ECM1 Antilichaam

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.

1893

Q16610

Human

A synthetic peptide corresponding to a sequence within amino acids 150-250 of human ECM1 (NP_001189787.1) .

Unconjugated

Primary Antibodies

Immunology

Affinity purification

MCF7

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 61kDa

IgG

WB: 1:500 - 1:2000

ECM1

A-375

HepG2

Extracellular matrix protein 1

Homo sapiens

URBWD, extracellular matrix protein 1, secretory component p85, testicular tissue protein Li 61

WB

Liquid