TNNI3 monoclonal antibody, clone TPC-110

Catalog # MAB1417

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Size:1 mg
Price: USD $ 638.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Mouse monoclonal antibody raised against native human TNNI3.

    Immunogen

    Native purified human TNNI3.

    Host

    Mouse

    Reactivity

    Human

    Specificity

    Human Troponin I, amino acid sequence N24-40. Not reactive to human skeletal muscle Troponin I, human skeletal Troponin T, human cardiac Troponin T, or human Troponin C.

    Form

    Liquid

    Purification

    DEAE column chromatography

    Activity

    Affinity Constant: 4 x 1010 l/mol.

    Isotype

    IgG1

    Recommend Usage

    For solid phase coating (capture) or enzyme conjugation (detection).
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 15 mM KPO4 buffer, 0.85% NaCl, pH 7.4 (0.09% sodium azide).

    Storage Instruction

    Store at 4°C. Do Not Freeze. Precipitation may occur upon freezing.

    Note

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

  • Applications

    Sandwich ELISA

  • Gene Info — TNNI3

    Entrez GeneID

    7137

    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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