Protein Assays

Solute carrier family 25 member 26 (SLC25A26), spanning 135kb of the human genome with nine exons and eight introns, is mapped to human chromosome 3p14.3.

Solute carrier family 25, member 39 (SLC25A39, CGI69) is a member of the SLC25 carrier family that mediates transport across the inner mitochondrial membrane. SLC25A39 may be involve in the incorporation of iron into protoporphyrin IX, an essential

Solute carrier family 25, member 39 (SLC25A39), also called as CGI-69, with 318 amino acids is encoded by a gene with 11 exons mapped to human chromosome 17. SLC family proteins are expressed abundantly in central nervous system (CNS).

Solute carrier family 36 member 4 (SLC36A4) is a sodium-independent amino acid transporter which is present in lysosomes, endosomes and the plasma membrane. The gene encoding SLC36A4 is localized on chromosome 11.

SLC37A2 (solute carrier family 37, member 2) is a phosphate (P i )-associated antiporter, which resides in the endoplasmic reticulum (ER). It is a member of the solute carrier 37 (SLC37) family, which consists of four members.

Immunogen Synthetic peptide directed towards the C terminal region of human SLC47A2 Biochem/physiol Actions SLC47A2 is a protein belonging to a family of transporters involved in excretion of toxic electrolytes, both endogenous and exogenous,

General description The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin

Anti-SMIM21 small integral membrane protein 21, 25ul UN 1687

Immunogen spermine oxidase Application All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

Anti-SMURF1 SMAD specific E3 ubiquitin protein ligase 1, 25u

SNN (stannin) is a mitochondrial membrane protein, which has a membrane helical region, a linker region containing conserved CXC metal-binding motif, a predictive 14-3-3&#950 binding domain and a cytosolic helical region. This gene is localized to

The gene SPATA3 (spermatogenesis-associated protein 3) has been mapped to human chromosome 2q37. The gene encodes a testis-specific protein.