• Phare
  • Validé par KD/KO

Anticorps Recombinant de lapin anti-ECM1

ECM1 Recombinant Antibody for WB, FC (Intra), ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

WB, FC (Intra), ELISA

Conjugaison

Non conjugué

CloneNo.

230321F12

N° de cat : 83067-6-RR

Synonymes

230321F12, extracellular matrix protein 1, Secretory component p85



Applications testées

Résultats positifs en WBcellules A375, cellules A431, cellules L02
Résultats positifs en FC (Intra)cellules A375,

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
Flow Cytometry (FC) (INTRA)FC (INTRA) : 0.25 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

83067-6-RR cible ECM1 dans les applications de WB, FC (Intra), ELISA et montre une réactivité avec des échantillons Humain

Réactivité Humain
Hôte / Isotype Lapin / IgG
Clonalité Recombinant
Type Anticorps
Immunogène ECM1 Protéine recombinante Eg0533
Nom complet extracellular matrix protein 1
Masse moléculaire calculée 540 aa, 61 kDa
Poids moléculaire observé60-80 kDa
Numéro d’acquisition GenBankBC023505
Symbole du gène ECM1
Identification du gène (NCBI) 1893
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS with 0.02% sodium azide and 50% glycerol
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

ECM1 (extracellular matrix protein 1), also known as URBWD. It is located in secreted, extracellular space, and extracellular matrix, which is mainly expressed in esophagus and gall bladder. The 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. The calculated molecular weight of ECM1 is 60 kDa, and this antibody can recognize the 63 kDa isoform of target, moreover, this protein may have glycosylation modification.

Protocole

Product Specific Protocols
WB protocol for ECM1 antibody 83067-6-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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