ATRX Knockout cell line (MFE-280)
Catalog Number: KOA409676
Price: Online Inquiry
Catalog Number: KOA409676
Price: Online Inquiry
| Product Information | |
|---|---|
| Product Name | ATRX Knockout cell line (MFE-280) |
| specification | 1*10^6 |
| Storage and transportation | Shipped on dry ice; Store in liquid nitrogen |
| Cell morphology | Epithelial-like, adherent |
| Passage ratio | 1:2-1:3 |
| Gene | ATRX |
| Gene ID | 546 |
| Build method | Electroporation/Lentivirus |
| Mycoplasma testing | negative |
| Cultivation system | 88%MEM+10%FBS+1%NEAA+1%1%Sodium Pyruvate |
| Parental Cell Line | MFE-280 |
| Quality Control | Genotype: ATRX Knockout cell line (MFE-280)>95% viability before freezing. All cells were tested and found to be free of bacterial, viruses,mycoplasma and other toxins. |
| Gene Information | |
|---|---|
| Gene Official Full Name | ATRX chromatin remodelerprovided by HGNC |
| Also known as | JMS; XH2; XNP; MRX52; RAD54; RAD54L; ZNF-HX |
| Gene Description | The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with X-linked syndromes exhibiting cognitive disabilities as well as alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2017] |
| Expression | Ubiquitous expression in brain (RPKM 12.1), endometrium (RPKM 9.2) and 25 other tissues See more |
Please note that all services are for research use only. Not intended for any clinical use.
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