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Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. Additionally we are shipping ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 Antibodies (36) and many more products for this protein.
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These cases broaden the phenotypic and genetic spectrum of GM3 synthase deficiency due to ST3GAL5 variants. Patients with intellectual disability or furthermore presenting with Rett-like phenotype should be suspected of GM3 synthase deficiency, a disorder of ganglioside biosynthesis.
Data suggest that ganglioside glycosyltransferases ST3GAL5, ST8SIA1 (show ST8SIA1 Proteins), and B4GALNT1 (show B4GALNT1 Proteins) are S-acylated at conserved cysteine residues located close to cytoplasmic border of their transmembrane domains; ST3Gal-II (show ST3GAL2 Proteins) is acylated at conserved cysteine residue in N-terminal cytoplasmic tail; for B4GALNT1 (show B4GALNT1 Proteins) and ST3Gal-II (show ST3GAL2 Proteins), dimer formation controls their S-acylation status.
Studied the miRNA expression in human hepatocellular carcinoma cell lines; 13 differentially expressed miRNAs were identified between MHCC97-H and MHCC97-L cells; and the same results were found in clinical samples. Found that ST3GAL5 was the direct target of miR (show MLXIP Proteins)-26a, miR (show MLXIP Proteins)-548l and miR (show MLXIP Proteins)-34a.
Serum deprivation triggers upregulation of hST3Gal V gene expression through Runx2 activation by BMP signaling in MG-63 cells.
this study indicated that sialylation involved in the development of MDR of AML (show RUNX1 Proteins) cells probably through ST3GAL5 or ST8SIA4 (show ST8SIA4 Proteins) regulating the activity of PI3K (show PIK3CA Proteins)/Akt (show AKT1 Proteins) signaling and the expression of P-gp (show ABCB4 Proteins) and MRP1 (show MDM4 Proteins).
Whole-exome sequencing of patients with salt and pepper syndrome shows a homozygous c.994G>A transition (p.E332K) in the ST3GAL5 gene.
GM3 synthase deficiency, responsible for early-onset epilepsy syndrome, leads to a secondary respiratory chain dysfunction.
Data demonstrate that valproic acid (VPA) transcriptionally regulates human GM3 synthase (hST3Gal V), which catalyzes ganglioside GM3 (show GRM6 Proteins) biosynthesis in ARPE-19 human retinal pigment epithelial cells.
GM3 exhibits the potential to regulate the allosteric structural transition from inactive to a signaling EGFR dimer, by preventing the autophosphorylation of the intracellular kinase domain in response to ligand binding
In vivo expression of the transcript gives rise to two human ST3Gal-V isoforms with distinct characteristics.
These studies establish ganglioside GM3 (show GRM6 Proteins) as a new candidate responsible for neuropathic pain and small fiber neuropathy in diabetes.
Functionally, the repression of St3gal5 suffices to elevate intercellular adhesion and expression of distinct junction-associated proteins, reminiscent of knockdown of Zeb1.
ganglioside GM3 synthase has a role in siRNA-based spherical nucleic acid reversal of impaired wound healing in diabetic mice
Results show that complete and partial deletion of the GM3 synthase gene exert distinct effects on the NP-C (Niemann-Pick disease Type C) phenotype.
genes involved in the sphingolipids metabolism may be modifiers of cystogenesis, and suggest GM3 synthase as a new anti-cystic therapeutic target.
Results suggest that complete, but not partial, inhibition of GM3 (show GRM6 Proteins) synthesis results in robust activation of an alternate pathway that may compensate for the complete absence of the products of GM3 synthase.
the age at death of the npc1 (show NPC1 Proteins)(-/-) mouse can be significantly influenced by many factors, including differences in strain background, other inactivating gene mutations in Siat9 and lxrbeta (show NR1H2 Proteins)
GM3 synthase silencing suppressed lung metastasis in murine breast cancer cells. The molecular mechanism that underlies GM3 synthase mediated migration and invasion was inhibition of the phosphoinositide-3 kinase/Akt (show AKT1 Proteins) pathway.
The defect of hearing ability of GM3 synthase null mice could be attributed to the functional disorganization of the organ of Corti, and the expression of gangliosides, especially GM3 (show GRM6 Proteins), during the maturation of the cochlea.
zST3GalV-2 and mST3GalV are the enzymes responsible for the synthesis of GM4 in zebrafish and mice, respectively.
Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.
, GM3 synthase
, ST3Gal V
, alpha 2,3-sialyltransferase V
, ganglioside GM3 synthase
, lactosylceramide alpha-2,3-sialyltransferase
, sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase; GM3 synthase)
, sialyltransferase 9
, GM3-specific sialytransferase
, mST3Gal V
, sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase)