SLC6A8 蛋白
(Solute Carrier Family 6 (Neurotransmitter Transporter, Creatine), Member 8 (SLC6A8))
The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008].
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4 results :
custom-made
SLC6A8
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
custom-made
SLC6A8
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for SLC6A8 蛋白
solute carrier family 6 member 8 (SLC6A8) 蛋白sodium- and chloride-dependent creatine transporter 1 (LOC473853) 蛋白
solute carrier family 6 (neurotransmitter transporter), member 8 (slc6a8) 蛋白
sodium- and chloride-dependent creatine transporter 1 (LOC100440816) 蛋白
solute carrier family 6 member 8 (Slc6a8) 蛋白
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 (Slc6a8) 蛋白
AA589632 蛋白
CCDS1 蛋白
chot1 蛋白
CHOT1 蛋白
CHT1 蛋白
creaT 蛋白
Creat 蛋白
CRT 蛋白
crtr 蛋白
CRTR 蛋白
CT1 蛋白
SLC6A8 蛋白
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