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RAET1E belong to the RAET1 family, which consists of major histocompatibility complex (MHC) class I-related genes located in a cluster on chromosome 6q24.2-q25.3. Additionally we are shipping Retinoic Acid Early Transcript 1E Antibodies (117) and Retinoic Acid Early Transcript 1E Proteins (10) and many more products for this protein.
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decreased expression levels of ULBP4 in NPC (show NPC1 ELISA Kits) tissues as compared to that in normal NP epithelial tissues. In addition, low ULBP4 expression correlated with poor OS, DFS (show FST ELISA Kits), DMFS, and may prove to be a novel prognostic factor.
Blocking the interaction of NKG2D (show KLRK1 ELISA Kits) with its ligands deleted the sensitizing effects of HCQ. In addition, we showed that HCQ did not affect the synthesis or degradation of ULBP4, but induced the translocation of ULBP4 from the cytoplasm to the cell membrane
5 of the 7 promoter polymorphisms of the RAET1E gene may disrupt transcription factor binding
RAET1E promoter polymorphism has increased to nine types, and there are now 12 alleles determined by the coding exons, including one null.
Patients whose tumors had high expression of RAET1E, ULBP1 (show ULBP1 ELISA Kits) and ULBP3 (show ULBP3 ELISA Kits) surviving a median of 11, 14 and 11 months, respectively, compared with disease-specific survival of 29, 30 and 25 months in patients whose tumors showed no expression of these ligands
Binds the activating receptor NKG2D (show KLRK1 ELISA Kits).
immune escape mechanism of tumors via alternative splicing of ULBP RNA to generate a free soluble ULBP protein, RAET1E2, that may impair NKG2D (show KLRK1 ELISA Kits)-mediated NK cell cytotoxicity to tumors
All ULBP4 splice variants (ULBP4-I, ULBP4-II and ULBP4-III) were type 1 membrane-spanning molecules and had the ability to bind with human NKG2D (show KLRK1 ELISA Kits) receptor in vitro
data suggest that ULBP4 functions as a ligand for both TCRgammadelta and NKG2D (show KLRK1 ELISA Kits) and may play a key role in immune surveillance of tumor development and clearance of viral infection
Study reports that retinoic acid early induced transcript-1-d and retinoic acid early induced transcript-1-e (Raet1) genes are induced early upon experimental autoimmune encephalomyelitis onset and reach a maximal expression at the peak of the pathology. Study also shows that macrophages as well as microglia, are cellular sources of Raet1 transcripts.
CD4 (show CD4 ELISA Kits)(+) NKG2D (show KLRK1 ELISA Kits)(+) T cells induce NKG2D (show KLRK1 ELISA Kits) down-regulation in natural killer cells in CD86 (show CD86 ELISA Kits)-RAE-1epsilon transgenic mice.
Reveal Raet1e, a major histocompatibility complex class 1-like molecule expressed in lesional aortic endothelial cells and macrophage-rich regions, as a novel atherosclerosis gene.
Raet1e genes are directly transcriptionally activated by E2F (show E2F1 ELISA Kits) family transcription factors, which play a central role in regulating cell cycle entry.
RAE1 expression was sufficient to induce the recruitment of adoptively transferred CTLs to islets.
This gene belong to the RAET1 family, which consists of major histocompatibility complex (MHC) class I-related genes located in a cluster on chromosome 6q24.2-q25.3. This and RAET1G protein differ from other RAET1 proteins in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. This protein functions as a ligand for NKG2D receptor, which is expressed on the surface of several types of immune cells, and is involved in innate and adaptive immune responses. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
NKG2D ligand 4
, RAE-1-like transcript 4
, lymphocyte effector toxicity activation ligand
, Rae-1 epsilon
, retinoic acid early-inducible protein 1-epsilon