anti-Phosphatidylethanolamine N-Methyltransferase (PEMT) Anticorps

Phosphatidylcholine (PC) is the most abundant mammalian phospholipid. De plus, nous expédions PEMT Kits (9) et PEMT Protéines (4) et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
PEMT 10400 Q9UBM1
PEMT 18618  
PEMT 25511 Q08388
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Top anti-PEMT Anticorps sur

Showing 10 out of 50 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Boeuf (Vache) Lapin Inconjugué WB WB Suggested Anti-PEMT Antibody Titration:  0.2-1 ug/ml  Positive Control:  721_B cell lysate Lanes:   Lane1: 20 ug rat liver lysate  Primary Antibody Dilution:   1:2000  Secondary Antibody:   Anti-rabbit HRP  Secondary Antibody Dilution:   1:15000  Gene Name:   PEMT  Submitted by:   Anonymous 100 μL 2 to 3 Days
Humain Lapin Inconjugué EIA, WB 0.4 mL 6 to 8 Days
Roussette (Chauve-souris) Lapin Inconjugué WB 100 μL 11 to 14 Days
Humain Lapin Inconjugué WB Western blot analysis of PEMT Antibody in T47D cell line lysates (35ug/lane) 400 μL 2 to 3 Days
Humain Lapin Inconjugué WB PEMT antibody used at 1 ug/ml to detect target protein. 50 μg 9 to 11 Days
Humain Lapin Inconjugué WB Western Blot analysis of PEMT expression in transfected 293T cell line by PEMT MaxPab polyclonal antibody.Lane 1: PEMT transfected lysate(25.90 KDa).Lane 2: Non-transfected lysate. 100 μg 11 to 12 Days
Humain Lapin FITC ELISA, WB   200 μL 11 to 14 Days
Humain Lapin Alkaline Phosphatase (AP) ELISA, WB   200 μL 11 to 14 Days
Humain Lapin Biotin ELISA, WB   200 μL 11 to 14 Days
Humain Lapin PE ELISA, WB   200 μL 11 to 14 Days

anti-PEMT Anticorps mieux référencés

  1. Human Polyclonal PEMT Primary Antibody pour ELISA, WB - ABIN543156 : Walkey, Shields, Vance: Identification of three novel cDNAs for human phosphatidylethanolamine N-methyltransferase and localization of the human gene on chromosome 17p11.2. dans Biochimica et biophysica acta 1999 (PubMed)
    Show all 3 Pubmed References

  2. Human Polyclonal PEMT Primary Antibody pour ICC, IF - ABIN4344731 : Wattacheril, Seeley, Angel, Chen, Bowen, Lanciault, Caprioli, Abumrad, Flynn: Differential intrahepatic phospholipid zonation in simple steatosis and nonalcoholic steatohepatitis. dans PLoS ONE 2013 (PubMed)

Plus d’anticorps contre PEMT partenaires d’interaction

Human Phosphatidylethanolamine N-Methyltransferase (PEMT) interaction partners

  1. Our study shows that choline intake in Polish pregnant women is inadequate and that polymorphisms of PEMT rs12325817 and PCYT1A rs7639752 are associated with betaine but not choline concentrations.

  2. PEMT polymorphisms may be associated with the susceptibility to intrauterine fetal death in the Polish population

  3. Study found three gene variants (CLOCK-rs4864548, PEMT-rs936108, and GHRELIN-rs696217) that exhibited uncorrected gene-by-sleep duration interactions in relation to BMI z-scores in a cohort of New Zealand European children. However, no interactions were identified in percentage body fat differences. Notably, these interactions are evident without detectable effects on sleep duration.

  4. In genotypic combination analysis considering PEMT -744GG/CHDH +432GG/BHMT +742GG as the reference combination, PEMT -744GC/CHDH +432GG/BHMT +742GG genotypic combination was significantly higher in mothers of a down syndrome child compared with that in control mothers with an odds ratio of 2.061 (95% CI: 1.10-3.86, P=0.0342).

