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SLC29A3 antibody

SLC29A3 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6566901
  • Target See all SLC29A3 Antibodies
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Reactivity
    • 20
    • 6
    • 5
    • 3
    • 3
    Human
    Host
    • 21
    Rabbit
    Clonality
    • 21
    Polyclonal
    Conjugate
    • 9
    • 3
    • 3
    • 2
    • 2
    • 2
    This SLC29A3 antibody is un-conjugated
    Application
    • 20
    • 16
    • 15
    • 4
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human SLC29A3
    Isotype
    IgG
    Top Product
    Discover our top product SLC29A3 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Alternative Name
    SLC29A3 (SLC29A3 Products)
    Synonyms
    ENT3 antibody, HCLAP antibody, HJCD antibody, PHID antibody, Ent3 antibody, 4933435C21Rik antibody, AW987637 antibody, solute carrier family 29 member 3 antibody, solute carrier family 29 (nucleoside transporters), member 3 antibody, SLC29A3 antibody, Slc29a3 antibody
    Background

    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.

    Molecular Weight

    Observed_MW: 50kDa

    Calculated_MW: 35kDa/51kDa

    Gene ID
    55315
    UniProt
    Q9BZD2
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