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MYBPC3 anticorps (AA 1070-1123)

L’anticorps Lapin Polyclonal anti-MYBPC3 a été validé pour ELISA, WB et IHC. Il convient pour détecter MYBPC3 dans des échantillons de Humain, Rat et Souris. Il y a 1 publication disponible.
N° du produit ABIN5693035

Aperçu rapide pour MYBPC3 anticorps (AA 1070-1123) (ABIN5693035)

Antigène

Voir toutes MYBPC3 Anticorps
MYBPC3 (Myosin Binding Protein C, Cardiac (MYBPC3))

Reactivité

  • 37
  • 33
  • 25
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 48
  • 2
  • 2
Lapin

Clonalité

  • 50
  • 2
Polyclonal

Conjugué

  • 24
  • 6
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MYBPC3 est non-conjugé

Application

  • 42
  • 21
  • 20
  • 13
  • 6
  • 4
  • 4
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 9
    • 7
    • 5
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1070-1123

    Fonction

    Anti-MYBPC3 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-MYBPC3 Antibody Picoband® (ABIN5693035). Tested in ELISA, IHC, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Immunogène

    E. coli-derived human MYBPC3 recombinant protein (Position: Q1070-H1123).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL
    Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL
    ELISA, 0.1-0.5 μg/mL
    1. Calore, C., De Bortoli, M., Romualdi, C., Lorenzon, A., Angelini, A., Basso, C., Thiene, G., Iliceto, S., Rampazzo, A., Melacini, P. A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life. J. Med. Genet. 52: 338-347, 2015. 2. Ehlermann, P., Weichenhan, D., Zehelein, J., Steen, H., Pribe, R., Zeller, R., Lehrke, S., Zugck, C., Ivandic, B. T., Katus, H. A. Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene. BMC Med. Genet. 9: 95, 2008.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Qian, Gong, Yang, Chen, Chen, Xu, Wu, Tang, Gao, Zeng: "Diastolic dysfunction in spontaneous type 2 diabetes rhesus monkeys: a study using echocardiography and magnetic resonance imaging." dans: BMC cardiovascular disorders, Vol. 15, pp. 59, (2015) (PubMed).

  • Antigène

    MYBPC3 (Myosin Binding Protein C, Cardiac (MYBPC3))

    Autre désignation

    MYBPC3

    Sujet

    Synonyms: Myosin-binding protein C, cardiac-type, Cardiac MyBP-C, C-protein, cardiac muscle isoform, MYBPC3

    Tissue Specificity: Red blood cells.

    Background: The myosin-binding protein C, cardiac-type is a protein that in humans is encode by the MYBPC3 gene. MYBPC3 encodes the cardiac isoform of myosin-binding protein C. Myosin-binding protein C is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. MYBPC3, the cardiac isoform, is expressed exclussively in heart muscle. Regulatory phosphorylation of the cardiac isoform in vivo by cAMP-dependent protein kinase (PKA) upon adrenergic stimulation may be linked to modulation of cardiac contraction. Mutations in MYBPC3 are one cause of familial hypertrophic cardiomyopathy.

    Poids moléculaire

    160 kDa

    ID gène

    4607

    UniProt

    Q14896
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