SLC6A17 antibody (AA 1-694)

Catalog No. ABIN8040530

This Rabbit Polyclonal antibody specifically detects SLC6A17 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for SLC6A17 antibody (AA 1-694) (ABIN8040530)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC6A17 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Grade: Carrier-free

Product Details anti-SLC6A17 Antibody

Binding Specificity: AA 1-694

Purpose: Anti-SLC6A17 Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

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

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Mouse, Rat ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

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.

Expiry Date: 12 months

Target Details for SLC6A17

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

Alternative Name: SLC6A17

Background:

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

Molecular Weight: 81 kDa

Gene ID: 388662

UniProt: Q9H1V8