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LECT2 encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth of chondrocytes and osteoblasts. Additionally we are shipping LECT2 Kits (19) and LECT2 Proteins (10) and many more products for this protein.
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Circulating LECT2 concentrations were increased in individuals with NAFLD (show TSC2 Antibodies) and those with MetS (show ETV3 Antibodies), but not in those with atherosclerosis. The relationship between LECT2 and both NAFLD (show TSC2 Antibodies) and MetS (show ETV3 Antibodies) might be mediated by its association with abdominal obesity and lipid metabolism.
VFA was the strongest predictor of plasma LECT2 that is a potential biomarker linking visceral obesity to dyslipidemia
LECT2 was found to be catalytically inactive as a metalloendopeptidase (show THOP1 Antibodies) against various types of peptide sequences, including pentaglycine.
the tissue levels of THBS2 (show THBS2 Antibodies) and LECT-2 may correlate with the stage of atherosclerosis.
findings indicated that serum LECT2 level is negatively associated with the presence of diabetic retinopathy and suggest that low circulating LECT2 level is a risk factor for diabetic retinopathy
LECT2 amyloidosis is prevalent among Hispanic decedents in New Mexico.
Localized LECT2 amyloidosis of the adrenal gland with coexisting MGUS: a diagnostic challenge.
LECT2 immunostain is useful in confirming subtype of amyloid within the liver in ALECT2..
There were no mutations detected in the LECT2 gene, although all renal leukocyte chemotactic factor 2 amyloidosis patients tested were homozygous for the G nucleotide in a non-synonymous SNP at position 172.
LECT2 is regulated by beta-catenin (show CTNNB1 Antibodies) in HCC (show FAM126A Antibodies) in both mice and men, but serum LECT2 reflects beta-catenin (show CTNNB1 Antibodies) activity only in mice. Serum LECT2 could be a potential biomarker of HCC (show FAM126A Antibodies) in patients.
This study demonstrates the rapid response of LECT2 preceding body weight alterations during weight cycling in mice.
We found that treatment with LECT2 enhanced H. pylori killing and nitric oxide production in macrophages. In addition, DNA-binding activity and nuclear translocation of p65 (show NFkBP65 Antibodies) were up-regulated by LECT2 treatment
LECT2 improves protective immunity in bacterial sepsis, possibly as a result of enhanced macrophages functions via the CD209a receptor.
Zinc stabilizes the LECT2 structure.
Data suggest the involvement of LECT2 in the regulation of fatal SEA (show Slc25a1 Antibodies)-induced toxicity in d-GalN (show GAL Antibodies)-sensitized mice.
Our results suggest that LECT2 regulates neuritic extension through microtubular morphallaxis through the control of katanin-P60 (show STIP1 Antibodies) levels.
Our results show that LECT2 regulates the extension of axons and dendrites and the expressions of NGF (show NGFB Antibodies), BDNF (show BDNF Antibodies) and NT-3 (show NTF3 Antibodies) during neuronal development.
LECT2, which encodes a protein with chemotactic properties for human neutrophils, is a direct target gene of Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling in the liver.
LECT2 directly suppresses the development of collagen antibody induced arthritis
This gene encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth of chondrocytes and osteoblasts. This protein has high sequence similarity to the chondromodulin repeat regions of the chicken myb-induced myeloid 1 protein. A polymorphism in this gene may be associated with rheumatoid arthritis.
, leukocyte cell-derived chemotaxin-2
, chondromodulin II
, cell-derived chemotaxin 2
, myeloid protein (mim-1)
, myeloid protein 1