Overview

  • Product nameAnti-MYBPC1 antibody
    See all MYBPC1 primary antibodies
  • Description
    Rabbit polyclonal to MYBPC1
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Mouse, Rat, Human
  • Immunogen

    Synthetic peptide corresponding to 18 amino acids near the N-terminus of Human MYBPC1 (NP_002456).

  • Positive control
    • Rat skeletal muscle tissue lysate

Properties

Applications

Our Abpromise guarantee covers the use of ab124196 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use a concentration of 1 - 2 µg/ml. Predicted molecular weight: 128 kDa.

Target

  • FunctionThick filament-associated protein located in the crossbridge region of vertebrate striated muscle a bands. In vitro it binds MHC, F-actin and native thin filaments, and modifies the activity of actin-activated myosin ATPase. It may modulate muscle contraction or may play a more structural role.
  • Sequence similaritiesBelongs to the immunoglobulin superfamily. MyBP family.
    Contains 3 fibronectin type-III domains.
    Contains 7 Ig-like C2-type (immunoglobulin-like) domains.
  • Information by UniProt
  • Database links
  • Alternative names
    • C protein, skeletal muscle slow isoform antibody
    • C-protein antibody
    • MYBPC1 antibody
    • MYBPCC antibody
    • MYBPCS antibody
    • Myosin binding protein C, slow type antibody
    • Myosin-binding protein C antibody
    • MYPC1_HUMAN antibody
    • skeletal muscle C protein antibody
    • skeletal muscle slow isoform antibody
    • Slow MyBP C antibody
    • Slow MyBP-C antibody
    • slow-type antibody
    see all

Anti-MYBPC1 antibody images

  • Anti-MYBPC1 antibody (ab124196) at 1 µg/ml + Rat skeletal muscle tissue lysate at 15 µg

    Predicted band size : 128 kDa

References for Anti-MYBPC1 antibody (ab124196)

This product has been referenced in:
  • Emmanuele V  et al. Fhl1 W122S causes loss of protein function and late-onset mild myopathy. Hum Mol Genet N/A:N/A (2014). WB ; Mouse . Read more (PubMed: 25274776) »

See 1 Publication for this product

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"