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The protein encoded by MAOB belongs to the flavin monoamine oxidase family. Additionally we are shipping Monoamine Oxidase B Proteins (17) and Monoamine Oxidase B Kits (15) and many more products for this protein.
Showing 10 out of 94 products:
Chicken Polyclonal Monoamine Oxidase B Primary Antibody for WB - ABIN2781315
Lazrek, Goffard, Schanen, Karquel, Bocket, Lion, Devaux, Hedouin, Gosset, Hober: Detection of hepatitis C virus antibodies and RNA among medicolegal autopsy cases in Northern France. in Diagnostic microbiology and infectious disease 2006
Show all 2 references for ABIN2781315
Human Polyclonal Monoamine Oxidase B Primary Antibody for IHC, IHC (p) - ABIN4892385
Liu, Ren, Liu: Amphetamine manipulates monoamine oxidase-A level and behavior using theranostic aptamers of transcription factors AP-1/NF-kB. in Journal of biomedical science 2016
Human Polyclonal Monoamine Oxidase B Primary Antibody for IHC, IHC (p) - ABIN4335287
Jo, Yarishkin, Hwang, Chun, Park, Woo, Bae, Kim, Lee, Chun, Park, Lee, Hong, Kim, Oh, Park, Lee, Yoon, Kim, Jeong, Shim, Bae, Cho, Kowall, Ryu, Hwang, Kim, Lee: GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease. in Nature medicine 2014
Mouse (Murine) Polyclonal Monoamine Oxidase B Primary Antibody for IHC, WB - ABIN3022152
Bach, Lan, Johnson, Abell, Bembenek, Kwan, Seeburg, Shih: cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties. in Proceedings of the National Academy of Sciences of the United States of America 1988
Human Polyclonal Monoamine Oxidase B Primary Antibody for ELISA, WB - ABIN185506
Domschke, Sheehan, Lowe, Kirley, Mullins, Osullivan, Freitag, Becker, Conroy, Fitzgerald, Gill, Hawi et al.: Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected ... in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005
Cow (Bovine) Polyclonal Monoamine Oxidase B Primary Antibody for IHC, WB - ABIN2781314
Singh, Khan, Shah, Shukla, Khanna, Parmar: Polymorphism in environment responsive genes and association with Parkinson disease. in Molecular and cellular biochemistry 2008
Zebrafish MAO (zMAO) exhibits functional properties similar to human hMAO A as well as exhibits its own unique behavior.
expression, purification & characterization of zebrafish monoamine oxidase (zMAO) using Pichia pastoris expression system is described; zMAO possesses little differential sensitivity to acetylenic inhibitors than exhibited by either human MAO A & MAO (show MAOA Antibodies) B
this study confirm the presence of functionally active MAO in zebrafish brain and other tissues and characterize the neural systems that express MAO and areas of intense activity in the brain.
Monoamine oxidase B levels are highly expressed in gliomas.
The results of this meta-analysis suggest that people in the Asian population with the MAOB intron 13 A allele have an increased risk of Parkinson disease, especially when combined with the COMT (show COMT Antibodies) LL genotype.
Huntington disease (show HTT Antibodies) neural cells exhibit increased Monoamine oxidase-A (show MAOA Antibodies) and Monoamine oxidases-B expression and activity
Report isolation of MOA-B inhibitors from Vernonia cinerea.
These findings demonstrate that regulation of monoamine levels by Mao (show MAO Antibodies) activity in beta cells is pivotal for physiological insulin (show INS Antibodies) secretion and that loss of MaoB expression may contribute to the beta cell dysfunction in type 2 diabetes.
findings indicate that the low activity of monoamine oxidase (show MAO Antibodies) gene polymorphisms has a protective effect on smoking cessation and smoking frequency.
protein environment of MAO-A (show MAOA Antibodies) enhances the polar nucleophilic character of the mechanism compared to that of MAO-B
MAOB A644G polymorphism was associated with Parkinson Disease risk and a subgroup analyses by ethnicity and gender also found significant relationships between this polymorphism and PD risk.
Data (including data from molecular dynamics simulation studies) suggest that the protonation state of the active site residue Lys296 in monoamine oxidase B does not have influence on the hydride transfer reaction in the metabolism of dopamine.
Polymorphisms of COMT (show COMT Antibodies) and MAO-B genes has a unique characteristics among Chinese patients with Parkinson's disease. They may be related with differences in drug response in such patients.
cloning and characterization of monoamine oxidase A (show MAOA Antibodies) and B genes in pig
Activity of monoamine oxidase B in the striatum is reduced during the presymptomatic stage, but returns to the control level during the symptomatic stage of Parkinsonism in mice.
Monoamine oxidase B deficiency (along with monoamine oxidase A (show MAOA Antibodies)) resulted in an array of abnormalities similar to autism-spectrum disorder.
chronic elevations of monoamines, because of the absence of MAO A (show MAOA Antibodies) and MAO B, cause functional alterations that are accompanied with changes in the cellular mechanisms underlying learning and memory.
MAO-B is involved in the acute neurotoxicity of MPTP (show PTPN2 Antibodies) in embryonic and newborn mice
Data suggest that both IR1 (imidazoline receptor 1 (show NISCH Antibodies)) and IR2/Maob play roles in acquisition of behavioral responses in alcoholism; activation of IR1 (show NISCH Antibodies) and IR2/Maob may serve as molecular targets in prevention (and possibly treatment) of alcoholism.
The results of our study further confirms that the dox-inducible astrocytic MAO-B transgenic mouse displays similar age-related behavioral and neuropathological features to other models of Parkinson's disease
MAO-B seems to exert a critical role in the development of postoperative and neuropathic pain
The temporal sequence of events following MAO-B elevation initially involves increased oxidative stress followed by mitochondrial complex I inhibition and finally neurodegeneration.
The protein encoded by this gene belongs to the flavin monoamine oxidase family. It is a enzyme located in the mitochondrial outer membrane. It catalyzes the oxidative deamination of biogenic and xenobiotic amines and plays an important role in the metabolism of neuroactive and vasoactive amines in the central nervous sysytem and peripheral tissues. This protein preferentially degrades benzylamine and phenylethylamine.
amine oxidase [flavin-containing] B
, monoamine oxidase B
, amine oxidase
, amine oxidase [flavin-containing]
, MAO, brain
, MAO, platelet
, adrenalin oxidase
, monoamine oxidase type B
, tyramine oxidase
, monoamine oxidase A
, monoamine oxidase-B