ARHGEF9 Knockout cell line (A549)
Catalog Number: KO29670
Price: Online Inquiry
Catalog Number: KO29670
Price: Online Inquiry
Product Information | |
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Product Name | ARHGEF9 Knockout cell line (A549) |
specification | 1*10^6 |
Storage and transportation | Dry ice preservation/T25 live cell transportation. |
Cell morphology | Epithelioid, adherent cell |
Passage ratio | 1:3~1:4 |
species | Human |
Gene | ARHGEF9 |
Gene ID | 23229 |
Build method | Electric rotation method / virus method |
Mycoplasma testing | Negative |
Cultivation system | 90% F12K+10% FBS |
Parental Cell Line | A549 |
Quality Control | Genotype: ARHGEF9 Knockout cell line (A549) >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 | Cdc42 guanine nucleotide exchange factor 9provided by HGNC |
Also known as | DEE8; PEM2; EIEE8; PEM-2; HPEM-2; COLLYBISTIN |
Gene Description | The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. This brain-specific protein also acts as an adaptor protein for the recruitment of gephyrin and together these proteins facilitate receceptor recruitement in GABAnergic and glycinergic synapses. Defects in this gene are the cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy, as well as several other types of cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
Expression | Ubiquitous expression in brain (RPKM 18.5), heart (RPKM 6.1) and 21 other tissues See more |
Please note that all services are for research use only. Not intended for any clinical use.
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