  5. Results showed that PEMT mRNA expression in liver tissues of non-alcoholic steatohepatitis (NASH) patients was significantly lower than those with simple steatosis suggesting a distinct clinical entity of lean NASH with insufficiency of PEMT activities.

  6. a significant association between the PEMT rs7946 A-allele and a risk of nonalcoholic fatty liver disease, with the effect being more prominent in East-Asians, but not in non-Asians (Meta-Analysis)

  7. Data show that phosphatidylethanolamineN-methyltransferase (PEMT) rs12325817 polymorphism only marginally changed the association value with academic achievement.

  8. Data suggest that maternal dietary intake during lactation (here, choline intake exceeding dietary recommendations) can alter hepatic PEMT activity and increase choline content of breast milk.

  9. MTHFR rs1801131 C allele and PEMT rs4646356 T allele were associated with a high risk of type 2 diabetes in Han Chinese.

  10. The GG genotype of the PEMT G774C polymorphism, higher levels of serum homocysteine and lower levels of serum betaine are associated with an increased risk of microangiopathy in patients with diabetes.

  11. PEMT is a functional single nucleotide polymorphism (rs7946) in PEMT with sporadic Alzheimer's disease risk in a Han Chinese population.

  12. the PEMT -774G>C and CHDH +432G>T polymorphisms were associated with sperm concentration. This finding suggests a possible influence of these genes on sperm quality

  13. genetic association studies on endometriosis in a population of women in Poland: Data suggest interaction between an SNP in PEMT (rs4244593) and an SNP in MTHFR (Ala222Val; rs1801133) in infertile women with some indication of endometriosis.

  14. nvestigation of factors affecting liver PEMT activity: PEMT activity is lower in liver samples from women who are homozygous for an SNP in PEMT (rs12325817)

  15. allele-specific ablation of estrogen receptor-DNA interaction in the PEMT locus prevents hormone-inducible PEMT expression, conferring risk of choline deficiency in women

  16. Choline requirements for both women are increased by the genetic polymorphism rs12325817 in phosphatidylethanolamine-N-methyltransferase.

  17. Total intake of choline and genotype can influence the concentrations of choline and its metabolites in the breast milk and blood of lactating women and thereby affect the amount of choline available to the developing infant.

  18. The allele frequency of PEMT did not show a significant difference between normal control group and fatty liver patients (P=0.222).

  19. an examination of the membrane topography of this enzyme

  20. PEMT2 mRNA expression was inversely related to tumor proliferation and to histologic grade.

Mouse (Murine) Phosphatidylethanolamine N-Methyltransferase (PEMT) interaction partners

  1. fenofibrate partially reversed hepatic steatosis and fibrosis in Pemt(-/-) mice when treatment was initiated after nonalcoholic fatty liver disease (NAFLD) had already been established. Increasing hepatic fatty acid oxidation can compensate for the lower VLDL-triacylglycerol secretion rate and prevent/reverse fatty liver disease in mice lacking PEMT.

  2. Results show that hepatic PEMT protein levels and activity are post-translationally repressed in homocystinuria and correlates with decreased phosphatidylcholine.

  3. Activation of PPARgamma using pioglitazone in high fat diet-fed Pemt(-/-) mice improved liver function, while these mice were still protected against diet-induced obesity and insulin resistance.

  4. Results showed that Pemt deficiency and high-fat diet in mouse model demonstrated the phenotypes resemble to the clinical features of the patients with lean non-alcoholic steatohepatitis.

  5. propose that cold-induced hypothermia in HF-fed Pemt(-/-) mice is linked to plasma hypoglycemia due to compromised hepatic glucose production.

  6. Lack of PEMT in mice does not promote fatty acid oxidation in skeletal muscle.

  7. Decreased lipogenesis in white adipose tissue may contribute to the resistance to diet-induced obesity in Pemt(-/-) mice.

  8. these findings indicate that the inhibition of Pemt activity ameliorates the ER stress associated with diabetic nephropathy in a model of type 1 diabetes

  9. This study evaluated the role of the role of phosphatidylethanolamine N-methyltransferase in hepatic carbohydrate metabolism in chow-fed mice.

