SLC6A17 anticorps (AA 1-694)

N° du produit ABIN7599527

L’anticorps Lapin Polyclonal anti-SLC6A17 a été validé pour WB et ELISA. Il convient pour détecter SLC6A17 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour SLC6A17 anticorps (AA 1-694) (ABIN7599527)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC6A17 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-SLC6A17 anticorps

Épitope: AA 1-694

Fonction: Anti-SLC6A17 Antibody Picoband®

Réactivité croisée (Details): No cross-reactivity with other proteins.

Attributs du produit: 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.

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

Isotype: IgG

Information d'application

Indications d'application: 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

Stockage

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.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur SLC6A17

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

Autre désignation: SLC6A17

Sujet:

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.

Poids moléculaire: 81 kDa

ID gène: 388662

UniProt: Q9H1V8