Recombinant Human SLC7A7 cell lysate SLC7A7-1639HCL

Cat.No.:	SLC7A7-1639HCL
Description:	The protein encoded by this gene is the light subunit of a cationic amino acid transporter. This sodium-independent transporter is formed when the light subunit encoded by this gene dimerizes with the heavy subunit transporter protein SLC3A2. This transporter is found in epithelial cell membranes where it transfers cationic and large neutral amino acids from the cell to the extracellular space. Defects in this gene are a cause of lysinuric protein intolerance (LPI). Several transcript variants encoding the same protein have been found for this gene.
Species:	Human
Size:	100 ul
Storage Buffer:	1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications:	Western Blot;

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Gene Name:	SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 [ Homo sapiens ]
Official Symbol:	SLC7A7
Synonyms:	SLC7A7; solute carrier family 7 (amino acid transporter light chain, y+L system), member 7; LPI; Y+L amino acid transporter 1; y+LAT 1; monocyte amino acid permease 2; y(+)L-type amino acid transporter 1; solute carrier family 7 (cationic amino acid transporter, y+ system), member 7; LAT3; MOP-2; Y+LAT1; y+LAT-1;
Gene ID:	9056
mRNA Refseq:	NM_001126105
Protein Refseq:	NP_001119577
MIM:	603593
UniProt ID:	Q9UM01
Chromosome Location:	14q11.2
Pathway:	Amino acid transport across the plasma membrane, organism-specific biosystem; Basigin interactions, organism-specific biosystem; Cell surface interactions at the vascular wall, organism-specific biosystem; Hemostasis, organism-specific biosystem; Protein digestion and absorption, organism-specific biosystem; Protein digestion and absorption, conserved biosystem; SLC-mediated transmembrane transport, organism-specific biosystem;
Function:	amino acid transmembrane transporter activity;