ECM1 Antikörper (Middle Region)

Produktnummer ABIN2782635

Produktdetails anti-ECM1 Antikörper

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

Bindungsspezifität: Middle Region

Reaktivität: Human, Ratte, Maus, Rind (Kuh), Hund, Meerschweinchen, Pferd, Schwein, Kaninchen

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ECM1 Antikörper ist unkonjugiert

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

Sequenz: 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%

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

Aufreinigung: Affinity Purified

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

Anwendungsinformationen

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeat freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Details zu ECM1

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

Andere Bezeichnung: ECM1 (ECM1 Produkte)

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

Hintergrund: 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

Molekulargewicht: 18 kDa

Gen-ID: 1893

NCBI Accession: NM_022664, NP_073155