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SLC6A17 antibody (AA 1-694)

The Rabbit Polyclonal anti-SLC6A17 antibody has been validated for WB and ELISA. It is suitable to detect SLC6A17 in samples from Human, Mouse and Rat.
Catalog No. ABIN7599527

Quick Overview for SLC6A17 antibody (AA 1-694) (ABIN7599527)

Target

See all SLC6A17 Antibodies
SLC6A17 (Solute Carrier Family 6, Member 17 (SLC6A17))

Reactivity

  • 16
  • 4
  • 4
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 14
  • 2
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
This SLC6A17 antibody is un-conjugated

Application

  • 16
  • 11
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

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

    Purpose

    Anti-SLC6A17 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    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.

    Purification

    Immunogen affinity purified.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    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.

    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

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

    Alternative Name

    SLC6A17

    Background

    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.

    Molecular Weight

    81 kDa

    Gene ID

    388662

    UniProt

    Q9H1V8
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