Recombinant CHD3 anticorps

N° du produit ABIN7828113

Cet anticorps anti-CHD3 Monoclonal Lapin (Clone A479) (ABIN7828113) détecte spécifiquement CHD3 dans WB, IHC, IF et FACS. L’anticorps est réactif avec des échantillons de Humain et Rat.

Aperçu rapide pour Recombinant CHD3 anticorps (ABIN7828113)

Antigène: CHD3 (Chromodomain Helicase DNA Binding Protein 3 (CHD3))

Type d'anticorp: Recombinant Antibody

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp CHD3 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone: A479

Détail du produit anti-CHD3 anticorps

Fonction: Recombinant CHD3 Monoclonal Antibody

Purification: Protein A purified

Immunogène: Recombinant human CHD3 fragment

Isotype: IgG, kappa

Information d'application

Indications d'application: WB 1:500-1:1000,IHC 1:50-1:100,IF 1:50,FCM 1:50-1:100

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Date de péremption: 12 months

Détails sur CHD3

Antigène: CHD3 (Chromodomain Helicase DNA Binding Protein 3 (CHD3))

Autre désignation: CHD3

Sujet: CHD,CHD3,Mi-2a,Mi2-ALPHA,ZFH,chromodomain helicase DNA binding protein 3,Chromodomain-helicase-DNA-binding protein 3(CHD3) is an enzyme that is encoded by the CHD3 gene in human. This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD3 is one of the components of a histone deacetylase complex referred to as the Mi-2/NuRD complex which participates in the remodeling of chromatin by deacetylating histones. Chromatin remodeling is essential for many processes including transcription. Mutations in CHD3 gene cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

Poids moléculaire:

Calculated MW: 227 kDa

Observed MW: 260 kDa The actual band is not consistent with the expectation.

UniProt: Q12873