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anti-Mouse (Murine) MIF Antibodies:
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Human Polyclonal MIF Primary Antibody for CyTOF, FACS - ABIN4899419
Chuang, Hung, Tsai, Yeh, Chuang et al.: High concentrations of circulating macrophage migration inhibitory factor in patients with severe blunt trauma: Is serum macrophage migration inhibitory factor concentration a valuable prognostic ... in Critical care medicine 2004
Show all 9 Pubmed References
Human Polyclonal MIF Primary Antibody for FACS, WB - ABIN4899418
Kim, Rongisch, Hager, Grieb, Nourbakhsh, Rennekampff, Bucala, Bernhagen, Pallua: Macrophage Migration Inhibitory Factor in Acute Adipose Tissue Inflammation. in PLoS ONE 2015
Show all 8 Pubmed References
Human Polyclonal MIF Primary Antibody for EIA, ELISA - ABIN250498
Hsieh, Su, Wang, Tsai, Huang, Chang, Lai, Lei, Huang: Hepatitis B virus pre-S2 mutant surface antigen induces degradation of cyclin-dependent kinase inhibitor p27Kip1 through c-Jun activation domain-binding protein 1. in Molecular cancer research : MCR 2007
Show all 3 Pubmed References
Human Monoclonal MIF Primary Antibody for IHC (p), IP - ABIN561823
Goh, Hong, Hong, Lee, Ju, Jeong, Cho, Kim, Lee: eIF3m expression influences the regulation of tumorigenesis-related genes in human colon cancer. in Oncogene 2011
Show all 2 Pubmed References
Human Polyclonal MIF Primary Antibody for ICC, IF - ABIN4334481
Põlajeva, Bergström, Edqvist, Lundequist, Sjösten, Nilsson, Smits, Bergqvist, Pontén, Westermark, Pejler, Forsberg Nilsson, Tchougounova: Glioma-derived macrophage migration inhibitory factor (MIF) promotes mast cell recruitment in a STAT5-dependent manner. in Molecular oncology 2014
Show all 2 Pubmed References
MIF was found to be essential for axis formation and neural development of Xenopus embryos.
Data show that the mif pathway is required for both sensory hair cell (HC) and sensory neuronal cell survival in the ear, for HC differentiation, semicircular canal formation, statoacoustic ganglion (SAG (show SAG Antibodies)) development, and lateral line HC differentiation.
Gene expression of MIF was 30-fold higher in the heart, compared to skeletal muscle and protein expression of MIF was 3-fold higher in the heart compared to skeletal muscle.
renal tubular MIF is an endogenous renoprotective factor in progressive kidney diseases
locally produced MIF in the inflammatory bone lytic site is engaged in the chemoattraction of circulating CXCR4 (show CXCR4 Antibodies)+ osteoclast precursor cells.
MIF expression was induced in chondrocytes of tissue-engineered cartilage, and could exert a profound effect on chondrocytes by promoting cartilage maturation. MIF could also regulate the phenotype of surrounding macrophages, impairing the maturation of transplanted tissues.
loss of autophagy, by pharmacological inhibition or siRNA silencing of Atg5 (show ATG5 Antibodies), enhances MIF secretion by monocytes and macrophages.
CHD7 (show CHD3 Antibodies) is an important factor in the proliferation and stemness maintenance of neural stem/progenitor cells.
MIF-deficient mice have reduced Nippostrongylus brasiliensis burden and mounted an enhanced type 2 immune response, including increased Gata3 (show GATA3 Antibodies) expression and interleukin-13 (show IL13 Antibodies) production in the mesenteric lymph nodes
Sertoli cells to produce MIF under normal conditions. MIFR (show MMP23B Antibodies) is expressed in GFRalpha1 (show GFRA1 Antibodies) and Sertoli cells. MIF induced spermatogonial cell migration
MIF-transgenic cells exhibited substantially decreased levels of p53 (show TP53 Antibodies) after hyperthermia treatment compared with WT and MIF-knockout cells
recombinant macrophage migration inhibitory factor is important for the synthesis of il1beta (show IL1B Antibodies) mRNA in vivo and in isolated macrophages.
