ECM1 Polyclonal Antibody

Background:
extracellular matrix protein 1(ECM1) Homo sapiens 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. [provided by RefSeq, Feb 2011],

Alternative Names:
ECM1, Extracellular matrix protein 1, Secretory component p85

Immunogen: Synthesized peptide derived from the N-terminal region of human ECM1.

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

GeneID: ECM1

Storage: -20°C/1 year

NOTE: For Research Use Only