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Recommended positive controls: 293T, A431.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
The SLC22A18/SLC22A18AS genes are a sense-antisense pair located at human chromosome segment 11p15.5. These genes are paternally imprinted: paternal alleles are silenced and maternal alleles are expressed. SLC22A18AS (antisense) is associated to SLC22A18 (sense). These two genes share, in divergent orientations, 31 bp in their 5' regions (between the first exon of SLC22A18AS and the second exon of SLC22A18).
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Beckwith-Wiedemann region 1B; Beckwith-Wiedemann syndrome chromosome region 1, candidate b; organic cation transporter-like 2 antisense; organic cation transporter-like protein 2 antisense protein; p27-Beckwith-Wiedemann region 1 B; solute carrier family 22 (organic cation transporter), member 1-like antisense; solute carrier family 22 (organic cation transporter), member 18 antisense; solute carrier family 22 member 1-like antisense protein; solute carrier family 22 member 18 antisense protein
Gene Aliases: BWR1B; BWSCR1B; ORCTL2S; p27-BWR1B; SLC22A1LS
Entrez Gene ID: (Human) 5003
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