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ADAM8 encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Additionally we are shipping ADAM8 Antibodies (68) and ADAM8 Kits (15) and many more products for this protein.
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Human ADAM8 Protein expressed in HEK-293 Cells - ABIN2180563
Yoshiyama, Higuchi, Kataoka, Matsuura, Yamamoto: CD156 (human ADAM8): expression, primary amino acid sequence, and gene location. in Genomics 1997
Show all 2 references for ABIN2180563
The important role of ADAM8 in the progression of hepatocellular carcinoma induced by diethylnitrosamine in mice
ADAM8 mediates an enhanced invasiveness of neutrophils into injured muscle fibers by the removal of their adhesiveness to blood vessels after infiltration into interstitial tissues.
ADAM8 has anti-inflammatory activities during allergic airway inflammation in mice
overexpression of PrP(C (show PRNP Proteins)) led to up-regulation of ADAM8, suggesting that PrP(C (show PRNP Proteins)) may regulate its own alpha-cleavage through modulating ADAM8 activity.
ADAM-8 appears to favour allergen-induced acute airway inflammation by promoting dendritic cell recruitment and CCL11 and CCL22 (show CCL22 Proteins) production.
ADAM8 knockout mice did not display a bone phenotype in vivo but they did not increase RANKL (show TNFSF11 Proteins) production, OCL (show OCLN Proteins) formation, or calvarial fibrosis in response to tumor necrosis factor alpha (TNF-alpha (show TNF Proteins)) in vivo.
ADAM8 is involved in T cell maturation in the medulla but has a relatively minor impact on T cell development.
The results of this study indicated an essential role for ADAM8 in modulating TNF-alpha (show TNF Proteins) signaling in CNS diseases
The study finds an increase in retinal re-vascularization but fewer neovascular tufts in the oxygen-induced retinopathy model and increased growth of heterotopically injected tumor cells in Adam8-/- mice compared with wild-type controls.
ADAM8 plays a proinflammatory role in airway inflammation.
ADAM8 causes temozolomide resistance in glioblastoma cells by enhancing pAkt/PI3K, pERK1/2, and cleavage of CD44 and HGF R/c-met
ADAM8 promotes GC cell proliferation and invasion, and its expression is positively correlated with poor survival, indicating that it might be a promising target in GC therapy
ADAM8 expression is associated with increased migration and invasiveness of pancreatic ductal adenocarcinoma cells.
ADAM8 and endostatin (show COL18A1 Proteins) play a role in osteosarcoma progression.
Data indicate that fibronectin (show FN1 Proteins) fragments (FN-fs) are present in adult ntervertebral disc (IVD (show IVD Proteins)) from adult subjects, and ADAM-8, known to cleave FN, is present at the pericellular matrix of disc cells.
Results show that ADAM8 is overexpressed in colorectal cancer and promotes cell growth.
N-glycosylation is essential for processing, localization, stability, and activity of ADAM8.
ADAM8 expression is increased in both severe asthma and COPD (show ARCN1 Proteins) and associated with sputum total cell count and neutrophils. ADAM8 may facilitate neutrophil migration to the airways in severe asthma and COPD (show ARCN1 Proteins).
ADAM8 is abundantly expressed in breast tumors and derived metastases compared to normal tissue.
High ADAM8 expression is associated with pancreatic adenocarcinoma.
This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene may be involved in cell adhesion during neurodegeneration, and it is thought to be a target for allergic respiratory diseases, including asthma. Alternative splicing results in multiple transcript variants.
a disintegrin and metalloproteinase domain 8
, ADAM 8
, a disintegrin and metalloprotease domain (ADAM) 8
, a disintegrin and metalloprotease domain 8
, cell surface antigen MS2
, disintegrin and metalloproteinase domain-containing protein 8
, macrophage cysteine-rich glycoprotein
, human leukocyte differentiation antigen
, a disintegrin and metallopeptidase domain 8