MYH10 anticorps (AA 1150-1450)

N° du produit ABIN5704598

L’anticorps Lapin Polyclonal anti-MYH10 a été validé pour WB, IP, ELISA et IF. Il convient pour détecter MYH10 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour MYH10 anticorps (AA 1150-1450) (ABIN5704598)

Antigène: MYH10 (Myosin, Heavy Polypeptide 10, Non-Muscle (MYH10))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYH10 est non-conjugé

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

Détail du produit anti-MYH10 anticorps

Épitope: AA 1150-1450

Fonction: MYH10 antibody

Immunogène:

Immunogen sequence: 1150-1450aa

Immunogen: myosin, heavy chain 10, non-muscle

Isotype: IgG

Information d'application

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

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 MYH10

Antigène: MYH10 (Myosin, Heavy Polypeptide 10, Non-Muscle (MYH10))

Autre désignation: MYH10

Sujet:

Synonyms: Myosin-10|Cellular myosin heavy chain, type B|Myosin heavy chain 10|Myosin heavy chain, non-muscle IIb|Non-muscle myosin heavy chain B (NMMHC-B)|Non-muscle myosin heavy chain IIb (NMMHC II-b, NMMHC-IIB)|MYH10

Background: This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin, it should not be confused with the unconventional myosin-10 (MYO10). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene have been associated with May-Hegglin anomaly and developmental defects in brain and heart. Multiple transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 200 kDa

ID gène: 4628

UniProt: P35580