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Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. Zusätzlich bieten wir Ihnen Glutathione S-Transferase mu 3 (Brain) Antikörper (46) und Glutathione S-Transferase mu 3 (Brain) Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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Human glutathione S-transferase mu 3 (brain) ELISA Kit für Sandwich ELISA - ABIN417504
Singh, Prasad, Singh, Singh, Gupta, Paliwal, Pandey, Gupta: Human Glutathione S-Transferase Enzyme Gene Polymorphisms and Their Association With Neurocysticercosis. in Molecular neurobiology 2016
The individuals carrying the deletions of GSTM1 (zeige GSTM1 ELISA Kits) and GSTT1 (zeige GSTT1 ELISA Kits) were at risk for Neurocysticercosis (NCC (zeige SLC12A3 ELISA Kits)). Genetic variants of GSTM3 and GSTP1 (zeige GSTP1 ELISA Kits) were not associated with NCC (zeige SLC12A3 ELISA Kits).
Expression of GSTM3 might be regulated by epigenetic changes in lens tissue. Hypermethylation in GSTM3 promoter and altered histone modification might have a role in the ARC (zeige NOL3 ELISA Kits) formation.
This meta-analysis suggested that the GSTT1 (zeige GSTT1 ELISA Kits) and GSTM3 polymorphisms might influence osteosarcoma risk.
No associations between the GSTT1, GSTP1, and GSTM3 genotypes and neoplasia risk were observed. In conclusion, we determined the genotype distribution of GST polymorphisms in control subjects and breast cancer patients from northeastern Mexico.
NSD1 (zeige NSD1 ELISA Kits) interacted with RNAPII and bound to GSTM3 -63A/C TATA box.
To identify the genotypes of CYP1A1 (zeige CYP1A1 ELISA Kits), GSTM1 (zeige GSTM1 ELISA Kits), GSTM3, GSTT1 (zeige GSTT1 ELISA Kits) and GSTP1 (zeige GSTP1 ELISA Kits) in a case-control study.
All three markers correlated significantly with regional lymph node metastasis: FXYD3 (zeige FXYD3 ELISA Kits) (p = 0.0110), S100A11 (zeige S100A11 ELISA Kits) (p = 0.0071), and GSTM3 (p = 0.0173) in colon cancer lymphatic metastasis.
This meta-analysis suggests that the GSTM3 A/B polymorphism may be an important protective factor for head and neck cancer, especially of laryngeal cancer and Caucasian populations.
rs1332018 genetic variants in the GSTM3 promoter predispose the host to downregulating GSTM3 expression in kidney, facilitate carcinogenesis, and predict an unfavourable postoperative prognosis of renal cell carcinoma.
In conclusion, this epistatic interaction showed a high degree of consistency when stratifying by sex, the epsilon4 allele of apolipoprotein E (zeige APOE ELISA Kits) genotype, and geographic region.
Six proteins were regulated at both basal and inducible levels exhibiting the largest dynamic range of Nrf2 (zeige NFE2L2 ELISA Kits) regulation: cytochrome CYP2A5, GSTM3, GSTM1 (zeige GSTM1 ELISA Kits), ENTPD5 (zeige ENTPD5 ELISA Kits),UDPGDH (zeige UGDH ELISA Kits), and EPHX1 (zeige EPHX1 ELISA Kits).
Data show that beta-catenin (zeige CTNNB1 ELISA Kits) accumulation increases GST activity in nuclei of HCC (zeige FAM126A ELISA Kits) cells, and suggest that GSTM3 may be a novel target gene of the beta-catenin (zeige CTNNB1 ELISA Kits)/Tcf (zeige HNF4A ELISA Kits)-Lef complex.
Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants.
glutathione S-transferase M3 (brain)
, glutathione S-transferase M3
, glutathione S-transferase M4
, glutathione S-transferase Mu 3
, glutathione S-transferase Yb4
, GST class-mu 3
, S-(hydroxyalkyl)glutathione lyase M3
, brain GST
, brain type mu-glutathione S-transferase
, glutathione S-alkyltransferase M3
, glutathione S-aralkyltransferase M3
, glutathione S-aryltransferase M3
, glutathione S-transferase, Mu-3
, glutathione S-transferase mu 3
, glutathione-S-transferase, mu
, glutathione S-transferase GT9.3