LAT2 monoclonal antibody, clone NAP-03

Catalog # MAB12943

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Size:50 ug
Price: USD $ 531.00
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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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human tonsil with LAT2 monoclonal antibody, clone NAP-03 (Cat # MAB12943) at 5 ug/mL working concentration.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against synthetic peptide of human LAT2.

    Immunogen

    A synthetic peptide (conjugated with KLH) corresponding to amino acids 196-212 of human LAT2.

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A purification

    Isotype

    IgG2a

    Recommend Usage

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (5 ug/mL)
    Immunoprecipitation (1-2 ug/mL)
    Western Blot (1-2 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4 (0.09% 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

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human tonsil with LAT2 monoclonal antibody, clone NAP-03 (Cat # MAB12943) at 5 ug/mL working concentration.

    Immunoprecipitation

  • Gene Info — LAT2

    Entrez GeneID

    7462

    Protein Accession#

    Q9GZY6

    Gene Name

    LAT2

    Gene Alias

    HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5

    Gene Description

    linker for activation of T cells family, member 2

    Omim ID

    605719

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq

    Other Designations

    OTTHUMP00000160648|OTTHUMP00000179118|OTTHUMP00000179119|Williams-Beuren syndrome chromosome region 15|Williams-Beuren syndrome chromosome region 5|linker for activation of B cells|linker for activation of T cells family member 2|non-T cell activation lin

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