Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Mouse (Murine) Antibodies:
anti-Rat (Rattus) Antibodies:
Go to our pre-filtered search.
Human Polyclonal STS Primary Antibody for ELISA, WB - ABIN559956
Licznerska, Wegman, Nordenskjöld, Wingren: In situ levels of oestrogen producing enzymes and its prognostic significance in postmenopausal breast cancer patients. in Breast cancer research and treatment 2008
Show all 2 references for ABIN559956
Cow (Bovine) Polyclonal STS Primary Antibody for WB - ABIN2776951
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 ABIN2776951
Cow (Bovine) Polyclonal STS Primary Antibody for WB - ABIN2776950
Kríz, Bicíková, Mohapl, Hill, Cerný, Hampl: Steroid sulfatase and sulfuryl transferase activities in human brain tumors. in The Journal of steroid biochemistry and molecular biology 2008
Human Polyclonal STS Primary Antibody for ELISA, WB - ABIN261659
Stowell, Barvian, Young, Bigsby, Verdugo, Bertozzi, Widlanski: A role for sulfation-desulfation in the uptake of bisphenol a into breast tumor cells. in Chemistry & biology 2006
Data show the gene expression profiling of ABC (show ABCB6 Antibodies) transporters in seven tissues.
shows a high sequence identity (60%) to human ABCG2 gene and ABCG2 expression was 6-fold higher than ABCC2 (show ABCC2 Antibodies) and almost 42 fold higher than ABCB1 (show ABCB1 Antibodies), indicating that the ABCG2 probably plays a significant role in the disposition and excretion of xenobiotics
Overexpression of STS in the liver improved metabolic functions in mouse models of obesity and type 2 diabetes through sex-specific mechanisms.
These data suggest that inactivating mutations and functional variants within STS might exert their influence on ADHD vulnerability, and disorder endophenotypes through modulation of the serotonergic system.
steroid sulfatase may influence core and associated ADHD behavioural endophenotypes via both developmental and ongoing mechanisms, and that the 39,X(Y*)O model may represent a useful tool for elucidating the neurobiological basis of these endophenotypes.
analysis of brain pathways mediating the pro-aggressive effect of the steroid sulfatase (Sts) gene
Our data suggest that variation within STS may be particularly associated with the inattentive subtype of ADHD
Collectively, STS point mutations demonstrate restricted localization, causing efficient impairment of the corresponding enzyme activity, and are more unlikely to be responsible for the phenotypic heterogeneity in XLRI subjects
STS expression was not significantly associated with DFS (show FST Antibodies) and OS, despite positive STS expression in 27% of endometrial cancer patients. Therefore, the role of STS as a prognostic factor in patients with endometrial cancer remains unclear and requires further research.
The induced STS facilitates the conversion of inactive estrogen sulfates to active estrogens, which in return attenuates the NF-kappaB (show NFKB1 Antibodies)-mediated inflammation.
The antagonistic actions of glucocorticoids and NFkB on STS expression are similar to the regulation of inflammatory response proteins
Letter/Case Report: novel nonsense mutation in the STS gene in X-linked ichthyosis (show LBR Antibodies).
Data show that both estrogen sulfatase (show ARSH Antibodies) (STS) and estrogen sulfotransferase (EST (show SULT1E1 Antibodies)) were highly expressed in the human umbilical vein endothelial cells (HUVECs).
Effects of steroid hormone on estrogen sulfotransferase (show SULT1E1 Antibodies) and on steroid sulfatase expression in endometriosis tissue and stromal cells
Our analyses show that the two phenotypes in our patient are due to independent genetic defects: a genomic rearrangement involving the Kallmann syndrome 1 gene and a point mutation of the steryl-sulfatase gene.
In both arm and subumbilical skin biopsy of patients with idiopathic hirsutism, there was an up-regulation of STS mRNA expression.
Genetic variation in ARSC may be associated with change in mammographic density after women stop using estrogen-progestin therapy.
These results suggest that the availability of estrogens in the boar epididymis may be locally controlled also by steroid sulphatase and estrogen sulphotransferase.
The protein encoded by this gene catalyzes the conversion of sulfated steroid precursors to estrogens during pregnancy. The encoded protein is found in the endoplasmic reticulum, where it acts as a homodimer. Mutations in this gene are known to cause X-linked ichthyosis (XLI).
steroid sulfatase (microsomal), arylsulfatase C, isozyme S
, breast cancer resistance protein
, arylsulfatase C
, steryl-sulfate sulfohydrolase
, estrone sulfatase
, steroid sulphatase