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CERS2 encodes a protein that has sequence similarity to yeast longevity assurance gene 1. Zusätzlich bieten wir Ihnen Ceramide Synthase 2 Antikörper (63) und Ceramide Synthase 2 Kits (7) und viele weitere Produktgruppen zu diesem Protein an.
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Results show that silencing of ATP6V0C (zeige ATP6V0C Proteine) in highly metastatic prostate cancer (PC) cell lines, inhibited V-ATPase (zeige ATP6V1H Proteine) activity, which coincided with the inhibition of cell migration and invasion in vitro, as well as a marked decrease in the expression of LASS2/TMSG1 probably through positive feedback.
CerS2-knockdown via CRISPR-Cas9 technology in cultured colon epithelial cells impaired barrier function.
Low expression of LASS2 and TGFB1 (zeige TGFB1 Proteine) contributes to the aggressiveness and poor prognosis of hepatocellular carcinoma, and may represent a novel prognostic biomarker for hepatocellular carcinoma patients.
ASGR1 (zeige ASGR1 Proteine) can inhibit the activity of V-ATPase (zeige ATP6V1H Proteine) by interacting with LASS2, thereby suppressing the metastatic potential of hepatoma cells.
Data show that 1-acylglycerol-3-phosphate O-acyltransferase 9 (AGPAT9) inhibit cell growth by regulating expression of KLF4/LASS2/V-ATPase proteins in breast cancer.
these results indicate that miR (zeige MLXIP Proteine)-9 upregulation might be associated with malignant phenotype of bladder cancer. miR (zeige MLXIP Proteine)-9 promotes chemoresistance of bladder cancer cells by target LASS2.
Data show that CERS2 expression was markedly different between various breast cancer cells and inversely correlated with cell invasion.
silencing of TMSG1 increased V-ATPase (zeige ATP6V1H Proteine) activity, decreased extracellular pH and in turn the activation of secreted MMP-2 (zeige MMP2 Proteine), which ultimately promoted metastasis capacity of breast cancer cell.
Results confirmed that TMSG1 is a potential metastasis suppressor gene, and suggested that the mechanism involved the induction of apoptosis and inhibition of cell proliferation via a caspase (zeige CASP3 Proteine)-dependent mitochondrial pathway.
the vacuolar ATPase (V-ATPase) activity and extracellular hydrogen ion concentration were significantly decreased and the activity of secreted matrix metalloproteinase-2 (MMP-2 (zeige MMP2 Proteine)) was downregulated in MCF-7 cells overexpressing LASS2/TMSG1
Deficiency of CerS2 influences intestinal barrier function and the severity of experimental colitis and may represent a potential mechanism for inflammatory bowel disease pathogenesis.
LASS2 plays an important role in efficient liver regeneration in response to partial hepatectomy.
Deletion of CerS2 strongly reduced very long-chain ceramides (Cer24:0, 24:1) but concomitantly increased long-chain ceramides and sphinganine in plasma and colon tissue. In naive CerS2(-/-) mice, the expression of tight junction proteins including ZO-1 (zeige TJP1 Proteine) was almost completely lost in the colon epithelium, leading to increased membrane permeability. Ceramide synthase 2 deficiency aggravates dextran induced colitis in mice.
this study shows that Cers2 limits the levels of S1P (zeige S1PR1 Proteine) in thymus and blood to maintain functional S1P (zeige S1PR1 Proteine) gradients that mediate thymocyte emigration into the circulation
that only LCBs, the substrates common for all of the CerS isoforms, but not ceramides and complex sphingolipids, were restored to the wild-type levels in the Cers2-rescued Cers1 (zeige CERS1 Proteine) mutant mouse brains.
CerS1 (zeige CERS1 Proteine), -2, and -6 are hyperacetylated in the mitochondria of SIRT3 (zeige SIRT3 Proteine)-null mice.
Haploinsufficiency for this enzyme altered the pattern of ceramide acylation in the liver without affecting total ceramide levels, replacing very-long-chain ceramides with long-chain C16-ceramides.
Development of pheochromocytoma in ceramide synthase 2 null mice
our data strongly indicate that G-CSF (zeige CSF3 Proteine)-induced CXCR2 (zeige CXCR2 Proteine) expression is regulated in a CerS2-dependent manner and that CerS2 thereby promotes the migration of neutrophils, thus, contributing to inflammation and the development of EAE and MS.
Data indicate that the augmented rate of death of ceramide synthase 2 (CerS2) null mice is due to elevated levels of tumor necrosis factor alpha (TNFalpha (zeige TNF Proteine)) secretion as a result of enhanced activity of TNFalpha (zeige TNF Proteine)-converting enzyme (TACE (zeige ADAM17 Proteine)).
This gene encodes a protein that has sequence similarity to yeast longevity assurance gene 1. Mutation or overexpression of the related gene in yeast has been shown to alter yeast lifespan. The human protein may play a role in the regulation of cell growth. Alternatively spliced transcript variants encoding the same protein have been described.
LAG1 homolog, ceramide synthase 2
, LAG1 longevity assurance 2
, longevity assurance (LAG1, S. cerevisiae) homolog 2
, tumor metastasis-suppressor gene 1 protein
, LAG1 longevity assurance homolog 2
, TRAM homolog 3
, longevity assurance homolog 2
, translocating chain-associating membrane protein homolog 3