  10. Pemt deficiency results in attenuated secretion of very low-density lipoproteins and homocysteine as well as in increased susceptibility to nonalcoholic liver disease.

  11. Lack of phosphatidylethanolamine N-methyltransferase decreased liver damage in Abcb4(-/-) mice caused by exposure of the liver to excess bile acids.

  12. Treatment strategies aimed at inhibition of PEMT might prevent the accumulation of cardiac triacylglycerol that predisposes individuals to compromised cardiac function.

  13. de novo synthesis of choline via PEMT has a previously unappreciated role in regulating whole body energy metabolism.

  14. During differentiation of 3T3-L1 cells to adipocytes, the amount of Sp1 protein decreased by approximately 50% just prior to activation of PEMT.

  15. Dietary docosahexaenoic acid supplementation modulates hippocampal development in the Pemt-/- mouse.

  16. PEMT is required in the secretion of apoB100-containing VLDLs.

  17. Results show that phosphatidylethanolamine N -methyltransferase (PEMT) knockout mice do not display normal concentrations of choline metabolites even with a supplemental source of dietary choline.

  18. Plasma homocysteine is regulated by phospholipid methylation, and is therefore lowered in enzyme-deficient mice.

  19. PEMT activity is involved in many physiologic processes including the flux of lipid between liver and plasma and the delivery of essential fatty acids to blood and peripheral tissues via the liver-derived lipoproteins

  20. This study observed increased numbers of phosphorylated histone H3 positive cells in the Pemt-/- mice (up 54% compared to wild-type mice; p<0.01). We also found decreased calretinin labeling in Pemt-/- (down to 43% compared to wild-type mice; p<0.01).

PEMT profil antigène

Profil protéine

Phosphatidylcholine (PC) is the most abundant mammalian phospholipid. This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. Another distinct synthetic pathway in nucleated cells converts intracellular choline to phosphatidylcholine by a three-step process. The protein isoforms encoded by this gene localize to the endoplasmic reticulum and mitochondria-associated membranes. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms.

Gene names and symbols associated with PEMT

  • phosphatidylethanolamine N-methyltransferase (pemt) anticorps
  • phosphatidylethanolamine N-methyltransferase (MCA3065) anticorps
  • phosphatidylethanolamine N-methyltransferase (pmtA) anticorps
  • phosphatidylethanolamine N-methyltransferase (CNG04250) anticorps
  • phosphatidylethanolamine N-methyltransferase (pemtA) anticorps
  • phosphatidylethanolamine N-methyltransferase (pemtB) anticorps
  • phosphatidylethanolamine N-methyltransferase (PEMT) anticorps
  • phosphatidylethanolamine N-methyltransferase (Pemt) anticorps
  • AI255394 anticorps
  • DDBDRAFT_0204815 anticorps
  • DDBDRAFT_0219474 anticorps
  • DDBDRAFT_0267052 anticorps
  • DDBDRAFT_0267053 anticorps
  • DDB_0204815 anticorps
  • DDB_0219474 anticorps
  • DDB_0267052 anticorps
  • DDB_0267053 anticorps
  • PEAMT anticorps
  • Pempt anticorps
  • Pempt2 anticorps
  • PEMT2 anticorps
  • PHOMETH anticorps
  • PNMT anticorps
  • zgc:55479 anticorps

Protein level used designations for PEMT

phosphatidylethanolamine N-methyltransferase , phospholipid methyltransferase family protein , PEAMT , PEMT2

393127 Danio rerio
3103781 Methylococcus capsulatus str. Bath
3196945 Ruegeria pomeroyi DSS-3
3258746 Cryptococcus neoformans var. neoformans JEC21
8623635 Dictyostelium discoideum AX4
8627247 Dictyostelium discoideum AX4
10400 Homo sapiens
18618 Mus musculus
25511 Rattus norvegicus
360197 Bos taurus
Fournisseurs de qualité sélectionnés pour anti-PEMT (PEMT) Anticorps
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