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SLC16A2/MCT8 antibody

SLC16A2 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6569545
  • Target See all SLC16A2/MCT8 (SLC16A2) Antibodies
    SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
    Reactivity
    • 32
    • 28
    • 26
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 32
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 13
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SLC16A2/MCT8 antibody is un-conjugated
    Application
    • 32
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SLC16A2 (NP_006508.2).
    Isotype
    IgG
    Top Product
    Discover our top product SLC16A2 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    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
    SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
    Alternative Name
    SLC16A2 (SLC16A2 Products)
    Synonyms
    MCT8 antibody, AW105741 antibody, Mct8 antibody, Xpct antibody, AHDS antibody, DXS128 antibody, DXS128E antibody, MCT 7 antibody, MCT 8 antibody, MCT7 antibody, MRX22 antibody, XPCT antibody, solute carrier family 16 member 2 antibody, solute carrier family 16 (monocarboxylic acid transporters), member 2 antibody, SLC16A2 antibody, Slc16a2 antibody
    Background
    SLC16A2,AHDS,DXS128,DXS128E,MCT 7,MCT 8,MCT7,MCT8,MRX22,XPCT,This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome.
    Molecular Weight

    Observed_MW: 70kDa

    Calculated_MW: 59kDa

    Gene ID
    6567
    UniProt
    P36021
    Pathways
    Hormone Transport
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