Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The protein encoded by CD163 is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. Additionally we are shipping CD163 Antibodies (420) and CD163 Kits (58) and many more products for this protein.
Showing 10 out of 17 products:
In diabetic mice, increased sCD163 at wk 5 and decreased percentage of CD163(+) monocytes at wk 10 preceded alteration in kidney collagen IV mRNA at wk 20. In vitro incubation of monocytes in anti-inflammatory glucocorticoid increased the percentage of CD163(+) monocytes.
During ischaemia, soluble CD163 functions as a decoy receptor for TWEAK (show TNFSF12 Proteins), to regulate TWEAK (show TNFSF12 Proteins)-induced activation of canonical nuclear factor-kappaB and Notch (show NOTCH1 Proteins) signalling necessary for myogenic progenitor cell proliferation.
Data indicate an essential substrate motif for ADAM17 (show ADAM17 Proteins)-mediated CD163 and proTNF-alpha cleavage in macrophages.
alpha(1)-Acid glycoprotein (show ORM1 Proteins) up-regulates CD163 via TLR4 (show TLR4 Proteins)/CD14 protein (show ERGIC2 Proteins) pathway: possible protection against hemolysis-induced oxidative stress.
Data show that telmisartan reduced the mRNA expression of CD11c (show ITGAX Proteins) and TNF-alpha (show TNF Proteins), M1 macrophage markers, and significantly increased the expressions of M2 markers, such as CD163, CD209 (show CD209 Proteins).
Assignment of the CD163 antigen to mouse chromosome 6 band F2.
Most cases of histiocytic sarcoma expressed histiocytic markers CD68 (show CD68 Proteins) (6 of 7 cases), CD163 (5 of 5 cases), and PU.1 (3 of 4 cases).
Within a diabetic cohort, the percentage of monocytes expressing CD163 was decreased in those subjects with complications, compared to those without complications. These changes were not accompanied by a change in gene expression. Glucocorticoids increased CD163 expression in cultured peripheral blood monocytes from non-diabetic persons.
sCD163 was markedly elevated in autoimmune hepatitis (AIH) in the acute phase, normalised by successful treatment in complete responders, but remained higher in the incompletely responding cases. Our results demonstrate macrophage activation in AIH paralleling disease activity, severity and treatment response, suggesting a role for macrophage activation in AIH.
High CD163 expression is associated with glomerular inflammation in lupus nephritis.
analysis of plasma CXCL10 (show CXCL10 Proteins), sCD163 and sCD14 in virological suppression and risk of cardiovascular disease
we found that higher percentages of circulating CD14 (show NDUFA2 Proteins)+CD204+, CD14 (show NDUFA2 Proteins)+CD163+CD204+ M2-like monocytes were significantly associated with TNM (show ODZ1 Proteins) stage, lymph node metastasis, and histological differentiation.
CD163 expression is significantly upregulated in human masticatory mucosa during wound healing
Soluble CD163, which is identified as a marker of inflammation and type II diabetes, is elevated in polycystic ovary syndrome.
soluble CD163 modulates the immune response to Dermatophagoides pteronyssinus allergens potentiating anti-inflammatory, homeostatic mechanisms.
The mean serum-soluble CD163 level was higher in the ANCA-associated renal vasculitis patients with infectious complications than in the active-vasculitis patients, inactive-vasculitis patients, and normal controls.
deletion of Exon 7 of the CD163 gene, encoding SRCR5 had no adverse effects in pigs and these animals showed complete resistance to viral infection by the positive-strand RNA PRRS virus
CD163 is not necessary for infection with African swine fever virus.
CD163 represents an additional candidate gene for resistance against porcine reproductive and respiratory syndrome.
Overexpression of ADAM17 (show ADAM17 Proteins) induced downregulation of CD163 expression and a reduction in reproductive and respiratory syndrome virus infection.
Fusion protein of sialoadhesin (show SIGLEC1 Proteins) and domains 5-9 of CD163 receptors blocked the respiratory syndrome virus infection.
GP4 (show CD36 Proteins) is involved in interaction with cellular receptor CD163.
). These results provided fundamental evidence for CD163 and SN as two functional candidate genes affecting immunity in pigs.
Porcine reproductive and respiratory syndrome virus GP4 (show CD36 Proteins) was found to co-localize with CD163 in the lipid rafts on the plasma membrane.
Our results suggest that the intracellular domain of CD163 may be associated with an important yet-unknown function during porcine reproductive and respiratory syndrome virus replication.
The newly established porcine alveolar macrophage cell lines were demonstrated to express robust levels of CD163 and to be fully permissive for both type 1 and 2 porcine reproductive and respiratory syndrome virus strains.
The protein encoded by this gene is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. It functions as an acute phase-regulated receptor involved in the clearance and endocytosis of hemoglobin/haptoglobin complexes by macrophages, and may thereby protect tissues from free hemoglobin-mediated oxidative damage. This protein may also function as an innate immune sensor for bacteria and inducer of local inflammation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
, CD163 molecule
, scavenger receptor cysteine-rich type 1 protein M130-like
, scavenger receptor cysteine-rich type 1 protein M130
, hemoglobin scavenger receptor
, macrophage-associated antigen