SLC6A17 antibody (AA 1-694) (Biotin)

Catalog No. ABIN8040520

The Biotin-conjugated Rabbit Polyclonal anti-SLC6A17 antibody (ABIN8040520) specifically detects SLC6A17 in WB, ELISA and IHC. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for SLC6A17 antibody (AA 1-694) (Biotin) (ABIN8040520)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC6A17 antibody is conjugated to Biotin

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

Product Details anti-SLC6A17 Antibody (Biotin)

Binding Specificity: AA 1-694

Purpose: Anti-SLC6A17 Antibody Biotin Conjugated

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

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: 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

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. 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

Gene ID: 388662

UniProt: Q9H1V8