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SLC29A3 Antikörper

SLC29A3 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5967927
  • Target Alle SLC29A3 Antikörper anzeigen
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Reaktivität
    • 20
    • 6
    • 5
    • 3
    • 3
    Human
    Wirt
    • 21
    Kaninchen
    Klonalität
    • 21
    Polyklonal
    Konjugat
    • 9
    • 3
    • 3
    • 2
    • 2
    • 2
    Dieser SLC29A3 Antikörper ist unkonjugiert
    Applikation
    • 20
    • 16
    • 15
    • 4
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human SLC29A3
    Isotyp
    IgG
    Top Product
    Discover our top product SLC29A3 Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Andere Bezeichnung
    SLC29A3 (SLC29A3 Produkte)
    Synonyme
    ENT3 antikoerper, HCLAP antikoerper, HJCD antikoerper, PHID antikoerper, Ent3 antikoerper, 4933435C21Rik antikoerper, AW987637 antikoerper, solute carrier family 29 member 3 antikoerper, solute carrier family 29 (nucleoside transporters), member 3 antikoerper, SLC29A3 antikoerper, Slc29a3 antikoerper
    Hintergrund

    Synonyms: ENT3,Equilibrative nucleoside transporter 3,HCLAP,hENT3,HJCD,PHID,S29A3,SLC29A3,Solute carrier family 29 (equilibrative nucleoside transporter) member 3,Solute carrier family 29 (nucleoside transporters) member 3,Solute carrier family 29 member 3

    Background: This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.

    Molekulargewicht

    Observed_MW: 50kDa

    Calculated_MW: 35kDa/51kDa

    Gen-ID
    55315
    UniProt
    Q9BZD2
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