MBL

CircuLex Mouse FABP4/A-FABP ELISA Kit

Product Code:
 
MBL-CY-8077
Product Group:
 
ELISA Kits
Supplier:
 
MBL
Host Type:
 
Mouse
Regulatory Status:
 
RUO
Application:
 
Enzyme-Linked Immunosorbent Assay (ELISA)
Shipping:
 
4°C
Storage:
 
4°C
1 / 1

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  • Further Information
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Further Information

Alternative Names:
Adipocyte-specific fatty acid?binding protein
Background:
Adipocyte-specific fatty acid?binding protein (AFABP), also designated aP2 and FABP4, belongs to the fatty acid-binding protein super family whose members have relative molecular masses of ~15, 000, and it is exclusively expressed in differentiated adipocytes (1, 2). FABP4 is a predominant cytosolic protein of mature adipocytes, accounting for ~6 % of total cellular proteins. This protein may be an important regulator of systemic insulin sensitivity and lipid and glucose metabolism (1). Mice deficient in aP2/FABP4 are protected from development of hyperinsulinemia, hyperglycemia, and insulin resistance in the context of both dietary and genetic obesity (3, 4). Adipocytes obtained from aP2/FABP4-null mice had markedly reduced efficiency of lipolysis in vivo and in vitro (5, 6) and exhibited a 2- to 3-fold decrease in fatty acid release, suggesting that FABP4 mediates efflux of fatty acids in normal physiology (7). Although the physiological consequences of aP2/FABP4 deficiency have been predominantly linked to changes in adipocytes, it has reported that the presence of aP2/FABP4 in macrophages (2, 8) and have shown that aP2/FABP4 expression can be induced by peroxisome proliferatoractivated receptor gamma (PPAR gamma) agonists (8), by toll-like receptor agonists (9), oxidized LDL (10), and the differentiation of monocytes to macrophages and can be suppressed by treatment with a cholesterol-lowering statin (11). In these cells, aP2/FABP4 modulates inflammatory cytokine production and cholesterol ester accumulation (12). In apolipoprotein E-deficient mice, ablation of the aP2/FABP4 gene conferred remarkable protection against atherosclerosis, which commonly occurs in this mouse strain (13, 14). Taken together, these animal studies demonstrate that aP2/FABP4, by integrating metabolic and inflammatory pathways, provides a key link between various components of metabolic syndrome. Moreover, Masato Furuhashi, M. et al. (2007) reported that an orally active small-molecule inhibitor of aP2/FABP4 is an effective therapeutic agent against severe atherosclerosis and type 2 diabetes in mouse models (15).
Description:
The CircuLex Research Product Mouse FABP4/AFABP ELISA kit is used for the quantitative measurement of mouse FABP4/AFABP in serum, plasma, tissue culture medium and other biological media.
Gene IDs:
Human: 2167 Mouse: 11770
Kit Components:
Microplate, 10X Wash Buffer, Dilution Buffer, Mouse FABP4/A-FABP Standard, HRP conjugated Detection Antibody, Substrate Reagent, Stop Solution
Measurement Range:
Results exceeding FABP4/AFABP level of 1,000 ng/ml should be repeated with diluted samples. Dilution factors need to be taken into consideration in calculating the FABP4/AFABP concentration.
Sensitivity:
better than 34.4 pg/ml of sample.
Target:
FABP4/AFABP

Documents

References

1. Makowski L, Hotamisligil GS. J Nutr (2004) 134: 2464S?8S. 2. Boord JB, Fazio S, Linton MF. Curr Opin Lipidol (2002) 13: 141?7. 3. Uysal KT, Scheja L, Wiesbrock SM, Bonner-Weir S, Hotamisligil GS. Endocrinology (2000) 141: 3388?96. 4. Hotamisligil GS, Johnson RS, Distel RJ, Ellis R, Papaioannou VE, Spiegelman BM. Science (1996) 274: 1377?9. 5. Coe NR, Simpson MA, Bernlohr DA. J Lipid Res (1999) 40: 967?72. 6. Scheja L, Makowski L, Uysal KT et al. Diabetes (1999) 48: 1987?94. 7. Baar RA, Dingfelder CS, Smith LA, Bernlohr DA, Wu C, Lange AJ, et al. Biochem Biophys Res Commun (1999) 261: 456?8. 9. Kazemi MR, McDonald CM, Shigenaga JK, Grunfeld C, Feingold KR. Arterioscler Thromb Vasc Biol (2005) 25: 1220?4. 10. Fu Y, Luo N, Lopes-Virella MF. J Lipid Res. (2000) 41: 2017?23.11. Llaverias G, Noe V, Penuelas S, Vazquez-Carrera M, Sanchez RM, Laguna JC, et al. Biochem Biophys Res Commun (2004) 318: 265?74. 12. Makowski L, Brittingham KC, Reynolds JM, Suttles J, Hotamisligil GS. J Biol Chem (2005) 280: 12888?95. 13. Makowski L, Boord JB, Maeda K, Babaev VR, Uysal KT, Morgan MA, et al. Nat Med (2001) 7: 699?705. 14. Boord JB, Maeda K, Makowski L, Babaev VR, Fazio S, Linton MF, et al. Circulation (2004) 110: 1492?8. 15. M Furuhashi, G Tuncman, CZ Gorgun, L Makowski, G Atsumi, E Vaillancourt, K Kono, VR Babaev, S Fazio, MF Linton, R Sulsky, JA Robl, RA Parker, and GS Hotamisligil. Nature (2007) 447: 959-65.