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Key Specifications Table
Species Reactivity | Key Applications | Host | Format | Antibody Type |
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M, R, H | WB, ChIP, EMSA | Rb | Serum | Polyclonal Antibody |
Description | |
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Catalogue Number | ABE1928 |
Description | Anti-MafK/Nfe2u Antibody |
Alternate Names |
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Background Information | Transcription factor MafK (UniProt Q61827; also known as Erythroid transcription factor NF-E2 p18 subunit, Nuclear factor erythroid derived 2 ubiquitous, p18 NF-E2) is encoded by the Mafk (also known as Nfe2u, AW061068) gene (Gene ID 17135) in murine species. MafK, MafG and MafF consistute a family of transcription factors that dimerize with the CNC (cap n collar) family regulatory protein Nrf2 (NF-E2 p45-related factor 2) via their bZip domain. The Nrf2/small Maf heterodimer regulates downstream genes, including those of phase II detoxifying enzymes, by targeting antioxidant responsive element (ARE) and Maf recognition element (MARE). |
Product Information | |
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Format | Serum |
Presentation | Rabbit polyclonal serum with 0.05% sodium azide. |
Quality Level | MQ100 |
Applications | |
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Application | This Anti-MafK/Nfe2u Antibody is validated for use in Western Blotting, Chromatin Immunoprecipitation (ChIP) and Electrophoretic Mobility Shift Assay for the detection of MafK/Nfe2u. |
Key Applications |
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Application Notes | Western Blotting Analysis: A representative lot detected endogenous MafK as well as Zn+2-induced expression of exogenous MafK using nuclear extracts from a mouse erythroleukemia (MEL) cell line transfected with MafK cDNA in a metallothionein IIA gene promoter-driven expression plasmid (Igarashi, K., et al. (1995). Proc Natl Acad Sci U S A. 92(16):7445-7449). Chromatin Immunoprecipitation Analysis: A representative lot detected MafK association with the GST-P enhancer (GPE1) in rat hepatoma cells (H4IIE and dRLh84) and hyperplastic nodules/HN-bearing pre-neoplastic rat hepatocytes, but not in normal rat hepatocytes. While MafK association with the NAD(P)H:quinone oxidoreductase 1 (NQO1) antioxidant responsive element (ARE) was detected in all four sample types (Ikeda, H., et al. (2004). Biochem J. 380(Pt 2):515-521). Electrophoretic Mobility Shift Assay Analysis: A representative lot caused a supershift of MafK-containing complex in EMSA using radiolabeled oligonucleotides containing PBGD gene NF-E2 binding site and nuclear extracts from a mouse erythroleukemia (MEL) cell line induced to overexpress MafK (Igarashi, K., et al. (1995). Proc Natl Acad Sci U S A. 92(16):7445-7449). Electrophoretic Mobility Shift Assay (EMSA): A representative lot caused a supershift of both the constitutive and tBHQ-induced ARE-binding complex (Complex I and II, respectively) in EMSA using a radiolabeled oligonucleotide containing antioxidant responsive element (ARE) NF-E2 binding site and nuclear extracts from untreated and tBHQ-treated K562 cells (Kim, Y.C., et al. (2003). Oncogene. 22(12):1860-1865). |
Biological Information | |
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Immunogen | Maltose binding protein-tagged recombinant protein corresponding to mouse MafK/Nfe2u. |
Concentration | Please refer to lot specific datasheet. |
Host | Rabbit |
Species Reactivity |
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Antibody Type | Polyclonal Antibody |
Entrez Gene Number |
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Gene Symbol |
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Purification Method | Unpurified |
UniProt Number |
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Molecular Weight | ~18 kDa observed. Uncharacterized band(s) may appear in some lysates. |
Product Usage Statements | |
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Quality Assurance | Evaluated by Western Blotting in MEL (mouse erythroleukemia) cell lysate. Western Blotting Analysis: 1:2,000 dilution of this antibody detected MafK/NF-E2 in 20 µg of MEL (mouse erythroleukemia) cell lysate. |
Usage Statement |
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Storage and Shipping Information | |
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Storage Conditions | 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. |
Packaging Information | |
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Material Size | 100 µL |