The SLC16A12 Antibody (PAC01241) is a powerful tool for research involving the SLC16A12 protein, a member of the solute carrier family known for its role in transporting metabolites across cell membranes. This polyclonal antibody, developed using advanced techniques, shows high specificity and sensitivity in detecting SLC16A12 in human samples.The SLC16A12 Antibody is ideal for use in Western blot applications, enabling researchers to study the expression and function of SLC16A12 in various cell types. By binding specifically to the SLC16A12 protein, this antibody facilitates the detection and analysis of SLC16A12, making it a valuable tool for investigations in metabolism, transporter biology, and related fields.
SLC16A12 is a key player in cellular metabolism and energy balance, making it a potential target for therapeutic interventions in metabolic disorders and related conditions. Research on SLC16A12 has the potential to unveil new insights into metabolic pathways and may lead to the development of novel treatment strategies. The SLC16A12 Antibody offers researchers a reliable means to explore the functions and regulatory mechanisms of SLC16A12, paving the way for advancements in metabolic research and drug discovery.
solute carrier family 16, member 12 (monocarboxylic acid, transporter 12);SLC16A12;CJMG;DKFZp686E188;MCT12 ;
UniProt Protein Function:
SLC16A12: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates. Defects in SLC16A12 are a cause of cataract juvenile with microcornea and glucosuria (CJMG). Renal glucosuria is defined by elevated glucose level in the urine without hyperglycemia and without evidence of morphological renal anomalies. Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2.A.1.13) family.Protein type: Transporter, SLC family; Membrane protein, integral; Membrane protein, multi-pass; TransporterChromosomal Location of Human Ortholog: 10q23.31Cellular Component: integral to plasma membraneMolecular Function: creatine transporter activity; lactate transmembrane transporter activity; symporter activityDisease: Cataract, Juvenile, With Microcornea And Glucosuria
UniProt Protein Details:
NCBI Summary:
This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
