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The protein encoded by CBS acts as a homotetramer to catalyze the conversion of homocysteine to cystathionine, the first step in the transsulfuration pathway. Zusätzlich bieten wir Ihnen Cystathionine-beta-Synthase Antikörper (138) und Cystathionine-beta-Synthase Proteine (17) und viele weitere Produktgruppen zu diesem Protein an.
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Human CBS ELISA Kit für Sandwich ELISA - ABIN456995
Sun, Sun, Li, Pan, Xie, Wang, Zhang: Potential biomarkers predicting risk of pulmonary hypertension in congenital heart disease: the role of homocysteine and hydrogen sulfide. in Chinese medical journal 2014
Data suggest that impaired cystathionine beta-synthase-hydrogen sulfide (zeige SQRDL ELISA Kits) axis may contribute to the pathogenesis of Parkinson's disease, and that modulation of this axis may become a novel therapeutic approach for Parkinson's disease.
results suggested that reduced cystathionine beta-synthase/hydrogen sulfide (zeige SQRDL ELISA Kits) AMP-activated protein kinase (zeige PRKAA2 ELISA Kits) (CBS-H2S-AMPK (zeige PRKAA1 ELISA Kits)) cascade activity contributed to microglia-mediated neuroinflammation following stroke.
Results indicate that activation of the cystathionine-beta-synthase (CBS) and its product hydrogen sulfide (zeige SQRDL ELISA Kits) (CBS/H2S axis promotes colon carcinogenesis.
showed that N-homocysteinylation of collagen in Cbs(-/-) mice impairs its cross-linking
the findings of this study indicate that a deficiency in 3MST does not significantly affect endotoxemia, while a deficiency in CBS or CSE slightly ameliorates the outcome of LPS-induced endotoxemia in vivo.
These data confirm a key role for the H2S-generating enzymes Cbs and Cth (zeige CTH ELISA Kits) in pulmonary vascular development and homeostasis and in lung alveolarization.
genetic deficiency results in reduced Tet1 and Tet2 (zeige TET2 ELISA Kits) expression, which leads to hypermethylation of Foxp3 (zeige FOXP3 ELISA Kits), and impairment of Treg cell differentiation and immune homeostasis.
Elevated homocytsteine levels in the CBS-/+ mouse skeletal muscles caused diminished anti-oxidant capacity and contributed to enhanced total protein as well as PGC-1alpha (zeige PPARGC1A ELISA Kits) specific nitrotyrosylation after ischemia.
CBS disruption causes embryo retention and developmental delay in the mouse oviduct.
CBS is present in adrenocortical cells and accounts for H2S generation in adrenal glands. CBS is critical for maintenance of mitochondrial function and glucocorticoid production in adrenal cortex.
CBS sequencing resulted in the identification of two novel mutations, a missense change (c.467T>C; p.Leu156Pro) in exon 7 and an in-frame deletion (c.808_810del; p.Glu270del) in exon 10. In addition, a recurrent missense mutation (c.770C>T; p.Thr257Met) in exon 10 of the gene was also identified.
Nitration-mediated deficiency of cystathionine beta-synthase activity accelerates the progression of hyperhomocysteinemia.
Abundant expression of CBS, localized in renal tubular epithelial cells, was revealed in human and rat renal tissue, which correlated negatively with the progression of fibrotic disease.
c.797 G>A (p.R266K) cystathionine beta-synthase mutation has a role in causing homocystinuria by affecting protein stability
The current study observed significant differences in the frequency of the CBS 844ins68 allele across populations. There is a significant association between CBS c.844ins68 polymorphism and cleft lip and palate in the Indian population.
Cystathionine beta-synthase and PGRMC1 (zeige PGRMC1 ELISA Kits) function as carbon monoxide sensors in health and disease. (Review)
These findings may contribute to highlight that the MTHFR (zeige MTHFR ELISA Kits) and CBS polymorphisms involvement in sickle cell anemia (SCA)pathophysiology is likely to be far more complex than it was explored to date
Uterine artery hydrogen sulfide (zeige SQRDL ELISA Kits) production is augmented with endothelium and smooth muscle CBS upregulation, contributing to uterine artery vasodilation in the estrogen-dominant physiological states in the proliferative phase of the menstrual cycle and pregnancy.
Common polymorphisms in MTHFR (zeige MTHFR ELISA Kits), methionine synthase (zeige MTR ELISA Kits) and cystathione beta lyase genes have no role in premature acute myocardial infarction in Pakistani population.
These findings indicate that greater synthesis of phosphatidylcholine (zeige SGMS1 ELISA Kits) and antioxidants contribute to the better performance and immuno-metabolic status in methionine-supplemented cows.
The protein encoded by this gene acts as a homotetramer to catalyze the conversion of homocysteine to cystathionine, the first step in the transsulfuration pathway. The encoded protein is allosterically activated by adenosyl-methionine and uses pyridoxal phosphate as a cofactor. Defects in this gene can cause cystathionine beta-synthase deficiency (CBSD), which can lead to homocystinuria. Multiple alternatively spliced transcript variants have been found for this gene.
, cystathionine beta-synthase
, cystathionine beta-synthase CBS
, hemoprotein H-450
, serine sulfhydrase
, methylcysteine synthase