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Myosin 9 anticorps (C-Term)

Cet anticorps anti-Myosin 9 est un anticorps Lapin Polyclonal détectant Myosin 9 dans WB. Adapté pour Humain et Souris.
N° du produit ABIN1536807

Aperçu rapide pour Myosin 9 anticorps (C-Term) (ABIN1536807)

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
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB38850
  • Épitope

    • 7
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1840-1867, C-Term

    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 1840-1867 amino acids from the C-terminal region of human MYH9.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:2000. WB: 1:2000

    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

    Stockage commentaire

    MYH9 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -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

    ID gène

    4627

    NCBI Accession

    NP_002464

    UniProt

    P35579

    Pathways

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