Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
FIGURE: 1 / 1
Immunogen sequence: LNWKKACQQA QVHANLKVNN VPRSGNSALP QDPLHPGCPE NLEGILTNDV GKTGEPQSDQ QMRQEEPLPE HPQDGAKLSR KQLVLRRGLL L; Positive Samples: Rat liver; Cellular Location: Cell membrane, Multi-pass membrane protein
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function.
⚠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: FLJ10847; H+/organic cation antiporter variant 1; H+/organic cation antiporter variant 2; hMATE-1; MATE-1; MGC64822; multidrug and toxin extrusion 1; Multidrug and toxin extrusion protein 1; rMATE-1; solute carrier family 47 (multidrug and toxin extrusion), member 1; Solute carrier family 47 member 1; solute carrier family 47, member 1
Gene Aliases: MATE1; RGD1311123; SLC47A1
UniProt ID: (Human) Q96FL8, (Rat) Q5I0E9
Entrez Gene ID: (Human) 55244, (Rat) 360539
Molecular Function: transporter
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support