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|Background:||SLC6A8, also known as CRTR, CT1, or CRT, belongs to the Na+- and Clâ€“- dependent neurotransmitter transporter family and transports creatine in the brain and muscles. Since muscle cells do not synthesize creatine, they must take it up via SLC6A8. Missense mutations in the SLC6A8 gene result in the X-linked creatine deficiency syndrome, which is characterized by mental retardation and physical developmental disorders due to a defect in creatine metabolism.|
|Gene ID Human:||6535|
|Gene ID Mouse:||102857|
|Regulatory Statement:||For Research Use Only. Not for use in diagnostic procedures.|
|Product Type:||Primary Antibody|
There are no additional documents for Anti-SLC6A8/CRTR polyclonal antibody Trial size at this time.
There are no references for Anti-SLC6A8/CRTR polyclonal antibody Trial size at this time.