Gene: SLC13A5
Official Full Name: solute carrier family 13 member 5provided by HGNC
Gene Summary: This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA03380 | SLC13A5 Knockout cell line (AC16) | Human | SLC13A5 | 1:3-1:4 | negative | Online Inquiry |
| KOA18827 | SLC13A5 Knockout cell line (BEAS-2B) | Human | SLC13A5 | 1:3~1:4 | negative | Online Inquiry |
| KOA34277 | SLC13A5 Knockout cell line (U-2932) | Human | SLC13A5 | 1:2-1:4 | negative | Online Inquiry |
| KOA49683 | SLC13A5 Knockout cell line (TPC-1) | Human | SLC13A5 | 1:5-1:8 | negative | Online Inquiry |
| KOA65086 | SLC13A5 Knockout cell line (NCM460) | Human | SLC13A5 | 1:2~1:3 | negative | Online Inquiry |
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.