TNNI3 polyclonal antibody

Catalog # PAB19126

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Size:100 uL
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of BGC-823 whole cell lystae with TNNI3 polyclonal antibody (Cat # PAB19126) at 1:500 dilution.

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against full length recombinant TNNI3.

    Immunogen

    Recombinant protein corresponding to full length human TNNI3.

    Host

    Rabbit

    Reactivity

    Human

    Specificity

    It can expression in BGC823 whole cell lysate.

    Form

    Liquid

    Recommend Usage

    Western blot (1:500)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In serum

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Cell lysate)

    Western blot analysis of BGC-823 whole cell lystae with TNNI3 polyclonal antibody (Cat # PAB19126) at 1:500 dilution.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — TNNI3

    Entrez GeneID

    7137

    Protein Accession#

    P19429

    Gene Name

    TNNI3

    Gene Alias

    CMD2A, CMH7, MGC116817, RCM1, TNNC1, cTnI

    Gene Description

    troponin I type 3 (cardiac)

    Omim ID

    115210 191044

    Gene Ontology

    Hyperlink

    Gene Summary

    Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). [provided by RefSeq

    Other Designations

    familial hypertrophic cardiomyopathy 7|troponin I, cardiac

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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