SETD2 polyclonal antibody

Catalog # PAB23943

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

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

Immunohistochemical staining of human oral mucosa with SETD2 polyclonal antibody (Cat # PAB23943) shows moderate nuclear positivity in squamous epithelial cells.

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against recombinant SETD2.

    Immunogen

    Recombinant protein corresponding to amino acids of human SETD2.

    Sequence

    NLGMTSPLPYDSLGYNAPHHPFAGYPPGYPMQAYVDPSNPNAGKVLLPTPSMDPVCSPAPYDHAQPLVGHSTEPLSAPPPVPVVPHVAAPVEVSSSQYVA

    Host

    Rabbit

    Reactivity

    Human

    Form

    Liquid

    Purification

    Antigen affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunohistochemistry (1:1000-1:2500)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.2 (40% glycerol, 0.02% 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

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

    Immunohistochemical staining of human oral mucosa with SETD2 polyclonal antibody (Cat # PAB23943) shows moderate nuclear positivity in squamous epithelial cells.
  • Gene Info — SETD2

    Entrez GeneID

    29072

    Protein Accession#

    Q9BYW2

    Gene Name

    SETD2

    Gene Alias

    FLJ16420, FLJ22472, FLJ23184, FLJ45883, FLJ46217, HIF-1, HSPC069, HYPB, KIAA1732, KMT3A, SET2, p231HBP

    Gene Description

    SET domain containing 2

    Gene Ontology

    Hyperlink

    Gene Summary

    Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein belonging to a class of huntingtin interacting proteins characterized by WW motifs. This protein is a histone methyltransferase that is specific for lysine-36 of histone H3, and methylation of this residue is associated with active chromatin. This protein also contains a novel transcriptional activation domain and has been found associated with hyperphosphorylated RNA polymerase II. [provided by RefSeq

    Other Designations

    SET domain-containing protein 2|histone-lysine N-methyltransferase SETD2|huntingtin interacting protein 1|huntingtin yeast partner B|huntingtin-interacting protein B|lysine N-methyltransferase 3A

  • 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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