EML1 monoclonal antibody (M01A), clone 5G3

Catalog # H00002009-M01A

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Size:200 uL
Price: USD $ 335.00
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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)

EML1 monoclonal antibody (M01A), clone 5G3 Western Blot analysis of EML1 expression in HepG2 ( Cat # L019V1 ).

QC Test

Western Blot detection against Immunogen (36.63 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant EML1.

    Immunogen

    EML1 (NP_001008707, 1 a.a. ~ 99 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    MEDGFSSYSSLYDTSSLLQFCNDDSASAASSMEVTDRIASLEQRVQMQEDDIQLLKSALADVVRRLNITEEQQAVLNRKGPTKARPLMQTLPLRTTVNN

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (98); Rat (96)

    Isotype

    IgM Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.63 KDa) .

    Storage Buffer

    In ascites fluid

    Storage Instruction

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

  • Applications

    Western Blot (Cell lysate)

    EML1 monoclonal antibody (M01A), clone 5G3 Western Blot analysis of EML1 expression in HepG2 ( Cat # L019V1 ).

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — EML1

    Entrez GeneID

    2009

    GeneBank Accession#

    NM_001008707

    Protein Accession#

    NP_001008707

    Gene Name

    EML1

    Gene Alias

    ELP79, EMAP, EMAPL, FLJ45033, HuEMAP

    Gene Description

    echinoderm microtubule associated protein like 1

    Omim ID

    602033

    Gene Ontology

    Hyperlink

    Gene Summary

    Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    echinoderm microtubule-associated protein-like

  • 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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