The assay monitors the increase in absorbance at 320 nm resulting from keto-to-enol tautomerization of 4-hydroxyphenylpyruvate, a reaction catalyzed by MIF (show AMH Antibodies). We ran a full-diversity screen evaluating the inhibitory activity of 1.6 million compounds.
The rs5844572 polymorphism in MIF (show AMH Antibodies) is linked to the rate of progression and extent of fibrosis in Biliary Atresia Patients, but not with disease susceptibility.
Absolute numbers of MIF (show AMH Antibodies) and IL-1beta (show IL1B Antibodies) mRNA molecules are both accurate and reliable predictors of antidepressant response.
The knockdown of D-DT and MIF (show AMH Antibodies), individually and additively, inhibited the proliferation, migration, and invasion in HeLa and SiHa cells and restrained the growth of xenograft tumor.
No association between coronary artery disease class and -794 CATT5-8 MIF (show AMH Antibodies) polymorphisms with soluble MIF (show AMH Antibodies) levels in CAD (show CAD Antibodies) subjects.
These results have implications for the manner in which D-DT and MIF (show AMH Antibodies) compete with each other for binding to the CD74 (show CD74 Antibodies) receptor and for the relative potency of DRa1-MOG-35-55 and RTL1000 for competitive inhibition of D-DT and MIF (show AMH Antibodies) binding and activation through CD74 (show CD74 Antibodies).
Plasma MIF (show AMH Antibodies) was elevated after cardiac stress (relative to before stress) in patients with a positive stress test, compared with those with a negative stress test. Plasma MIF (show AMH Antibodies) is an early marker for myocardial ischemia. MIF (show AMH Antibodies) was not altered after exercise in peripheral arterial occlusive disease patients, despite the occurrence of claudication, suggesting that plasma MIF (show AMH Antibodies) is not a marker for skeletal muscle ischemia.
Increased serum MIF concentrations have close relation to inflammation, trauma severity and clinical outcomes, substantializing MIF as a good prognostic biomarker after TBI
renal tubular MIF (show AMH Antibodies) is an endogenous renoprotective factor in progressive kidney diseases
MIF (show AMH Antibodies) is primarily an indirect promoter of glioblastoma progression.
plasma MIF concentrations may increase with age in months and parity, but do not change either before and after parturition or before and after postpartum first ovulation in Japanese black cows
Data suggest that, in obese cows, expression of MIF is suppressed in the ampulla and isthmus of Fallopian tubes as compared to normal-weight cows; however, MIF expression is also lower in Fallopian tubes of lean cows. The primary site of MIF expression in Fallopian tube ampulla/isthmus is the tunica mucosa. These studies were conducted in Japanese Black calves.
The objective of the present study was to determine if SNPs in 5' region of bovine MIF affects its promoter activity.
MIF plays a role in early embryo development, and further characterization of MIF expression and its regulation in the endometrium will add significantly to our understanding of early embryo-uterine interactions
The diverse actions of MIF within the immuno-neuroendocrine system may be a result of its occurrence in different isoforms and oligomerization states.
The purification of macrophage migration inhibitory factor (MIF) from bovine brain cytosol and its partial characterization are reported.
Transcription of MIF is induced by activation of PPARgamma2 (show PPARG Antibodies) and inhibited by excessive resistin (show RETN Antibodies).
The high activity of MIF in the maternal and fetal tissues throughout placentation and its expression in the nonpregnant uterus indicate a regulatory role for MIF during embryo receptivity and epitheliochorial placentation
This gene encodes a lymphokine involved in cell-mediated immunity, immunoregulation, and inflammation. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. This lymphokine and the JAB1 protein form a complex in the cytosol near the peripheral plasma membrane, which may indicate an additional role in integrin signaling pathways.
, L-dopachrome tautomerase
, Phenylpyruvate tautomerase
, macrophage migration inhibitory factor
, phenylpyruvate tautomerase
, Macrophage migration inhibitory factor
, delayed early response protein 6
, glycosylation-inhibiting factor
, glutathione-binding 13 kDa protein