HEK293T - SPTBN1 (KO) Cell Line
Datasheet
Key Features
Cat. No.:
NTV-1225-YJ115
Species
Human
Related Disease
Neurodevelopmental disorder with speech impairment and ataxia
Summary
| Description | This HEK293T cell line features a targeted deletion of the SPTBN1 gene (βII spectrin). It is a model for studying the organization of the spectrin-based membrane skeleton and its role in cellular integrity. |
| Species | Human |
| Size | 1×10⁶ cells |
| Growth Conditions | 37°C with 5% CO₂ |
| Related Disease | Neurodevelopmental disorder with speech impairment and ataxia |
| Synonyms | HEK293T SPTBN1 Knockout cells; Spectrin Beta II-deficient HEK293T cells; HEK293T SPTBN1-null cell line; HEK293T with SPTBN1 gene knockout; SPTBN1 KO 293 cells |
| Parental cells | HEK293T |
| Format | Frozen |
| Shipping | Dry Ice |
| Storage | Store in liquid nitrogen. |
Specifications
| Mycoplasma Testing | Negative |
| Cryopreservation Medium | Can be customized |
| Research Use Only | For Research Use Only. Not For Clinical Use. |
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