passaging, eliminating the need for repeated transfection. Its epithelial origin and relevance to lung biology make it particularly suitable for research involving airway diseases, toxicology, and the functional analysis of genes in the human respiratory system.
The Cas9-stable cell line BEAS-2B is primarily used for high-throughput CRISPR screening to identify gene functions in the respiratory pathway, enabling researchers to knock out specific genes associated with lung cancer, asthma, or chronic obstructive pulmonary disease (COPD) by introducing guide RNA (gRNA). This accelerates the validation of drug targets because genes associated with disease mechanisms can be systematically disrupted, allowing for the assessment of phenotypic effects and therapeutic vulnerabilities. In toxicology, this cell line can be used to study environmental pollutants (such as cigarette smoke or nanoparticles) by editing genes involved in oxidative stress or inflammatory responses. Furthermore, it supports the construction of homologous disease models—such as introducing oncogenic mutations to mimic lung cancer development—for preclinical drug testing. Beyond basic research, this cell line also plays a crucial role in the development of gene therapies, the optimization of CRISPR delivery methods, and the study of host-pathogen interactions in respiratory infections.
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