KCNQ2 Knockout cell line (HEK293)
Catalog Number: KO36982
Price: Online Inquiry
Catalog Number: KO36982
Price: Online Inquiry
Product Information | |
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Product Name | KCNQ2 Knockout cell line (HEK293) |
specification | 1*10^6 |
Storage and transportation | Dry ice preservation/T25 live cell transportation. |
Cell morphology | Epithelioid, adherent cell |
Passage ratio | 1:3~1:6 |
species | Human |
Gene | KCNQ2 |
Gene ID | 3785 |
Build method | Electric rotation method / virus method |
Mycoplasma testing | Negative |
Cultivation system | 90%DMEM+10% FBS |
Parental Cell Line | HEK293 |
Quality Control | Genotype: KCNQ2 Knockout cell line (HEK293) >95% viability before freezing. All cells were tested and found to be free of bacterial, viruses,mycoplasma and other toxins. |
Gene Information | |
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Gene Official Full Name | potassium voltage-gated channel subfamily Q member 2provided by HGNC |
Also known as | EBN; BFNC; DEE7; EBN1; ENB1; HNSPC; KV7.2; KCNA11 |
Gene Description | The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Expression | Biased expression in brain (RPKM 15.5), adrenal (RPKM 2.3) and 1 other tissue See more |
Please note that all services are for research use only. Not intended for any clinical use.
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