TNNI3 (phospho T142) polyclonal antibody

Catalog # PAB31629

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Size:100 uL
Price: USD $ 346.00
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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

    Rabbit polyclonal antibody raised against synthetic peptide of human TNNI3 (phospho T142).

    Immunogen

    A synthetic peptide corresponding to amino acids 80-160 of human TNNI3 (phospho T142).

    Host

    Rabbit

    Reactivity

    Human, Mouse, Rat

    Specificity

    This antibody detects endogenous levels of TNNI3 protein only when phosphorylated at T142.

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    ELISA (1:20000)
    Western Blot (1:500-2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS (50% glycerol, 0.5% BSA and 0.02% sodium azide).

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

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

  • Applications

    Western Blot

    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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