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The product of PNMT catalyzes the last step of the catecholamine biosynthesis pathway, which methylates norepinephrine to form epinephrine (adrenaline). Zusätzlich bieten wir Ihnen PNMT Proteine (14) und PNMT Kits (10) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 94 products:
Human Monoclonal PNMT Primary Antibody für EIA, WB - ABIN954226
Huang, Zhang, Hu, Ma, Yang: Phenylethanolamine N-methyltransferase gene promoter haplotypes and risk of essential hypertension. in American journal of hypertension 2011
Cow (Bovine) Polyclonal PNMT Primary Antibody für IHC (fro), IHC (p) - ABIN115760
Bjartell, Persson, Absood, Sundler, Håkanson: Helodermin-like peptides in noradrenaline cells of adrenal medulla. in Regulatory peptides 1989
Nicotinic stimuli appear to regulate expression of the epinephrine-synthesizing gene PNMT through a previously uncharacterized regulatory element.
PNMT gene is located within human chromosome 17q12 amplicon, including PPP1R1B (zeige PPP1R1B Antikörper), STARD3 (zeige STARD3 Antikörper), TCAP (zeige TCAP Antikörper), PNMT, ERBB2 (zeige ERBB2 Antikörper), MGC14832 and GRB7 (zeige GRB7 Antikörper) genes. PPP1R1B (zeige PPP1R1B Antikörper) ~ ERBB2 (zeige ERBB2 Antikörper) ~ GRB7 (zeige GRB7 Antikörper) locus is amplified in human gastric cancer and breast cancer.
initial velocity studies on human PNMT in the absence and presence of product and dead end (zeige DND1 Antikörper) inhibitors.
The 2-SNP AA haplotype in the PNMT promoter is associated with decreased risk of essential hypertension in Han Chinese.
PNMT G-390A polymorphism is possibly associated with essential hypertension risk in male Chinese Han population.
In Caucasians, phenylethanolamine N-methyltransferase single nucleotide polymorphisms are associated with the development of acute kidney injury, disease severity, and in-hospital mortality.
PNMT variants in cis (zeige CISH Antikörper) may interact with nuclear factors in trans to govern adrenergic activity.
Human PNMT has been crystallized in complex with an inhibitor and the cofactor product S-adenosyl-L-homocysteine and diffraction data measured from a cryocooled crystal extend to a resolution of 2.3 A.
Association between the phenylethanolamine N-methyltransferase gene and multiple sclerosis.
homozygosity/heterozygosity of the phenylethanolamine N-methyltransferase gene polymorphism was highly predictive of significant weight loss with sibutramine during the first 3 months of obesity treatment
genetic variants of PNMT may play a role in the development of essential hypertension.
Presence of local PNMT transcription in human heart after transplantation.
Data suggest that Pnmt plays role in fear response and startle reactivity; compared with wild-type mice, Pnmt-knockout mice exhibit reduced contextual fear but normal cued fear.
Although temperature was normal in Pnmt(-/-) mice, the brown fat response to cold was abnormal with no increase in Ucp-1 (zeige UCP1 Antikörper) or Pgc-1alpha (zeige PPARGC1A Antikörper) mRNA levels (but with an exaggerated cold-induced lipid loss from the tissue).
surprisingly high levels of the epinephrine synthesizing enzyme phenylethanolamine N-methyl transferase (PNMT) were detected in the thymus of young mice.
A truncated mouse phenylethanolamine N-methyltransferase splice variant has dominant-negative activity
PNMT expression is regulated late in mouse gestation by AP2-alpha (zeige TFAP2A Antikörper) and glucocorticoids
clear, significant increase in aggression arising from PNMT overexpression
Regulation of the PNMT gene expression in various compartments of heart includes both corticosterone-dependent and independent mechanisms.
Transcriptional suppression by cAMP as a mechanism for regulating PNMT expression in both normal and neoplastic mouse chromaffin cells.
Neuronal nitric oxide synthase (zeige NOS1 Antikörper) gene inactivation reduces the expression of vasopressin (zeige AVP Antikörper) in the hypothalamic paraventricular nucleus and of PNMT in the adrenal gland of the mouse.
The product of this gene catalyzes the last step of the catecholamine biosynthesis pathway, which methylates norepinephrine to form epinephrine (adrenaline). The enzyme also has beta-carboline 2N-methyltransferase activity. This gene is thought to play a key step in regulating epinephrine production. Alternatively spliced transcript variants have been found for this gene.
, noradrenaline N-methyltransferase
, phenylethanolamine N-methylase