Myosin 9 anticorps (N-Term)

N° du produit ABIN7464342

Cet anticorps Souris Monoclonal détecte spécifiquement Myosin 9 dans WB, IF, IHC (p), ICC et FACS. Il présente une réactivité envers Humain.

Aperçu rapide pour Myosin 9 anticorps (N-Term) (ABIN7464342)

Antigène: Myosin 9 (MYH9)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Myosin 9 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Flow Cytometry (FACS)

Classe de qualité: KO Validated

Clone: GT218

Détail du produit anti-Myosin 9 anticorps

Épitope: N-Term

Réactivité croisée: Humain, Souris

Purification: Affinity purified by Protein A.

Immunogène: Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.

Isotype: IgG2b

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: A431

Validation: KO/KD

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS pH 7, 20 % Glycerol, No Preservative

Agent conservateur: Without preservative

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur Myosin 9

Antigène: Myosin 9 (MYH9)

Autre désignation: myosin heavy chain 9

Sujet: Myosin heavy chain 9 , BDPLT6 , DFNA17 , EPSTS , FTNS , MATINS , MHA , NMHC-II-A , NMMHC-IIA , NMMHCA,This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq]

Poids moléculaire: 227 kDa

ID gène: 4627

UniProt: P35579

Pathways: Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex