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Phospholamban antibody (pSer16, pThr17)

This anti-Phospholamban antibody is a Rabbit Polyclonal antibody detecting Phospholamban in WB. Suitable for Human.
Catalog No. ABIN7269330

Quick Overview for Phospholamban antibody (pSer16, pThr17) (ABIN7269330)

Target

See all Phospholamban (PLN) Antibodies
Phospholamban (PLN)

Reactivity

  • 86
  • 24
  • 22
  • 3
  • 2
  • 2
  • 2
Human

Host

  • 87
  • 3
  • 1
Rabbit

Clonality

  • 86
  • 5
Polyclonal

Conjugate

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  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This Phospholamban antibody is un-conjugated

Application

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  • 22
  • 11
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  • 9
  • 9
  • 9
  • 7
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  • 1
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Western Blotting (WB)
  • Binding Specificity

    • 25
    • 17
    • 11
    • 9
    • 8
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    • 3
    • 3
    • 2
    • 2
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    • 1
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    • 1
    pSer16, pThr17

    Purpose

    Phospho-PLN-S16/T17 Rabbit pAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Phosphorylated Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic phosphorylated peptide around of human Phospho-PLN-S16/T17.

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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 -20°C. Avoid freeze / thaw cycles.
  • Target

    Phospholamban (PLN)

    Alternative Name

    PLN

    Background

    The protein encoded by this gene is found as a pentamer and is a major substrate for the cAMP-dependent protein kinase in cardiac muscle. The encoded protein is an inhibitor of cardiac muscle sarcoplasmic reticulum Ca(2+)-ATPase in the unphosphorylated state, but inhibition is relieved upon phosphorylation of the protein. The subsequent activation of the Ca(2+) pump leads to enhanced muscle relaxation rates, thereby contributing to the inotropic response elicited in heart by beta-agonists. The encoded protein is a key regulator of cardiac diastolic function. Mutations in this gene are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure, and also familial hypertrophic cardiomyopathy.,CMD1P,CMH18,PLB,PLN,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,Calcium Signaling,Cardiovascular,Heart,Contractility,PLN

    Molecular Weight

    6kDa

    Gene ID

    5350

    UniProt

    P26678

    Pathways

    Negative Regulation of Transporter Activity
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