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Chitinase 3-like 3, Recombinant, Mouse (Chitinase-3-like Protein 3, ECF-L, Eosinophil chemotactic cytokine, Secreted protein Ym1, Ym1 )

Cat no: C3980-01A

Chitinase 3-like 3, Recombinant, Mouse (Chitinase-3-like Protein 3, ECF-L, Eosinophil chemotactic cytokine, Secreted protein Ym1, Ym1 )

Mouse Chitinase 3-like 3 (CHI3L3), also known as ECF-L (eosinophil chemotactic factor-lymphocyte) or Ym1, is a secreted ~45kD glycoprotein that is a member of the glycosyl hydrolase family 18 (chitinase-like) protein family (1-4). Mouse CHI3L3 has no ortholog in humans, but shares 80% and 90% aa sequence identity with rat CHI3L3 and mouse CHI3L4 (also known as Ym2), respectively (3). Mouse CHI3L3 and CHI3L4 share partial overlap in cell type and tissue mRNA expression (2, 5). CHI3L3 is primarily secreted by alveolar and peritoneal macrophages during inflammation, for example, due to nematode infection and airway hyper-responsiveness (2-10). It is considered a marker for alternatively activated macrophages, and is also expressed in bone marrow myeloid precursors, activated microglia, bone marrow-derived immature mast cells, connective tissue-type mast cells, macrophages in erythroblastic islands, neutrophil granules in bone marrow, peritoneum and spleen red pulp, and IL-4-stimulated B cells and dendritic cells (DC) (2-13). Statins (cholesterol-lowering drugs) can up-regulate CHI3L3 expression in DC and promote Th2 responses (11). CHI3L3 can form crystals when it is at high concentration in the macrophage cytoplasm (2, 3, 12, 13). Reports differ as to its enzymatic and binding properties, but CHI3L3 binding of chitin, GlcN polymer or heparin/heparan sulfate may be weak, and later studies do not indicate significant CHI3L3 chemotactic or enzymatic activity (3-5, 9, 12, 13). However, it is proposed to up-regulate the adhesion molecules LFA-1 (integrin aLB2) and ICAM-1, thus promoting cell-cell adhesion (14). CHI3L3 has also shown activity as a cofactor with RANKL or vitamin D in stimulating osteoclast differentiation (14, 15).\n\nSource:\nRecombinant corresponding to aa1-398 of mouse Chitinase 3-like 3/ECF-L, fused with 6-His tag at C-terminal, expressed in mouse myeloma cell line, NS0.\n\nMolecular Weight: \n~43kD\n\nEndotoxin Level:\n(same/less than)1EU/1ug (LAL)\n\nBiological activity:\nMeasured by the ability of the immobilized protein to support the adhesion of Fadu human squamous cell carcinoma cells (ATCC:HTB-43). When 5x10e4 cells/well are added to recombinant mouse Chitinase 3-like 3 coated plates, cell adhesion is enhanced in a dose dependent manner after 1 hour incubation at 37 degrees C. The ED50 for this effect is typically 0.3-1.2ug/ml.\n\nStorage and Stability:\nLyophilized powder may be stored at -20 degrees C. Stable for 12 months at -20 degrees C. Reconstitute with PBS. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Reconstituted product is stable for 6 months at -20 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

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SPECIFICATIONS

Catalog Number

C3980-01A

Size

50ug

Form

Supplied as a lyophilized powder in PBS. Reconstitute with PBS to 100ug/ml.BSA free.

Purity

~95% (SDS-PAGE)

References

1. Owhashi, M. et al. (2000) J. Biol. Chem. 275:1279. 2. Nio, J. et al. (2004) Histochem. Cell Biol. 121:473. 3. Tsai, M-L. et al. (2004) J. Struct. Biol. 148:290. 4. Chang, N.A. et al. (2001) J. Biol. Chem. 276:17497. 5. Webb, D.C. et al. (2001) J. Biol. Chem. 276:41969. 6. Hung, S-L. et al. (2002) J. Leucoc. Biol. 72:72. 7. Raes, G. et al. (2002) J. Leucoc. Biol. 71:597. 8. Nair, M.G. et al. (2005) Infect. Immun. 73:385. 9. Iwashita, H. et al. (2006) Am. J. Respir. Cell Mol. Biol. 35:103. 10. Welch, J.S. et al. (2002) J. Biol. Chem. 277:42821. 11. Arora, M. et al. (2006) Proc. Natl. Acad. Sci. USA 103:7777. 12. Harbord, M. et al. (2002) J. Biol. Chem. 277:5468. 13. Guo, L. et al. (2000) J. Biol. Chem. 275:8032. 14. Garcia-Palacios, V. et al. (2007) Bone 40:316. 15. Oba, Y. et al. (2003) J. Bone Miner. Res. 18:1332.

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