VHLL purified MaxPab mouse polyclonal antibody (B01P)

Catalog # H00391104-B01P

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Size:50 ug
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 (Transfected lysate)
Application

Western Blot (Transfected lysate)

Western Blot analysis of VHLL expression in transfected 293T cell line (H00391104-T01) by VHLL MaxPab polyclonal antibody.

Lane 1: VHLL transfected lysate(15.3 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a full-length human VHLL protein.MaxPab Polyclonal Antibody,MaxPab Polyclonal Antibodies,MaxPab,DNA Immune,DNA Immunization,Immune Technology

    Immunogen

    VHLL (ADR83480.1, 1 a.a. ~ 139 a.a) full-length human protein.

    Sequence

    MPWRAGNGVGLEAQAGTQEAGPEEYCQEELGAEEEMAARAAWPVLRSVNSRELSRIIICNHSPRIVLPVWLNYYGKLLPYLTLLPGRDFRIHNFRSHPWLFRDARTHDKLLVNQTELFVPSSNVNGQPVFANITLQCIP

    Host

    Mouse

    Reactivity

    Human

    Quality Control Testing

    Antibody reactive against mammalian transfected lysate.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

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

  • Applications

    Western Blot (Transfected lysate)

    Western Blot analysis of VHLL expression in transfected 293T cell line (H00391104-T01) by VHLL MaxPab polyclonal antibody.

    Lane 1: VHLL transfected lysate(15.3 KDa).
    Lane 2: Non-transfected lysate.
  • Gene Info — VHLL

    Entrez GeneID

    391104

    GeneBank Accession#

    HQ258729.1

    Protein Accession#

    ADR83480.1

    Gene Name

    VHLL

    Gene Alias

    VLP

    Gene Description

    von Hippel-Lindau tumor suppressor-like

    Gene Ontology

    Hyperlink

    Gene Summary

    Von Hippel-Lindau (VHL) tumor suppressor protein is a component of an E3 ubiquitin ligase complex that the selectively ubiquitinates the alpha subunit of the hypoxia-inducible factor (HIF) transcription factor for proteasome-mediated degradation. Inactivation of VHL causes VHL disease and sporadic kidney cancer. This gene encodes a VHL homolog that lacks one of two key domains necessary for VHL function. It binds HIF alpha but fails to recruit the E3 ubiquitin ligase complex, and therefore functions as a dominant-negative VHL and a protector of HIF alpha. This gene is intronless and predominantly expressed in the placenta, and may contribute to the regulation of oxygen homeostasis and neovascularization during placenta development. [provided by RefSeq

    Other Designations

    von-Hippel-Lindau-like protein

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