SLC27A3 antibody (AA 192-683)

Catalog No. ABIN7600438

The Rabbit Polyclonal anti-SLC27A3 antibody is suitable to detect SLC27A3 in samples from Human and Mouse. It has been validated for WB, ELISA and IHC.

Quick Overview for SLC27A3 antibody (AA 192-683) (ABIN7600438)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC27A3 antibody is un-conjugated

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

Product Details anti-SLC27A3 Antibody

Binding Specificity: AA 192-683

Purpose: Anti-FATP3/SLC27A3 Antibody

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

Characteristics: Anti-FATP3/SLC27A3 Antibody. Tested in ELISA, IHC, WB applications. This antibody reacts with Human, Mouse.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human 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 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

Molecular Weight: 70-79 kDa

Gene ID: 11000

UniProt: Q5K4L6