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anti-Human Stanniocalcin 2 Antibodies:
anti-Mouse (Murine) Stanniocalcin 2 Antibodies:
anti-Rat (Rattus) Stanniocalcin 2 Antibodies:
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Human Monoclonal Stanniocalcin 2 Primary Antibody for ELISA, WB - ABIN563714
Yokobori, Mimori, Ishii, Iwatsuki, Tanaka, Kamohara, Ieta, Kita, Doki, Kuwano, Mori: Clinical significance of stanniocalcin 2 as a prognostic marker in gastric cancer. in Annals of surgical oncology 2010
Show all 4 references for ABIN563714
Human Polyclonal Stanniocalcin 2 Primary Antibody for EIA, IHC (p) - ABIN356935
Ishibashi, Miyamoto, Taketani, Morita, Takeda, Sasaki, Imai: Molecular cloning of a second human stanniocalcin homologue (STC2). in Biochemical and biophysical research communications 1998
Show all 2 references for ABIN356935
Recombinant human and fish STC2 proteins were generated and found to be N-glycosylated homodimers. STC2 is a functional homodimeric glycoprotein, and thecal cell-derived STC2 could play a paracrine role during follicular development. (Stanniocalcin-2)
These findings indicated that STC2 may promote osteoblast differentiation and mineralization by regulating ERK (show EPHB2 Antibodies) activation
STC2 is involved in regulating PAPP-A (show PAPPA Antibodies) activity during the development of atherosclerosis
Data suggest that stanniocalcin 1 (show STC1 Antibodies) and 2 (STC1 (show STC1 Antibodies), STC2) participate in inhibition of proteolytic activity of pregnancy-associated plasma protein-A (PAPP-A (show PAPPA Antibodies)) during folliculogenesis.
Up-regulation of CDK2 and CDK4 and down-regulation of cell cycle inhibitors p16 and p21 were observed after the delivery of STC2. Furthermore, STC2 transduction activated pAKT and pERK 1/2 signal pathways.
The results showed that the expression of HMGA2 and STC2 was positively correlated. Furthermore, STC2 expression was significantly associated with tumor grade and histotype.
This study utilized ER+ IBC to identify a metagene including ABAT (show ABAT Antibodies) and STC2 as predictive biomarkers for endocrine therapy resistance.
STC2 may inhibit epithelial-mesenchymal transition at least partially through the PKC (show PRRT2 Antibodies)/Claudin-1 (show CLDN7 Antibodies)-mediated signaling in human breast cancer cells.
STC2 has a role in promoting cell proliferation and cisplatin resistance in cervical cancer
The aim of this study was to evaluate the clinical value of measuring expression levels of STC2 in colorectal cancer (CRC (show CALR Antibodies)) patients.
Stanniocalcin 2 may contribute to tumor development and radioresistance in cervical cancer.
Stanniocalcin-2 inhibits proteolytic release of IGF and its ability to cause growth retardation upon transgenic overexpression in mice depends on its proteinase inhibitory function.
The Stc2 promoter contains multiple putative xenobiotic response elements.
These results suggest that the up-regulation of STC2 gene expression resulting from abnormal alpha-klotho (show KL Antibodies)-Fgf23 (show FGF23 Antibodies) signaling may contribute to limitation of ectopic calcification.
These results define a novel molecular function for STC2 as a negative modulator of Store-Operated Calcium Entry and provide the first direct evidence for the regulation of Ca2 (show CA2 Antibodies)+ homeostasis by mammalian STC2.
STC2 is linked to PERK signalling in acinar cells and has a role in limiting damage during pancreatic injury.
induced STC2 expression is an essential feature of survival component of the unfolded-protein response
The murine stanniocalcin 2 gene is a negative regulator of postnatal growth.
This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The encoded protein has 10 of its 15 cysteine residues conserved among stanniocalcin family members and is phosphorylated by casein kinase 2 exclusively on its serine residues. Its C-terminus contains a cluster of histidine residues which may interact with metal ions. The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/phosphate homeostasis. Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast cancers.
, STC-related protein
, stanniocalcin-related protein