ECM1 anticorps (Middle Region)

N° du produit ABIN2782635

Détail du produit anti-ECM1 anticorps

Antigène: ECM1 (Extracellular Matrix Protein 1 (ECM1))

Épitope: Middle Region

Reactivité: Humain, Rat, Souris, Boeuf (Vache), Chien, Cobaye, Cheval, Porc, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ECM1 est non-conjugé

Application: Immunohistochemistry (IHC), Western Blotting (WB)

Séquence: QDRSQGGWGH RLDGFPPGRP SPDNLNQICL PNRQHVVYGP WNLPQSSYSH

Homologie: Cow: 93%, Dog: 93%, Guinea Pig: 86%, Horse: 93%, Human: 100%, Mouse: 100%, Pig: 93%, Rabbit: 93%, Rat: 100%

Attributs du produit: This is a rabbit polyclonal antibody against ECM1. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of Human ECM1

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur ECM1

Antigène: ECM1 (Extracellular Matrix Protein 1 (ECM1))

Autre désignation: ECM1 (ECM1 Produits)

Synonymes: anticorps URBWD, anticorps ECM, anticorps EMILIN4, anticorps GPIa*, anticorps MMRN, anticorps AI663821, anticorps p85, anticorps extracellular matrix protein 1, anticorps multimerin 1, anticorps ECM1, anticorps MMRN1, anticorps Ecm1

Sujet: 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.
Alias Symbols: -
Protein Interaction Partner: IL2RB, HECW2, SRPK1, CPTP, IRAK3, BNIP3L, ATN1, RERE, UBC, HSPG2, FBLN1,
Protein Size: 170

Poids moléculaire: 18 kDa

ID gène: 1893

NCBI Accession: NM_022664, NP_073155