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CCL22 is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Additionally we are shipping CCL22 Kits (103) and CCL22 Proteins (65) and many more products for this protein.
Showing 10 out of 196 products:
Human Polyclonal CCL22 Primary Antibody for ELISA, WB - ABIN1534673
Mosser, Douar, Sarde, Kioschis, Feil, Moser, Poustka, Mandel, Aubourg: Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. in Nature 1993
Show all 2 references for ABIN1534673
Human Polyclonal CCL22 Primary Antibody for ELISA, WB - ABIN334339
Höftberger, Kunze, Weinhofer, Aboul-Enein, Voigtländer, Oezen, Amann, Bernheimer, Budka, Berger: Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: implications for X-linked adrenoleukodystrophy. in Neurobiology of disease 2007
Our results demonstrate that CCL22 is expressed in human placenta. Decidual expression was only observed in miscarriage conditions and correlates with Treg infiltration.
Distinctive Treg associated CCR4 (show CCR4 Antibodies)-CCL22 expression profile with altered frequency of Th17/Treg cell in the immunopathogenesis of Pemphigus Vulgaris (show DSG3 Antibodies).
type I IFN blocks the regulatory T cell-attracting chemokine (show CCL1 Antibodies) CCL22 and thus helps limit the recruitment of regulatory T cells to tumors
First-episode psychosis patients had higher serum CCL22, which decreased substantially following antipsychotic treatment.
Elevated levels of CCL22 found in the ascites could create a chemokine (show CCL1 Antibodies) gradient aiding in Treg cells migration. Increased Tregs percentage in the local microenvironment of ovarian cancer might be an important mechanism of immunosuppression.
Circulating CCL22 levels are related to both glioma risk and survival duration independent of age, histology, grade and IDH (show IDH1 Antibodies) mutation status. CCL22 should be considered a marker of immune status with potential prognostic value
CCL22 is a novel mediator of lung inflammation following hemorrhage and resuscitation
CCR4 (show CCR4 Antibodies) C1014T and CCL22 C16A genetic variations were neither associated with the risk, nor with the progression of colorectal cancer in Iranian population
The serum CCL22 levels were affected by genetic variations at SNP rs223818. Accordingly, SNP rs223818 may play a role in the susceptibility to breast cancer.
Sesamin suppressed lipopolysaccharide induced CCL22 expression in monocytes through the ER/PPAR (show PPARA Antibodies)-a, the MAPK-p38 (show MAPK1 Antibodies) pathway, the NFkB-p65 (show GORASP1 Antibodies) pathway and the epigenetic regulation by suppressing histone H3 (show HIST3H3 Antibodies)/H4 acetylation in the CCL22 promoter region.
CCL22-specific antibodies reveal that engagement of two distinct binding domains on CCL22 is required for CCR4 (show CCR4 Antibodies)-mediated function.
CCL22 was localised mainly on the cell surface and or in the cytoplasm. Within sections of omental milky spot micrometastases, CCR4 (show CCR4 Antibodies) was recognised on or in gastric cancer cells, constituent cells milky spots, blood cells and blood endothelial cells
results show that the IL-4 (show IL4 Antibodies)/CCL22/CCR4 (show CCR4 Antibodies) axis is involved in the migration of Tregs to osteolytic lesion sites, and attenuates development of lesions by inhibiting inflammatory migration and the production of proinflammatory and osteoclastogenic mediators
CCL22 has a role in Treg skin homing to suppress depigmentation
The immunomodulatory properties of CCL22 could be harnessed for prevention of graft rejection and type 1 diabetes as well as other autoimmune disorders.
Data indicate macrophage-derived chemokine CCL22 as an adjuvant could enhance the immune protective effect of NTHi-P6 protein vaccine to an extent.
islet expression of CCL22 recruits Tregs and attenuates autoimmune destruction of beta cell
Data show that the presence of the Ccr4 (show CCR4 Antibodies) and Ccl22 transcripts were detected in brain slices.
These results suggest that CCL22 functions to regulate development of experimental autoimmune encephalomyelitis through macrophage chemoattraction and effector function.
This gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, dendritic cells, natural killer cells and for chronically activated T lymphocytes. It also displays a mild activity for primary activated T lymphocytes and has no chemoattractant activity for neutrophils, eosinophils and resting T lymphocytes. The product of this gene binds to chemokine receptor CCR4. This chemokine may play a role in the trafficking of activated T lymphocytes to inflammatory sites and other aspects of activated T lymphocyte physiology.
chemokine (C-C motif) ligand 22
, C-C motif chemokine 22
, CC chemokine STCP-1
, macrophage-derived chemokine
, small inducible cytokine A22
, small inducible cytokine subfamily A (Cys-Cys), member 22
, small-inducible cytokine A22
, stimulated T cell chemotactic protein 1
, stimulated T-cell chemotactic protein 1
, small inducible cytokine subfamily A (Cys-Cys) member 22
, CC chemokine ABCD-1
, SMALL INDUCIBLE CYTOKINE A22 PRECURSOR (CC CHEMOKINE ABCD-1) (ACTIVATED B AND DENDRITIC CELL-DERIVED)
, activated B and dendritic cell-derived
, dendritic cell and B cell derived chemokine
, small inducible cytokine subfamily A, member 22
, small inducible cytokine subfamily A22