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ApoJ/Clusterin, mouse recombinant protein
TRPM-2, Apolipoprotein J, APO-J, CLI, CLU, SGP-2, AAG4, KUB1, SGP2, SP-40, TRPM2, MGC24903.
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q06890 |
|---|---|
| Concentration | 1 |
| Calculated MW | ~45 kDa (SDS-PAGE). Mouse nuclear Clusterin (aa 22-448) is fused at the C-terminus to a His-tag. |
| Gene ID | 12759 |
|---|---|
| Gene Symbol | CLU |
| Other Names | TRPM-2, Apolipoprotein J, APO-J, CLI, CLU, SGP-2, AAG4, KUB1, SGP2, SP-40, TRPM2, MGC24903. |
| Gene Source | Mouse |
| Source | E. coli |
| Assay&Purity | SDS-PAGE; ≥90% |
| Assay2&Purity2 | N/A; |
| Recombinant | Yes |
| Target/Specificity | ApoJ/Clusterin |
| Format | Liquid |
| Storage | -20°C; 1 mg/ml of 0.2 µm-filtered solution in 55 mM Tris-Cl, pH 8.2, containing 150 mM NaCl. |
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Provided below are standard protocols that you may find useful for product applications.
Background
Native Apolipoprotein J (ApoJ), also named Clusterin, is a heavily glycosylated, 75-80 kDa disulfide-linked heterodimeric protein. Despite being cloned since 1989, no genuine function has been attributed to ApoJ so far. The protein has been reportedly implicated in several diverse physiological processes such as sperm maturation, lipid transportation, complement inhibition, tissue remodeling, membrane recycling, cell-cell and cell-substratum interactions, stabilization of stressed proteins in a folding-competent state and promotion or inhibition of apoptosis. ApoJ gene is differentially regulated by cytokines, growth factors and stress-inducing agents. Clusterin is up- or down regulated on the mRNA or protein level in many pathological and clinically relevant situations including cancer, organ regeneration, infection, Alzheimer disease, retinitis pigmentosa, myocardial infarction, renal tubular damage, autoimmunity and others.
References
Lee K.-H.,et al.Biochem. Biophys. Res. Commun. 194:1175-1180(1993).
French L.E.,et al.J. Cell Biol. 122:1119-1130(1993).
Jordan-Starck T.C.,et al.J. Lipid Res. 35:194-210(1994).
Hodgdon B.A.,et al.Submitted (NOV-1992) to the EMBL/GenBank/DDBJ databases.
McLaughlin L.,et al.J. Clin. Invest. 106:1105-1113(2000).
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