Gene: SLC6A5
Official Full Name: solute carrier family 6 member 5provided by HGNC
Gene Summary: This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA12385 | SLC6A5 Knockout cell line (AC16) | Human | SLC6A5 | 1:3-1:4 | negative | Online Inquiry |
| KOA27830 | SLC6A5 Knockout cell line (BEAS-2B) | Human | SLC6A5 | 1:3~1:4 | negative | Online Inquiry |
| KOA43266 | SLC6A5 Knockout cell line (U-2932) | Human | SLC6A5 | 1:2-1:4 | negative | Online Inquiry |
| KOA58644 | SLC6A5 Knockout cell line (TPC-1) | Human | SLC6A5 | 1:5-1:8 | negative | Online Inquiry |
| KOA74067 | SLC6A5 Knockout cell line (NCM460) | Human | SLC6A5 | 1:2~1:3 | negative | Online Inquiry |
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