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Phospholamban Antikörper (pSer16) (PE)

Der Kaninchen Polyklonal Anti-Phospholamban-Antikörper wurde für FACS validiert. Er ist geeignet, Phospholamban in Proben von Human, Ratte und Maus zu detektieren.
Produktnummer ABIN2178506

Kurzübersicht für Phospholamban Antikörper (pSer16) (PE) (ABIN2178506)

Target

Alle Phospholamban (PLN) Antikörper anzeigen
Phospholamban (PLN)

Reaktivität

  • 86
  • 23
  • 21
  • 3
  • 2
  • 2
  • 2
Human, Ratte, Maus

Wirt

  • 87
  • 3
  • 1
Kaninchen

Klonalität

  • 86
  • 5
Polyklonal

Konjugat

  • 45
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser Phospholamban Antikörper ist konjugiert mit PE

Applikation

  • 37
  • 36
  • 26
  • 26
  • 22
  • 11
  • 9
  • 9
  • 9
  • 9
  • 7
  • 6
  • 1
  • 1
Flow Cytometry (FACS)
  • Bindungsspezifität

    • 25
    • 17
    • 12
    • 9
    • 8
    • 8
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer16

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic phosphopeptide derived from human Cardiac phospholamban around the phosphorylation site of Ser16

    Isotyp

    IgG
  • Applikationshinweise

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    Kommentare

    Exitation/Emission: 480,565nm/578nm

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 100 μg/mL BSA, 50 % glycerol and 0.09 % 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

    -20 °C

    Informationen zur Lagerung

    Store at 4 °C for 12 months.
  • Target

    Phospholamban (PLN)

    Andere Bezeichnung

    Plb

    Hintergrund

    Defects in PLN are the cause of cardiomyopathy dilated type 1P (CMD1P) . Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.Defects in PLN are the cause of cardiomyopathy familial hypertrophic type 18 (CMH18) . CMH18 is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
    Synonyms: Phospholamban phospho S16, p-Phospholamban phospho S16, p-PLBS16, Cardiac phospholamban, CMD1P, PLB, PLN, PPLA_HUMAN.

    Gen-ID

    5350

    Pathways

    Negative Regulation of Transporter Activity
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