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Myosin 9 anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-Myosin 9 a été validé pour WB et FACS. Il convient pour détecter Myosin 9 dans des échantillons de Humain et Souris.
N° du produit ABIN6243267

Aperçu rapide pour Myosin 9 anticorps (N-Term) (ABIN6243267)

Antigène

Voir toutes Myosin 9 (MYH9) Anticorps
Myosin 9 (MYH9)

Reactivité

  • 64
  • 13
  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 50
  • 12
  • 2
  • 1
  • 1
Lapin

Clonalité

  • 50
  • 16
Polyclonal

Conjugué

  • 40
  • 5
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Myosin 9 est non-conjugé

Application

  • 46
  • 37
  • 17
  • 13
  • 11
  • 9
  • 9
  • 7
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB36361
  • Épitope

    • 8
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 134-165, N-Term

    Homologie

    C, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 134-165 amino acids from the N-terminal region of human MYH9.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. WB: 1:1000. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal 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

    Date de péremption

    6 months
  • Antigène

    Myosin 9 (MYH9)

    Autre désignation

    MYH9

    Sujet

    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.

    Poids moléculaire

    226532

    NCBI Accession

    NP_002464

    UniProt

    P35579

    Pathways

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