Gene: SLC16A12
Official Full Name: solute carrier family 16 member 12provided by HGNC
Gene Summary: This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA02712 | SLC16A12 Knockout cell line (AC16) | Human | SLC16A12 | 1:3-1:4 | negative | Online Inquiry |
| KOA18158 | SLC16A12 Knockout cell line (BEAS-2B) | Human | SLC16A12 | 1:3~1:4 | negative | Online Inquiry |
| KOA33608 | SLC16A12 Knockout cell line (U-2932) | Human | SLC16A12 | 1:2-1:4 | negative | Online Inquiry |
| KOA49014 | SLC16A12 Knockout cell line (TPC-1) | Human | SLC16A12 | 1:5-1:8 | negative | Online Inquiry |
| KOA64414 | SLC16A12 Knockout cell line (NCM460) | Human | SLC16A12 | 1:2~1:3 | negative | Online Inquiry |
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