SLC36A2, Polyclonal Antibody

Polyclonal SLC36A2; Anti-SLC36A2; Solute Carrier Family 36 Member 2; SLCA2-36; PAT2; MGC119660; TRAMD1; FLJ16051; Proton/Amino Acid Symporter 2; MGC119658; SLCA2 36; SLC36A2

For Research Use Only. Not for use in diagnostic procedures.

Polyclonal

Rabbit

Affinity purified

Lyophilized powder. Add 50ul distilled water for a 1mg/ml concentration of SLC36A2 antibody in PBS

1 mg/ml (lot specific)

Store at 2-8 degree C for short periods. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.

Small volumes of anti-SLC36A2 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Rabbit polyclonal SLC36A2 antibody

Cell Biology; Purified Polyclonal Antibodies

Western Blot (WB)

WB: 1 ug/ml

Recommended SLC36A2 Antibody Titration: 0.2-1 ug/ml

Skeletal muscle

53 kDa (MW of target protein)

solute carrier family 36 (proton/amino acid symporter), member 2

proton-coupled amino acid transporter 2

Proton-coupled amino acid transporter 2

PAT2; TRAMD1; Proton/amino acid transporter 2  [Similar Products]

S36A2_HUMAN

This gene encodes a pH-dependent proton-coupled amino acid transporter that belongs to the amino acid auxin permease 1 protein family. The encoded protein primarily transports small amino acids such as glycine, alanine and proline. Mutations in this gene are associated with iminoglycinuria and hyperglycinuria. [provided by RefSeq, Sep 2010]

SLC36A2: Involved in a pH-dependent electrogenic neuronal transport and sequestration of small amino acids. Transports glycine and proline. Inhibited by sarcosine. Defects in SLC36A2 are a cause of hyperglycinuria (HG). It is a condition characterized by excess of glycine in the urine. In some cases it is associated with renal colic and renal oxalate stones. Defects in SLC36A2 are a cause of iminoglycinuria (IG). It is a disorder of renal tubular reabsorption of glycine and imino acids (proline and hydroxyproline), marked by excessive levels of all three substances in the urine. Mutations in SLC36A2 that retain residual transport activity result in the IG phenotype only when combined with haploinsufficiency of the imino acid transporter SLC6A20 or deficiency of the neutral amino acid transporter SLC6A19. Additional polymorphisms and mutations in SLC6A18 can contribute to iminoglycinuria in some families. Belongs to the amino acid/polyamine transporter 2 family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Transporter, SLC family; Membrane protein, multi-pass; Transporter; Membrane protein, integral

Chromosomal Location of Human Ortholog: 5q33.1

Cellular Component: vacuolar membrane; plasma membrane; integral to membrane

Molecular Function: glycine transmembrane transporter activity; L-proline transmembrane transporter activity; hydrogen:amino acid symporter activity; hydrogen ion transmembrane transporter activity; L-alanine transmembrane transporter activity

Biological Process: glycine transport; proton transport; amino acid transport; ion transport; transmembrane transport; L-alanine transport

Disease: Iminoglycinuria; Hyperglycinuria

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