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TTPA antibody (AA 13-278)

TTPA Reactivity: Human, Mouse, Rat WB, ELISA, FACS Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7599931
  • Target See all TTPA Antibodies
    TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
    Binding Specificity
    • 7
    • 2
    • 1
    • 1
    AA 13-278
    Reactivity
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 11
    • 1
    Rabbit
    Clonality
    • 11
    • 1
    Polyclonal
    Conjugate
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    This TTPA antibody is un-conjugated
    Application
    • 11
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Flow Cytometry (FACS)
    Purpose
    Anti-TTPA/TPP1 Antibody Picoband®
    Cross-Reactivity (Details)
    No cross-reactivity with other proteins.
    Characteristics
    Anti-TTPA/TPP1 Antibody Picoband® (ABIN7599931). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
    Purification
    Immunogen affinity purified.
    Immunogen
    E.coli-derived human TTPA/TPP1 recombinant protein (Position: Q13-Q278).
    Isotype
    IgG
    Top Product
    Discover our top product TTPA Primary Antibody
  • Application Notes
    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Arita, M., Sato, Y., Miyata, A., Tanabe, T., Takahashi, E., Kayden, H. J., Arai, H., Inoue, K. Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization. Biochem. J. 306: 437-443, 1995. 2. Cavalier, L., Ouahchi, K., Kayden, H. J., Di Donato, S., Reutenauer, L., Mandel, J.-L., Koenig, M. Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. Am. J. Hum. Genet. 62: 301-310, 1998. 3. Cellini, E., Piacentini, S., Nacmias, B., Forleo, P., Tedde, A., Bagnoli, S., Ciantelli, M., Sorbi, S. A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. Arch. Neurol. 59: 1952-1953, 2002.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Concentration
    500 μg/mL
    Buffer
    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
    Storage
    4 °C,-20 °C
    Storage Comment
    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target
    TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
    Alternative Name
    TTPA (TTPA Products)
    Background

    Synonyms: Interleukin-6, IL-6, Il6, Il-6

    Tissue Specificity: Expressed in activated macrophages (at protein level).

    Background: Alpha-tocopherol transfer protein is a protein that in humans is encoded by the TTPA gene. This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.

    Molecular Weight
    32 kDa, 37 kDa
    Gene ID
    7274
    UniProt
    P49638
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