DMPK polyclonal antibody

Catalog # PAB24919

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Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of Jurkat cell lysate with DMPK polyclonal antibody (Cat # PAB24919).

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against synthetic peptide of DMPK.

    Immunogen

    A synthetic peptide corresponding to DMPK.

    Host

    Rabbit

    Theoretical MW (kDa)

    70

    Reactivity

    Human

    Specificity

    DMPK polyclonal antibody detects endogenous levels of DMPK protein.

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    1 mg/mL

    Recommend Usage

    Western Blot (1:500-1:1000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.2 (0.05% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage 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 (Cell lysate)

    Western blot analysis of Jurkat cell lysate with DMPK polyclonal antibody (Cat # PAB24919).
  • Gene Info — DMPK

    Entrez GeneID

    1760

    Gene Name

    DMPK

    Gene Alias

    DM, DM1, DM1PK, DMK, MDPK, MT-PK

    Gene Description

    dystrophia myotonica-protein kinase

    Omim ID

    160900 605377

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a serine-threonine kinase that is closely related to other kinases that interact with members of the Rho family of small GTPases. Substrates for this enzyme include myogenin, the beta-subunit of the L-type calcium channels, and phospholemman. The 3' untranslated region of this gene contains 5-37 copies of a CTG trinucleotide repeat. Expansion of this unstable motif to 50-5,000 copies causes myotonic dystrophy type I, which increases in severity with increasing repeat element copy number. Repeat expansion is associated with condensation of local chromatin structure that disrupts the expression of genes in this region. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq

    Other Designations

    DM protein kinase|dystrophia myotonica 1|myotonic dystrophy associated protein kinase|myotonic dystrophy protein kinase|myotonin protein kinase A|thymopoietin homolog

  • Interactome
  • 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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