SLC27A3 antibody (AA 192-683) (Cy3)

Catalog No. ABIN7990049

The Cy3-conjugated Rabbit Polyclonal anti-SLC27A3 antibody (ABIN7990049) specifically detects SLC27A3 in FACS. The antibody is reactive with Human and Mouse samples.

Quick Overview for SLC27A3 antibody (AA 192-683) (Cy3) (ABIN7990049)

Target: SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC27A3 antibody is conjugated to Cy3

Application: Flow Cytometry (FACS)

Product Details anti-SLC27A3 Antibody (Cy3)

Binding Specificity: AA 192-683

Purpose: Anti-FATP3/SLC27A3 Antibody Cy3 Conjugated

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human FATP3/SLC27A3 recombinant protein (Position: L192-I683).

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, 1-3 μg/1x10⁶ cells

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. Protect from light.

Expiry Date: 12 months

Target Details for SLC27A3

Target: SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

Alternative Name: SLC27A3

Background:

Background: Long-chain fatty acid transport protein 3 is a protein that in humans is encoded by the SLC27A3 gene. This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants.

Gene Full Name: solute carrier family 27 member 3

Gene ID: 11000

UniProt: Q5K4L6