Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
ECM1 encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. Additionally we are shipping ECM1 Kits (35) and ECM1 Proteins (8) and many more products for this protein.
Showing 10 out of 82 products:
Human Monoclonal ECM1 Primary Antibody for ELISA, EM - ABIN4306907
Tang, Tao, Yun-Liu, Sun, Geng, Jiang: Immunocytochemical localization of secretory component in Paneth cell secretory granules-rat Paneth cells participate in acquired immunity. in Journal of molecular histology 2005
Show all 6 references for ABIN4306907
Overexpression of miR (show MLXIP Antibodies)-486-3p inhibited cell growth and metastasis by targeting ECM1.
For 1q21 loci, we confirmed gene ECM1 as the most plausible gene from this region to be involved in pathogenesis of inflammatory bowel disease
In conclusion, the domain-specific anti-ECM1 MAbs produced in this study should provide a useful tool for investigating ECM1's biological functions, and cellular pathways in which it is involved.
Lipoid proteinosis is a rare autosomal recessive disorder caused by mutations in ECM1, encoding extracellular matrix protein 1, a glycoprotein expressed in many organs and which has important protein-protein interactions in tissue homeostasis
MMP-2 (show MMP2 Antibodies) protein and ECM1 gene are useful preoperative markers for defining malignancy in suspicious thyroid nodules
association between beta-catenin (show CTNNB1 Antibodies) and the MUC1 (show MUC1 Antibodies) cytoplasmic tail was increased by ECM1
Lipoidproteinosis results from a large homozygous deletion of ECM1 gene in a Chinese family.
High extracellular matrix protein-1 expression is associated with the growth, metastasis and angiogenesis of laryngeal carcinoma
This large cohort revealed extensive phenotypic variability in individuals with the same mutation in ECM1.
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis caused by mutations in extracellular matrix protein 1 (ECM1) that involves deposition of basement membrane-like material in the skin and other organs.
HA accumulation primes the vasculature for atherosclerosis by crosslinking and reorganizing the extracellular matrix (ECM (show MMRN1 Antibodies)) and by pushing VSMC differentiation towards a less mature phenotype.
Retinoid signaling in the stroma activates expression of Ecm1, which in turn down-regulates Ret (show RET Antibodies) expression in the ureteric bud cleft, where bifurcation normally occurs and normal branching progresses.
This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene.
extracellular matrix protein 1
, secretory component p85