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PYGM anticorps (C-Term)

Cet anticorps anti-PYGM est un anticorps Lapin Polyclonal détectant PYGM dans WB et IHC (p). Adapté pour Humain.
N° du produit ABIN5531905

Aperçu rapide pour PYGM anticorps (C-Term) (ABIN5531905)

Antigène

Voir toutes PYGM Anticorps
PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Reactivité

  • 32
  • 24
  • 20
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 46
  • 8
Lapin

Clonalité

  • 46
  • 8
Polyclonal

Conjugué

  • 25
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PYGM est non-conjugé

Application

  • 46
  • 20
  • 15
  • 13
  • 13
  • 8
  • 7
  • 6
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 15
    • 7
    • 5
    • 3
    • 2
    • 1
    • 1
    AA 698-727, C-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis

    Immunogène

    This PYGM antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 698-727 amino acids from the C-terminal region of human PYGM.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    For IHC-P starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    2 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

    Autre désignation

    PYGM

    Sujet

    PYGM catalyzes and regulates the breakdown of glycogen to glucose-1-phosphate. Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5), also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.

    Poids moléculaire

    97 kDa

    ID gène

    5837

    UniProt

    P11217

    Pathways

    Cellular Glucan Metabolic Process
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