Myosin 9 anticorps

N° du produit ABIN5701128

Cet anticorps anti-Myosin 9 est un anticorps Lapin Polyclonal détectant Myosin 9 dans WB, ELISA, IHC, IF et IP. Adapté pour Humain, Souris, Rat et Poisson zèbre (Danio rerio).

Aperçu rapide pour Myosin 9 anticorps (ABIN5701128)

Antigène: Myosin 9 (MYH9)

Reactivité: Humain, Souris, Rat, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Myosin 9 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)

Détail du produit anti-Myosin 9 anticorps

Fonction: MYH9 antibody

Immunogène: myosin, heavy chain 9, non-muscle

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab05479(MYH9 antibody) at dilution of 1:1000

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur Myosin 9

Antigène: Myosin 9 (MYH9)

Autre désignation: MYH9

Sujet:

Synonyms: Myosin-9|Cellular myosin heavy chain, type A|Myosin heavy chain 9|Myosin heavy chain, non-muscle IIa|Non-muscle myosin heavy chain A (NMMHC-A)|Non-muscle myosin heavy chain IIa (NMMHC II-a, NMMHC-IIA)|MYH9

Background: This gene encodes a conventional non-muscle myosin, this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

Poids moléculaire: 224 kDa

ID gène: 4627

UniProt: P35579

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