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VHLL Antikörper (N-Term)

VHLL Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2791981
  • Target Alle VHLL Antikörper anzeigen
    VHLL (Von Hippel-Lindau Tumor Suppressor-Like (VHLL))
    Bindungsspezifität
    • 6
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reaktivität
    Human
    Wirt
    • 6
    • 3
    Kaninchen
    Klonalität
    • 7
    • 2
    Polyklonal
    Konjugat
    • 5
    • 2
    • 1
    • 1
    Dieser VHLL Antikörper ist unkonjugiert
    Applikation
    • 6
    • 3
    • 1
    Western Blotting (WB)
    Sequenz
    PWRAGNGVGL EAQAGTQEAG PEEYCQEELG AEEEMAARAA WPVLRSVNSR
    Homologie
    Human: 100%
    Produktmerkmale
    This is a rabbit polyclonal antibody against VHLL. It was validated on Western Blot.
    Aufreinigung
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the N-terminal region of Human VHLL
    Top Product
    Discover our top product VHLL Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeat freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    VHLL (Von Hippel-Lindau Tumor Suppressor-Like (VHLL))
    Andere Bezeichnung
    VHLL (VHLL Produkte)
    Synonyme
    VHLP antikoerper, VLP antikoerper, VHL like antikoerper, VHLL antikoerper
    Hintergrund
    Von Hippel-Lindau (VHL) tumor suppressor protein is a component of an E3 ubiquitin ligase complex that 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. This gene may contribute to the regulation of oxygen homeostasis and neovascularization during placenta development. This gene is intronless, and can also be interpreted as a retrotransposed pseudogene of the VHL locus located on chromosome 3. However, the protein is represented in this RefSeq due to evidence in PMID:14757845 that strongly suggests it is translated. The same publication also indicates that this protein binds HIF alpha but fails to recruit the E3 ubiquitin ligase complex, and it therefore functions as a dominant-negative VHL protein and a protector of HIF alpha.
    Alias Symbols: VHLP, VLP
    Protein Interaction Partner: RBPMS, DAZAP2, HIF1A,
    Protein Size: 139
    Molekulargewicht
    15 kDa
    Gen-ID
    391104
    NCBI Accession
    NM_001004319, NP_001004319
    UniProt
    Q6RSH7
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