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SLC29A3 antibody (AA 1-110)

This Rabbit Polyclonal antibody specifically detects SLC29A3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6147951

Quick Overview for SLC29A3 antibody (AA 1-110) (ABIN6147951)

Target

See all SLC29A3 Antibodies
SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Reactivity

  • 14
  • 5
  • 5
  • 3
  • 3
Human

Host

  • 15
Rabbit

Clonality

  • 15
Polyclonal

Conjugate

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
This SLC29A3 antibody is un-conjugated

Application

  • 15
  • 10
  • 10
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 1-110

    Sequence

    MAVVSEDDFQ HSSNSTYRTT SSSLRADQEA LLEKLLDRPP PGLQRPEDRF CGTYIIFFSL GIGSLLPWNF FITAKEYWMF KLRNSSSPAT GEDPEGSDIL NYFESYLAVA

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human SLC29A3 (NP_060814.4).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    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.,SLC29A3,ENT3,HCLAP,HJCD,PHID,SLC29A3

    Molecular Weight

    35 kDa/51 kDa

    Gene ID

    55315

    UniProt

    Q9BZD2
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