SLC6A17 anticorps (AA 1-694)

N° du produit ABIN7599527

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

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

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

Attributs du produit: Anti-SLC6A17 Antibody. Tested in ELISA, WB applications. This antibody reacts with Human, Mouse, Rat.

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, -

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.

Date de péremption: 12 months

Détails sur SLC6A17

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

Autre désignation: SLC6A17

Sujet:

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.

Gene Full Name: solute carrier family 6 member 17

Poids moléculaire: 81 kDa

ID gène: 388662

UniProt: Q9H1V8