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SLC29A3 antibody (N-Term)

SLC29A3 Reactivity: Human WB, IHC (p) Host: Rabbit Polyclonal RB32652 unconjugated
Catalog No. ABIN656792
  • Target See all SLC29A3 Antibodies
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Binding Specificity
    • 7
    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 21-50, N-Term
    Reactivity
    • 19
    • 6
    • 5
    • 3
    • 3
    Human
    Host
    • 20
    Rabbit
    Clonality
    • 20
    Polyclonal
    Conjugate
    • 8
    • 3
    • 3
    • 2
    • 2
    • 2
    This SLC29A3 antibody is un-conjugated
    Application
    • 19
    • 16
    • 15
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This SLC29A3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human SLC29A3.
    Clone
    RB32652
    Isotype
    Ig Fraction
  • Application Notes
    WB: 1:1000. IHC-P: 1:10~50
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    SLC29A3 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    Expiry Date
    6 months
  • Target
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    Alternative Name
    SLC29A3 (SLC29A3 Products)
    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
    51815
    Gene ID
    55315
    NCBI Accession
    NP_001167569, NP_060814
    UniProt
    Q9BZD2
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