S47A1 rabbit pAb
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008],
Product Specifications
Background
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]
Product Name Alternative
Multidrug and toxin extrusion protein 1 (MATE-1) (hMATE-1) (Solute carrier family 47 member 1)
UniProt
Q96FL8
Swiss Prot
Q96FL8
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human S47A1 AA range: 158-208
Target
S47A1
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Molecular Weight
65kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
65kD
Fragment
IgG
Subcellular Location
Cell membrane ; Multi-pass membrane protein . Predominantly localized at the plasma membrane but also found in intracellular organelles.
Other Product Names
Multidrug and toxin extrusion protein 1 (MATE-1) (hMATE-1) (Solute carrier family 47 member 1)
Gene ID (Human)
55244
Available Sizes
Curated Selection
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
E3224-02-PE 200 µL
ENPP2, ID (K416) (Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 2, E-NPP 2, Extracellular Lysophospholipase D, LysoPLD, Autotaxin, ATX, PDNP2) (PE) discontinued
Ask
View Details 
