NOTCH3 anticorps (C-Term)

N° du produit ABIN1537680

Cet anticorps anti-NOTCH3 Monoclonal Souris (Clone 487CT6-9-2) (ABIN1537680) détecte spécifiquement NOTCH3 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour NOTCH3 anticorps (C-Term) (ABIN1537680)

Antigène: NOTCH3 (Notch 3 (NOTCH3))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp NOTCH3 est non-conjugé

Application: Western Blotting (WB)

Clone: 487CT6-9-2

Détail du produit anti-NOTCH3 anticorps

Épitope: AA 2291-2321, C-Term

Purification: This antibody is purified through a protein G column, followed by dialysis against PBS.

Immunogène: This NOTCH3 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 2291-2321 amino acids from the C-terminal region of human NOTCH3.

Isotype: IgG1

Information d'application

Indications d'application: WB: 1:2000. WB: 1:100~250

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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.

Stock: 4 °C,-20 °C

Stockage commentaire: NOTCH3 Antibody (C-term Q2306) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur NOTCH3

Antigène: NOTCH3 (Notch 3 (NOTCH3))

Autre désignation: NOTCH3

Sujet: This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq].

Poids moléculaire: 243631

ID gène: 4854

NCBI Accession: NP_000426

UniProt: Q9UM47

Pathways: Signalisation Notch