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SLC6A17 Antikörper (AA 1-694)

Der Kaninchen Polyklonal Anti-SLC6A17-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, SLC6A17 in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN7599527

Kurzübersicht für SLC6A17 Antikörper (AA 1-694) (ABIN7599527)

Target

Alle SLC6A17 Antikörper anzeigen
SLC6A17 (Solute Carrier Family 6, Member 17 (SLC6A17))

Reaktivität

  • 16
  • 4
  • 4
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 14
  • 2
Kaninchen

Klonalität

  • 16
Polyklonal

Konjugat

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SLC6A17 Antikörper ist unkonjugiert

Applikation

  • 16
  • 11
  • 1
Western Blotting (WB), ELISA
  • Bindungsspezifität

    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-694

    Verwendungszweck

    Anti-SLC6A17 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-SLC6A17 Antibody Picoband® (ABIN7599527). Tested in ELISA, 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.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human SLC6A17 recombinant protein (Position: M1-Y694).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Mouse, Rat
    ELISA, 0.1-0.5 μg/mL, -
    1. Hoglund, P. J., Adzic, D., Scicluna, S. J., Lindblom, J., Fredriksson, R. The repertoire of solute carriers of family 6: identification of new human and rodent genes. Biochem. Biophys. Res. Commun. 336: 175-189, 2005. 2. Iqbal, Z., Willemsen, M. H., Papon, M.-A., Musante, L., Benevento, M., Hu, H., Venselaar, H., Wissink-Lindhout, W. M., Vulto-van Silfhout, A. T., Vissers, L. E. L. M., de Brouwer, A. P. M., Marouillat, S., Wienker, T. F., Ropers, H. H., Kahrizi, K., Nadif Kasri, N., Najmabadi, H., Laumonnier, F., Kleefstra, T., van Bokhoven, H. Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. Am. J. Hum. Genet. 96: 386-396, 2015.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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

    SLC6A17 (Solute Carrier Family 6, Member 17 (SLC6A17))

    Andere Bezeichnung

    SLC6A17

    Hintergrund

    Synonyms: Histone H3/a, Histone H3/b, Histone H3/c, Histone H3/d, Histone H3/f, Histone H3/h, Histone H3/I, Histone H3/j, Histone H3/k, Histone H3/l, HIST1H3A, HIST1H3B, HIST1H3C, HIST1H3D, HIST1H3E, HIST1H3F, HIST1H3G, HIST1H3H, HIST1H3I, HIST1H3J, H3FJ

    Tissue Specificity: Expressed in fetal brain, fetal lung, fetal liver, heart, brain, placenta, lung, liver, muscle, kidney and pancreas.

    Background: The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability.

    Molekulargewicht

    81 kDa

    Gen-ID

    388662

    UniProt

    Q9H1V8
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