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SLC47A1 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA525272
This item is not returnable.
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Description
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function.Specifications
SLC47A1 | |
Polyclonal | |
Unconjugated | |
Slc47a1 | |
1300013J15Rik; AI036982; FLJ10847; H+/organic cation antiporter variant 1; H+/organic cation antiporter variant 2; hMATE-1; MATE1; MATE-1; MGC64822; mMATE1; mMATE-1; multidrug and toxin extrusion 1; multidrug and toxin extrusion protein 1; RGD1311123; rMATE-1; SLC47A1; solute carrier family 47 (multidrug and toxin extrusion), member 1; solute carrier family 47 member 1; solute carrier family 47, member 1 | |
Rabbit | |
Antigen affinity chromatography, Protein A | |
RUO | |
55244 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
0.5 mg/mL | |
PBS with 0.09% sodium azide | |
Q96FL8 | |
Slc47a1 | |
KLH conjugated synthetic peptide between 492-519 amino acids from the C-terminal region of human SLC47A1 | |
400 μL | |
Primary | |
Human | |
Antibody | |
IgG |