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抗Mouse (Murine) ADAM12 抗体:
抗Human ADAM12 抗体:
抗Rat (Rattus) ADAM12 抗体:
Human Polyclonal ADAM12 Primary Antibody for IHC (p), IHC - ABIN268655
Isozaki, Rabquer, Ruth, Haines, Koch: ADAM-10 is overexpressed in rheumatoid arthritis synovial tissue and mediates angiogenesis. in Arthritis and rheumatism 2013
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Human Monoclonal ADAM12 Primary Antibody for ELISA, WB - ABIN563531
Zhou, Ran, Hu, Pan, Li, Chen, Sun, Peng, Zhao, Yu, Sun, Yang: TM4SF3 promotes esophageal carcinoma metastasis via upregulating ADAM12m expression. in Clinical & experimental metastasis 2008
Human Polyclonal ADAM12 Primary Antibody for ICC, IF - ABIN4278207
Qundos, Hong, Tybring, Divers, Odeberg, Uhlen, Nilsson, Schwenk: Profiling post-centrifugation delay of serum and plasma with antibody bead arrays. in Journal of proteomics 2013
Human Monoclonal ADAM12 Primary Antibody for ELISA, WB - ABIN393268
Wang, Lu, Zhu, Li: ADAM12 is an effective marker in the second trimester of pregnancy for prenatal screening of Down syndrome. in Prenatal diagnosis 2010
Show all 6 Pubmed References
results suggest that adam12 plays a significant role in the regulation of body growth during juvenile stage in zebrafish, although the precise molecular mechanisms await further study.
In conclusion, MiR29a regulates endothelial cell ADAM12 upregulation in ischemia and this is impaired in hyperglycemia.
It was concluded that TNF-alpha (显示 TNF 抗体)-induced changes in extracellular matix components increased expression of ADAM12 among other changes that were temporally related with the onset of myocyte function.
ADAM12 and ADAM17 (显示 ADAM17 抗体) are essential molecules for the impairment of barrier function of retinal vasculature under hypoxia.
Augmentation of ADAM12 expression in vivo improved outcomes in Balb/c mice, whereas knockdown of ADAM12 made outcomes worse in C57Bl/6 mice. In vitro, ADAM12 expression modulates endothelial cell proliferation, survival, and angiogenesis.
The effect of insulin-like growth factor-I (显示 IGF1 抗体) on ADAM12 expression during the course of myogenesis is reported.
Nitric oxide synthase (显示 NOS 抗体) deficiency has differential effects on ADAM12 expression in growing mouse brain.
Inhibition of Erbb2 (显示 ERBB2 抗体) suppressed the increase in metalloproteinase ADAM12 expression in skin tumors.
TGF-beta (显示 TGFB1 抗体) stimulation of renal cells results in a significant up-regulation of Adams 10, 17, 12, and 19
ADAM12 enhanced ephrin-A1 (显示 EFNA1 抗体) cleavage in response to transforming growth factor-betra1 in primary tumors.
The endogenous SnoN (显示 SKIL 抗体) plays a role in regulating ADAM12 expression in response to TGFbeta1 (显示 TGFB1 抗体).
Tetraspanin-8 (显示 TSPAN8 抗体) has a role in promoting hepatocellular carcinoma metastasis by increasing ADAM12m expression
A novel regulator, myoferlin (显示 MYOF 抗体), of ADAM12 is discovered in HeLa cells and this protein increases ADAM12 expression level, stability, and its enzymatic activity, leading to the reduction of its substrate, E-cadherin (显示 CDH1 抗体), which plays important roles in the regulation of cell adhesion and tumor metastasis.
Our data support a role for ADAM12 in NHL (显示 RTEL1 抗体) cell proliferation, adhesion, and drug resistance, and it may pave the way for a novel therapeutic approach for CAM-DR in NHL (显示 RTEL1 抗体).
The rs3740199 polymorphism in the ADAM12 gene was associated with knee osteoarthritis genetic susceptibility.
These results indicate that ADAM12 actively supports the CSC phenotype in claudin-low breast cancer cells via modulation of the EGFR (显示 EGFR 抗体) pathway.
We conclude that ADAM12 and MMP-14 (显示 MMP14 抗体) are associated with cavernous sinus invasion in pituitary adenomas, which qualifies these proteins in diagnosis and therapy.
ADAM12 expression is significantly upregulated in human masticatory mucosa during wound healing
Stromal expression patterns for both ADAM12 and CDCP1 (显示 CDCP1 抗体).
The first trimester maternal ADAM12-s levels were statistically significantly higher in the entire ART group, IVF (显示 SCN5A 抗体) and ICSI groups, and normal cycle-frozen embryo transfer group when compared with those in the controls.
The level of ADAM12 was upregulated in tumor tissues of breast cancer compared to that of adjacent normal tissues. patients with higher level of ADAM12 exhibited shorter survival time compared to that of low level of ADAM12
These findings suggest ADAM12 is upregulated in muscles with more slow-oxidative myofibres, such as the LM, and is linked to type I myofibers in cattle.
The 5'- and 3'-regions of bovive ADAM12 have been analysed and compared to the human gene, and the promoter region has been cloned and sequenced.
This gene encodes a member of the ADAM (a disintegrin and metalloprotease) protein 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. This gene has two alternatively spliced transcripts: a shorter secreted form and a longer membrane-bound form. The shorter form is found to stimulate myogenesis.
ADAM metallopeptidase domain 12
, ADAM metallopeptidase domain 12 (meltrin alpha)
, a disintegrin and metalloproteinase domain 12 (meltrin alpha)
, ADAM 12
, a disintegrin and metalloprotease domain 12
, disintegrin and metalloproteinase domain-containing protein 12
, meltrin alpha
, ADAM12 short isoform
, disintegrin and metalloprotease 12
, a disintegrin and metallopeptidase domain 12 (meltrin alpha)