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PYGM Antikörper (C-Term)

Dieses Anti-PYGM-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von PYGM in WB und IHC (p). Geeignet für Human.
Produktnummer ABIN5531905

Kurzübersicht für PYGM Antikörper (C-Term) (ABIN5531905)

Target

Alle PYGM Antikörper anzeigen
PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Reaktivität

  • 31
  • 23
  • 22
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 48
  • 8
Kaninchen

Klonalität

  • 48
  • 8
Polyklonal

Konjugat

  • 26
  • 7
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser PYGM Antikörper ist unkonjugiert

Applikation

  • 47
  • 21
  • 14
  • 13
  • 13
  • 8
  • 8
  • 7
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Bindungsspezifität

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

    Aufreinigung

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

    Immunogen

    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.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    For WB starting dilution is: 1:1000

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    2 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

    Andere Bezeichnung

    PYGM

    Hintergrund

    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.

    Molekulargewicht

    97 kDa

    Gen-ID

    5837

    UniProt

    P11217

    Pathways

    Cellular Glucan Metabolic Process
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