ECM1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES5039-50, ES5039-100

Citations, Manuals and MSDS Available upon request.

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. [provided by RefSeq, Feb 2011],

Alternate Name: ECM1; Extracellular matrix protein 1; Secretory component p85

Source: Rabbit

Applications: IHC; IF; ELISA

Dilution: Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.

Reactivity: Human; Rat; Mouse;

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

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 1893

Human SWISS Prot NO: Q16610

Subcellular Location: Secreted, extracellular space, extracellular matrix.

Research Use Only