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This protein encoded by MPST catalyzes the transfer of a sulfur ion from 3-mercaptopyruvate to cyanide or other thiol compounds. Additionally we are shipping MPST Proteins (13) and MPST Kits (9) and many more products for this protein.
Showing 10 out of 31 products:
Human Polyclonal MPST Primary Antibody for ICC, IF - ABIN4335380
Shibuya, Mikami, Kimura, Nagahara, Kimura: Vascular endothelium expresses 3-mercaptopyruvate sulfurtransferase and produces hydrogen sulfide. in Journal of biochemistry 2009
Show all 3 references for ABIN4335380
Chicken Polyclonal MPST Primary Antibody for WB - ABIN2783349
Lo, Tsai, Tsai, Hua, Tsai, Huang, Tsai, Lai: Identification of over-expressed proteins in oral squamous cell carcinoma (OSCC) patients by clinical proteomic analysis. in Clinica chimica acta; international journal of clinical chemistry 2006
Show all 2 references for ABIN2783349
Human Polyclonal MPST Primary Antibody for FACS, WB - ABIN392001
Akahoshi, Kamata, Kubota, Hishiki, Nagahata, Matsuura, Yamazaki, Yoshida, Yamada, Ishizaki, Suematsu, Kasahara, Ishii: Neutral aminoaciduria in cystathionine ?-synthase-deficient mice; an animal model of homocystinuria. in American journal of physiology. Renal physiology 2014
3-Mercaptopyruvate sulphurtransferase and not cystathionine gamma-lyase (show CTH Antibodies) is the primary regulator of coronary artery hydrogen sulfide (show SQRDL Antibodies) production and function.
In this review, we discuss the roles of non-canonical Hippo/Mst (show MAP3K10 Antibodies) signaling pathways in lymphocyte development and functions. [review]
The crystal structure analysis allows us to propose a detailed mechanism for MST (show MAP3K10 Antibodies) in which an Asp (show ASIP Antibodies)-His-Ser (show SIGLEC1 Antibodies) catalytic triad is positioned to activate the nucleophilic cysteine residue and participate in general acid-base chemistry
In all the investigated cell lines, the activity of MPST was higher than that of CST (show GAL3ST1 Antibodies), which suggests that in these cells, the main pathway of sulfane sulfur formation is the MPST-catalyzed reaction.
Data suggest that impaired rhodanese expression is associated with increased whole cell reactive oxygen species as well as higher mitochondrial superoxide production and predicts mortality in hemodialysis patients.
This work is the first report of a functional genetic polymorphism affecting MPST and should help in investigation of disorders such as mercaptolactate-cysteine disulfiduria.
H2S3 and H2S are produced in the brain by 3-mercaptopyruvate sulfurtransferase.
behavioral abnormality in MST (show MSTO1 Antibodies)-KO mice is caused by MST (show MSTO1 Antibodies) function defects such as an antioxidant insufficiency or a new transducer, H2S (or HS(-)) and/or SOx (show QSOX1 Antibodies) deficiency.
SiRNA silencing of 3-MPST reduced basal bioenergetic parameters and prevented the stimulating effect of 3-MP on mitochondrial bioenergetics.
This protein encoded by this gene catalyzes the transfer of a sulfur ion from 3-mercaptopyruvate to cyanide or other thiol compounds. It may be involved in cysteine degradation and cyanide detoxification. There is confusion in literature between this protein (mercaptopyruvate sulfurtransferase, MPST), which appears to be cytoplasmic, and thiosulfate sulfurtransferase (rhodanese, TST, GeneID:7263), which is a mitochondrial protein. Deficiency in MPST activity has been implicated in a rare inheritable disorder known as mercaptolactate-cysteine disulfiduria (MCDU). Alternatively spliced transcript variants encoding same or different isoforms have been identified for this gene.
thiosulfate sulfurtransferase (rhodanese)
, 3-mercaptopyruvate sulfurtransferase
, mercaptopyruvate sulfurtransferase
, human liver rhodanese
, thiosulfate sulfurtransferase