SLC6A17 anticorps (AA 1-694) (HRP)

N° du produit ABIN8040526

Cet anticorps anti-SLC6A17 Polyclonal Lapin conjugué à HRP (ABIN8040526) détecte spécifiquement SLC6A17 dans WB, ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour SLC6A17 anticorps (AA 1-694) (HRP) (ABIN8040526)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC6A17 est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-SLC6A17 anticorps (HRP)

Épitope: AA 1-694

Fonction: Anti-SLC6A17 Antibody HRP Conjugated

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

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, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. 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

ID gène: 388662

UniProt: Q9H1V8