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CERS2 encodes a protein that has sequence similarity to yeast longevity assurance gene 1. 再加上，我们可以发Ceramide Synthase 2 蛋白 (5) 和 Ceramide Synthase 2 试剂盒 (2)和数多这个蛋白质的别的产品。
Showing 10 out of 53 products:
Human Monoclonal CERS2 Primary Antibody for ELISA, WB - ABIN526190
Separovic, Breen, Joseph, Bielawski, Pierce, VAN Buren, Gudz: Ceramide synthase 6 knockdown suppresses apoptosis after photodynamic therapy in human head and neck squamous carcinoma cells. in Anticancer research 2012
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Human Polyclonal CERS2 Primary Antibody for WB - ABIN265218
Becker, Wang-Eckhardt, Yaghootfam, Gieselmann, Eckhardt: Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2. in Histochemistry and cell biology 2008
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Cow (Bovine) Polyclonal CERS2 Primary Antibody for WB - ABIN2781175
Laviad, Albee, Pankova-Kholmyansky, Epstein, Park, Merrill, Futerman: Characterization of ceramide synthase 2: tissue distribution, substrate specificity, and inhibition by sphingosine 1-phosphate. in The Journal of biological chemistry 2008
Human Polyclonal CERS2 Primary Antibody for WB - ABIN526188
Jensen, Calvert, Volpert, Kouri, Hurley, Luciano, Wu, Chalastanis, Futerman, Stegh: Bcl2L13 is a ceramide synthase inhibitor in glioblastoma. in Proceedings of the National Academy of Sciences of the United States of America 2014
Data show that 1-acylglycerol-3-phosphate O-acyltransferase 9 (AGPAT9 (显示 AGPAT9 抗体)) inhibit cell growth by regulating expression of KLF4 (显示 KLF4 抗体)/LASS2/V-ATPase (显示 ATP6V1H 抗体) proteins in breast cancer.
these results indicate that miR (显示 MLXIP 抗体)-9 upregulation might be associated with malignant phenotype of bladder cancer. miR (显示 MLXIP 抗体)-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 (显示 ATP6V1H 抗体) activity, decreased extracellular pH and in turn the activation of secreted MMP-2 (显示 MMP2 抗体), 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 (显示 CASP3 抗体)-dependent mitochondrial pathway.
the vacuolar ATPase (V-ATPase (显示 DNAH8 抗体)) activity and extracellular hydrogen ion concentration were significantly decreased and the activity of secreted matrix metalloproteinase-2 (MMP-2 (显示 MMP2 抗体)) was downregulated in MCF-7 cells overexpressing LASS2/TMSG1
the inhibitory effect of the LASS2 on growth, invasion and metastasis of prostate cancer cells
Co-expression of CerS2 with CerS4 (显示 CERS4 抗体)/CerS6 (显示 CERS6 抗体) reversed the inhibitory effect of long chain ceramides on cell proliferation and the induction of apoptosis. we detected no effect on cell proliferation.
expression and role of ceramide synthase-2 in the lung
results contribute to the conclusion that LASS2/TMSG1 could regulate V-ATPase (显示 ATP6V1H 抗体) activity and intracellular pH through the direct interaction of its homeodomain and the C subunit of V-ATPase (显示 ATP6V1H 抗体)
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 (显示 CERS1 抗体) mutant mouse brains.
CerS1 (显示 CERS1 抗体), -2, and -6 are hyperacetylated in the mitochondria of SIRT3 (显示 SIRT3 抗体)-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 (显示 CSF3 抗体)-induced CXCR2 (显示 CXCR2 抗体) 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 (显示 TNF 抗体)) secretion as a result of enhanced activity of TNFalpha (显示 TNF 抗体)-converting enzyme (TACE (显示 ADAM17 抗体)).
CerS2-deficient kidneys were completely depleted of phytosphingosine-containing cortical sulfatides without any compensatio
we first report that Lass2 deficiency caused the downregulation of miR (显示 MLXIP 抗体)-694 and the upregulation of its target gene Tnfaip3 (显示 TNFAIP3 抗体) in vivo in mice, which may be related to a high risk of occurrence of hepatocellular carcinoma
The identification of specific cell types in which CerS2 protein is expressed is prerequisite to further mechanistic characterization of phenotypic abnormalities exhibited by CerS2-deficient mice.
Lass2 is a protective gene against diethylnitrosamine-induced liver tumorigenesis; and upregulation of the TGF-beta1 (显示 TGFB1 抗体)-Smad4 (显示 SMAD4 抗体)-PAI-1 (显示 SERPINE1 抗体) axis may contribute to the vulnerability of Lass2-knockout mice to diethylnitrosamine.
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