PTPRS Knockout cell line (AC16)
Catalog Number: KOA14013
Price: Online Inquiry
Catalog Number: KOA14013
Price: Online Inquiry
| Product Information | |
|---|---|
| Product Name | PTPRS Knockout cell line (AC16) |
| specification | 1*10^6 |
| Storage and transportation | Shipped on dry ice; Store in liquid nitrogen |
| Cell morphology | Fibroblast-like, adherent |
| Passage ratio | 1:3-1:4 |
| species | Human |
| Gene | PTPRS |
| Gene ID | 5802 |
| Build method | Electroporation/Lentivirus |
| Mycoplasma testing | negative |
| Cultivation system | 90% DMEM/F12+10% FBS |
| Parental Cell Line | AC16 |
| Quality Control | Genotype: PTPRS Knockout cell line (AC16)>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 | protein tyrosine phosphatase receptor type Sprovided by HGNC |
| Also known as | R-PTP-S; PTPSIGMA; PTP-sigma; R-PTP-sigma |
| Gene Description | The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular region, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this protein is composed of multiple Ig-like and fibronectin type III-like domains. Studies of the similar gene in mice suggested that this PTP may be involved in cell-cell interaction, primary axonogenesis, and axon guidance during embryogenesis. This PTP has been also implicated in the molecular control of adult nerve repair. Four alternatively spliced transcript variants, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008] |
| Expression | Broad expression in fat (RPKM 30.9), brain (RPKM 23.8) and 23 other tissues See more |
Please note that all services are for research use only. Not intended for any clinical use.
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