GLDN Knockout cell line (TPC-1)
Catalog Number: KOA49308
Price: Online Inquiry
Catalog Number: KOA49308
Price: Online Inquiry
| Product Information | |
|---|---|
| Product Name | GLDN Knockout cell line (TPC-1) |
| specification | 1*10^6 |
| Storage and transportation | Shipped on dry ice; Store in liquid nitrogen |
| Cell morphology | Epithelial-like, adherent |
| Passage ratio | 1:5-1:8 |
| species | Human |
| Gene | GLDN |
| Gene ID | 342035 |
| Build method | Electroporation/Lentivirus |
| Mycoplasma testing | negative |
| Cultivation system | 90%DMEM+10%FBS |
| Parental Cell Line | TPC-1 |
| Quality Control | Genotype: GLDN Knockout cell line (TPC-1)>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 | gliomedinprovided by HGNC |
| Also known as | CLOM; COLM; CRGL2; CRG-L2; LCCS11; UNC-112; UNC-122 |
| Gene Description | This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017] |
| Expression | Biased expression in brain (RPKM 4.5), fat (RPKM 3.3) and 12 other tissues See more |
Please note that all services are for research use only. Not intended for any clinical use.
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