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Phospholamban antibody (pSer16) (PE)

The Rabbit Polyclonal anti-Phospholamban antibody has been validated for FACS. It is suitable to detect Phospholamban in samples from Human, Rat and Mouse.
Catalog No. ABIN2178506

Quick Overview for Phospholamban antibody (pSer16) (PE) (ABIN2178506)

Target

See all Phospholamban (PLN) Antibodies
Phospholamban (PLN)

Reactivity

  • 86
  • 23
  • 21
  • 3
  • 2
  • 2
  • 2
Human, Rat, Mouse

Host

  • 87
  • 3
  • 1
Rabbit

Clonality

  • 86
  • 5
Polyclonal

Conjugate

  • 45
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This Phospholamban antibody is conjugated to PE

Application

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  • 22
  • 11
  • 9
  • 9
  • 9
  • 9
  • 7
  • 6
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

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

    Purification

    Purified by Protein A.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

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

    Comment

    Exitation/Emission: 480,565nm/578nm

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at 4 °C for 12 months.
  • Target

    Phospholamban (PLN)

    Alternative Name

    Plb

    Background

    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.

    Gene ID

    5350

    Pathways

    Negative Regulation of Transporter Activity
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