Anti-CGI-58 Antibody

1-acylglycerol-3-phosphate O-acyltransferase ABHD5 (EC:2.3.1.51; UniProt Q9DBL9; also known as Abhydrolase domain-containing protein 5, CGI-58, Comparative gene identification-58, Lipid droplet-binding protein CGI-58) is encoded by the Abhd5 (also known as CDS, IECN5, NCIE2, 1300003D03Rik, 2010002J10Rik) gene in murine species (Gene ID 67469). The comparative gene identification-58 (CGI-58) functions as a cofactor of adipose triglyceride lipase/ATGL-mediated triacylglycerol (TG) hydrolytic activity, which is essential for efficient catabolism of cellular TG stores. Mutations in the genes coding for ATGL or CGI-58 in humans cause neutral lipid storage disease characterized by TG accumulation in multiple tissues. CGI-58 gene mutations provoke severe ichthyosis and hepatosteatosis in humans and mice. Mice lacking CGI-58 exclusively in muscle (CGI-58KOM) show TG accumulation in both skeletal and cardiac muscle tissues and develop severe cardiac steatosis and cardiomyopathy as a result of impaired TG catabolism and mitochondrial fatty acid oxidation. Immunocytochemistry analysis reveals diffuse cytoplasmic staining of CGI-58 in 3T3-L1 preadipocytes, while CGI-58 staining is found exclusively on the surface of lipid droplets in differentiated 3T3-L1 adipocytes. CGI-58 binds to lipid droplets by interacting with perilipin C-terminal sequence, while activation of cellular PKA disperses CGI-58 localization from the lipid droplets to cytosol.

~42 kDa observed. CGI-58 migrates with an apparent molecular size slightly larger than the calculated molecular weight of 39.2 kDa for mouse CGI-58.

His-tagged recombinant protein corresponding to mouse CGI-58.

Detect CGI-58 using this Anti-CGI-58 Antibody validated for use in Western Blotting and Immunocytochemistry.

Immunocytochemistry Analysis: A 1:5,000 dilution from a representative lot detected CGI-58 in 3T3-L1 adipocytes (Data courtesy of Dawn Brasaemle, Rutgers University).
Western Blotting Analysis: A representative lot detected recombinant CGI-58, as well as endogenous CGI-58 in differentiated 3T3-L1 adipocytes, and 3T3-L1 preadipocytes stably expressing ectopic perilipin A or perilipin B (Subramanian, V., et al. (2004). J. Biol. Chem. 279(40):42062-42071).
Immunocytochemistry Analysis: A representative lot detected CGI-58 in 3T3-L1 adipocytes, 3T3-L1 preadipocytes stably expressing perilipin A (Subramanian, V., et al. (2004). J. Biol. Chem. 279:42062-42071).
Western Blotting Analysis: A representative lot detected CGI-58 in mouse cardiac muscle, liver, white and brown adipose tissue (Zierler, K.A., et al. (2013). J. Biol. Chem. 288(14):9892-9904).
Western Blotting Analysis: A representative lot detected CGI-58 in in mouse OP9 adipocytes and brown adipose tissue (Skinner, J.R., et al. (2013). Adipocyte. 2(2):80-86).

Research Category
Signaling

Research Sub Category
Signaling Neuroscience

Rabbit polyclonal serum with 0.05% sodium azide.

Unpurified

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Evaluated by Western Blotting in differentiated 3T3-L1 adipocytes cell lysate.

Western Blotting Analysis: A 1:1,000 of this antibody detected CGI-58 in 10 µg of differentiated 3T3-L1 adipocytes cell lysate.

Concentration: Please refer to lot specific datasheet.

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.