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Human Resistin Protein expressed in Escherichia coli (E. coli) - ABIN413761
Shen, Zhang, Gan, Wang, Wang, LeMaire, Coselli, Wang et al.: Up-regulation of PTEN (phosphatase and tensin homolog deleted on chromosome ten) mediates p38 MAPK stress signal-induced inhibition of insulin signaling. A cross-talk between stress signaling and ... in The Journal of biological chemistry 2006
Show all 2 Pubmed References
Human Resistin Protein expressed in HEK-293 Cells - ABIN2730725
Nakayama, Aoki, Uchihashi, Nishijima-Matsunobu, Yamamoto, Kakihara, Iwakiri, Fujimoto, Toda: Interaction between Esophageal Squamous Cell Carcinoma and Adipose Tissue in Vitro. in The American journal of pathology 2016
Mouse (Murine) Resistin Protein expressed in HEK-293 Cells - ABIN1344359
Daquinag, Zhang, Amaya-Manzanares, Simmons, Kolonin: An isoform of decorin is a resistin receptor on the surface of adipose progenitor cells. in Cell stem cell 2011
The effects of exogenous human kisspeptin-10 (KP10) were studied on three important adipokines, namely, adiponectin (show ADIPOQ Proteins), leptin (show LEP Proteins), and resistin in a set of four chair-restraint habituated intact adult male rhesus monkeys.
Results show that resistin down-regulates the transcription of GLUT1 (show SLC2A1 Proteins) by suppressing the expression of PPARG (show PPARG Proteins), thus causing impaired glucose transportation in endothelial cell layers.
Serum resistin level is a biomarker for aortic stiffness in patients with coronary artery disease.
The RETN-420 C>G polymorphism may be related to obesity with G allele as a risk factor (Meta-Analysis)
In women, elevated levels of serum resistin are significantly associated with higher rates of incident atrial fibrillation and partially mediate the association between BMI and AF.
Resistin gene expression levels were significantly higher in receptor negative subtypes, especially estrogen receptor (show ESR1 Proteins) negative cases in African American (AA) women. Resistin may serve as an early breast cancer biomarker and possible therapeutic target for AA breast cancer.
serum and lung adiponectin (show ADIPOQ Proteins), leptin (show LEP Proteins), and resistin were measured in an atopic adult study population following exposure to allergen and diesel exhaust
Serum resistin levels are elevated in psoriatic arthritis but do not correlate with disease activity.
Low chemerin (show RARRES2 Proteins) and high resistin levels were associated with carotid disease severity, suggesting that these adipokines may act as potential markers for plaque instability and stroke risk.
Plasma resistin was inversely associated with the extent of methylation at SNP-420 mainly dependent on the SNP-420 genotype. Body mass index was positively associated with methylation at SNP-420 in the C/C genotype.
This study elucidates the detailed mechanism of low shear stress regulating the resistin-induced catabolic COX-2 expression.
Resistin may enhance inflammation by cross-talking with TLR4 (show TLR4 Proteins)/NF-kappaB (show NFKB1 Proteins) signaling during the development of coronary arteritis in mice
OLI (show TOMM22 Proteins) is a physiological repressor of systemic resistin release whereas FFA upregulate resistin release in vitro from adipocytes.
Resistin possibly acts via an intracrine pathway as an intracellular sensor, regulating the adipocyte insulin (show INS Proteins) sensitivity.
In 3T3-L1 adipocytes, catechin and quercetin attenuated TNF-alpha (show TNF PLURAL_@37961@)-induced elevated protein carbonyls, increased proinflammatory cytokine expression (MCP-1 (show CPT1B PLURAL_@37961@), resistin), and decreased adiponectin (show ADIPOQ PLURAL_@37961@).
Mouse Resistin has regulative effects on murine bone marrow hematopoiesis.
murine resistin is increased in the lungs of wild-type mice following acute ozone exposure but does not promote ozone-induced lung pathology.
Inhibition of miR (show MLXIP Proteins)-696 restored the triglycerides content by up to 80%, which suggests that, in C2C12 cells, resistin at least partially increases the deposition of lipids through miR (show MLXIP Proteins)-696.
Resistin regulates PAI-1 (show SERPINE1 Proteins) expression in 3T3-L1 adipocytes via Akt (show AKT1 Proteins) phosphorylation.
Oxidized-LDL promotes the expression and secretion of visfatin (show NAMPT Proteins) and resistin through its activation of endoplasmic reticulum stress.
ET type-A receptor, ERK1/2, JNKs, AKT (show AKT1 Proteins), and JAK2 (show JAK2 Proteins), but not ET type-B receptor or p38 (show CRK Proteins), are necessary for the ET-1 (show EDN1 Proteins) stimulation of resistin gene expression
The data suggest that there is local cooperation between resistin and PPARgamma (show PPARG Proteins) expression in the porcine ovary. Resistin significantly increased the expression of PPARgamma (show PPARG Proteins), whereas PPARgamma (show PPARG Proteins) decreased resistin expression; thus, PPARgamma (show PPARG Proteins) is a new key regulator of resistin expression and function.
The expression, immunolocalization and concentration of resistin in different sized ovarian follicles, was investigated.
This gene belongs to the family defined by the mouse resistin-like genes. The characteristic feature of this family is the C-terminal stretch of 10 cys residues with identical spacing. The mouse homolog of this protein is secreted by adipocytes, and may be the hormone potentially linking obesity to type II diabetes. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
, C/EBP-epsilon regulated myeloid-specific secreted cysteine-rich protein precursor 1
, adipose tissue-specific secretory factor
, c/EBP-epsilon-regulated myeloid-specific secreted cysteine-rich protein
, cysteine-rich secreted protein A12-alpha-like 2
, cysteine-rich secreted protein FIZZ3
, found in inflammatory zone 3
, resistin delta2
, adipose-specific cysteine-rich secreted protein A12-alpha
, dominant inhibitory adipocyte-specific secretory factor
, adipocyte specific secreted hormone