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SLC27A2 Antibody / FATP2

Product Specifications

Specifications

Western Blot: 0.25-0.5 µg/mL, Immunohistochemistry: 2-5 µg/mL, Flow cytometry: 1-3ug/million cells, ELISA: 0.1-0.5 µg/mL

UniProt

O14975

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

E.coli-derived human FATP2/SLC27A2 recombinant protein (Position: F27-D608) was used as the immunogen for the SLC27A2 antibody.

Clonality

Polyclonal

Isotype

IgG

Applications

WB, IHC, FACS, ELISA

Purity

Immunogen affinity purified

Format

Lyophilized

Buffer

Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Limitations

This SLC27A2 antibody is available for research use only.

Storage Conditions

After reconstitution, the SLC27A2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Formulation

Adding 0.2 ml of distilled water will yield a concentration of 500 ug/ml

Applications Notes

Optimal dilution of the SLC27A2 antibody should be determined by the researcher.

Location

Cytoplasm (ER), cell membrane

Image Legend

Western blot analysis of SLC27A2 using anti-SLC27A2 antibody. Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. Lane 1: human HepG2 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse liver tissue lysates Lane 7: mouse kidney tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC27A2 antibody at 0.5 ug/ml overnight at 4oC, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal was developed using an ECL Plus Western Blotting Substrate. SLC27A2 western blot across tissues shows the expected ~70 kDa band and a consistent lower band in mouse and rat kidney, consistent with co-expression of the FATP2a and FATP2b splice isoforms and minor PTM-dependent mobility differences.
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