ECM1 polyclonal, anti-human

Background:
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.

Synonyms: URBWD

Cellular Location: Cytoplasm

Immunogen:
A synthetic peptide of human ECM1

Gene Symbol: ECM1

Gene ID: 1893

Swiss prot: Q16610

Calculated MW: 61kDa

Recommended dilution:
WB 1:200-1000, IHC 1:10-50,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.