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anti-Human CYP11B2 Antibodies:
anti-Mouse (Murine) CYP11B2 Antibodies:
anti-Rat (Rattus) CYP11B2 Antibodies:
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Human Polyclonal CYP11B2 Primary Antibody for WB - ABIN4890921
Brenner, Labreuche, Pico, Scheltens, Poirier, Cambien, Amarenco: The renin-angiotensin-aldosterone system in cerebral small vessel disease. in Journal of neurology 2008
Show all 2 Pubmed References
Horse (Equine) Polyclonal CYP11B2 Primary Antibody for WB - ABIN2776971
Doi, Satoh, Maekawa, Nakamura, Fustin, Tainaka, Hotta, Takahashi, Morimoto, Takase, Ito, Sasano, Okamura: Isoform-specific monoclonal antibodies against 3β-hydroxysteroid dehydrogenase/isomerase family provide markers for subclassification of human primary aldosteronism. in The Journal of clinical endocrinology and metabolism 2014
Human Polyclonal CYP11B2 Primary Antibody for IHC, IHC (p) - ABIN4301715
Scortegagna, Berthon, Settas, Giannakou, Garcia, Li, James, Liddington, Vilches-Moure, Stratakis, Ronai: The E3 ubiquitin ligase Siah1 regulates adrenal gland organization and aldosterone secretion. in JCI insight 1970
Frequencies and distribution of genotype TT of CYP11B2 (C-344T) gene polymorphism among South African Black women, especially those without HIV infection, may prevent them from developing preeclampsia.
Aldosterone-producing adenomas (APAs) exhibit different patterns of CYP11B2 staining that vary from uniform to homogeneous. Approximately 30% of patients with unilateral hyperaldosteronism do not have an APA (show ENPEP Antibodies), but either have an increased number of CYP11B2 expressing micronodules or hyperplasia of the zona glomerulosa. [review]
In conclusion, our meta-analysis indicated that subjects with TT genotype might have higher risk of developing LVH in northern Han Chinese.
study demonstrated significant genetic interaction on Na intake with child obesity by salt-sensitive genes variations, NEDD4L (show NEDD4L Antibodies) and CYP11beta2
The combination of the V386A mutation with the variant CYP11B2 173(Arg) only slightly reduces the 18-hydroxylase and 18-oxidase activity, whereas the V386A mutation with the CYP11B2 173(Lys (show LYZ Antibodies)) variant almost abolishes the 18-hydroxylation and 18-oxidation. In both cases the 11-hydroxylase activity is not affected.
The AG genotype frequency of single nucleotide polymorphism rs542092383 was significantly associated with an increased risk of Essential Hypertension among northern Han Chinese.
the cellular distribution of CYP11B2, CYP11B1 (show CYP11B1 Antibodies), CYP17A1 (show CYP17A1 Antibodies) and KCNJ5 (show KCNJ5 Antibodies) in adrenals from two familial hyperaldosteronism type 3 siblings, was examined.
Aging is associated with a pattern of decreased normal zona glomerulosa CYP11B2 expression.
CYP11B2 methylation was found in patients with aldosterone producing adenomas.
In European continental ancestry patients the C allele (CC or CT) at -344T/C SNP in the aldosterone synthase gene does not significantly influence clinical prognosis of chronic heart failure.
Aldosterone synthase knockout mouse shows odium-induced endothelial sodium channel up-regulation in vascular endothelium
Aldosterone synthase (CYP11B2) is a key regulator of fibrotic remodeling during atrial fibrillation.
Differential regulation of aldosterone synthase and 11beta-hydroxylase transcription by steroidogenic factor-1 (show NR5A1 Antibodies)
Modest increase in aldosterone synthase (AS) expression makes blood pressure more sensitive to salt in mice, suggesting that genetically increased AS expression in humans may contribute to hypertension and cardiovascular complication with high-salt diets.
Fetal adrenal cells in primary culture respond to angiotensin-II (or synthetic ACTH (show POMC Antibodies)) by increasing aldosterone production and aldosterone synthase [P450c18/CYP11B2] activity.
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency.
, aldosterone-synthesizing enzyme
, cytochrome P-450Aldo
, cytochrome P-450C18
, cytochrome P450 11B2, mitochondrial
, cytochrome P450, subfamily XIB (steroid 11-beta-hydroxylase), polypeptide 2
, mitochondrial cytochrome P450, family 11, subfamily B, polypeptide 2
, steroid 11-beta-monooxygenase
, steroid 11-beta/18-hydroxylase
, steroid 18-hydroxylase, aldosterone synthase, P450C18, P450aldo
, cytochrome P450C11
, steroid 11-beta-hydroxylase
, Cytochrome P450 subfamily XIB polypeptide 2 (aldosterone synthase)
, Cytochrome P450, subfamily XIB, polypeptide 2 (aldosterone synthase)
, cytochrome P450 11B3, mitochondrial
, cytochrome P450, subfamily 11B, polypeptide 2
, cytochrome P450-Aldo-1
, cytochrome P450-Aldo-2
, mitochondrial cytochrome P450 11B2
, cytochrome P450, family 11, subfamily B, polypeptide 2