|Other Names||Antigen-presenting glycoprotein CD1d, R3G1, CD1d, CD1D|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.|
|Precautions||This product is for research use only. Not for use in diagnostic or therapeutic procedures.|
|Function||Antigen-presenting protein that binds self and non-self glycolipids and presents them to T-cell receptors on natural killer T-cells.|
|Cellular Location||Cell membrane; Single- pass type I membrane protein Basolateral cell membrane; Single- pass type I membrane protein Endosome membrane; Single-pass type I membrane protein. Lysosome membrane; Single- pass type I membrane protein Endoplasmic reticulum membrane; Single-pass type I membrane protein Note=Subject to intracellular trafficking between the cell membrane, endosomes and lysosomes.|
|Tissue Location||Expressed on cortical thymocytes, on certain T-cell leukemias, and in various other tissues|
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Provided below are standard protocols that you may find useful for product applications.
This gene encodes a divergent member of the CD1 family oftransmembrane glycoproteins, which are structurally related to themajor histocompatibility complex (MHC) proteins and formheterodimers with beta-2-microglobulin. The CD1 proteins mediatethe presentation of primarily lipid and glycolipid antigens of selfor microbial origin to T cells. The human genome contains five CD1family genes organized in a cluster on chromosome 1. The CD1 familymembers are thought to differ in their cellular localization andspecificity for particular lipid ligands. The protein encoded bythis gene localizes to late endosomes and lysosomes via atyrosine-based motif in the cytoplasmic tail.
Miura, S., et al. J. Virol. 84(22):11614-11623(2010)Moll, M., et al. Blood 116(11):1876-1884(2010)Liu, J., et al. J. Immunol. 184(9):4973-4981(2010)Davila, S., et al. Genes Immun. 11(3):232-238(2010)Brandl, C., et al. PLoS ONE 5 (5), E10800 (2010) :
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