6xHis was fused on the N-terminus of the linear polyubiquitin chain binding domain of NEMO encompassing amino acids 183-339. This fusion protein can be used for in vitro pulldown assays and for enrichment of cellular proteins conjugated with linear polyubiquitin chains in whole cell or tissue lysates. 6xHis-NEMO (UBAN) can be precipitated using Nickel resin. After washing, 6xHis-NEMO (UBAN) and its bound proteins can be eluted by a buffer containing 200 mM imidazole.
Additional Information
Product Name: 6xHis-NEMO (UBAN) |
Also Known As: IKBKG; IP; IP1; IP2; FIP3; IPD2; NEMO; FIP-3; Fip3p; AMCBX1; ZC2HC9; IKK-gamma |
Catalog No.: I1521 |
Size: 500 µg |
Molecular Weight: 18.4 kDa |
Species: Human |
Source: Bacterial recombinant |
Stock: 20 mM Tris, 150 mM NaCl, 2 mM βME, 10% Glycerol |
Concentration: See tube label |
Quality Assurance: ~95% by SDS-PAGE, see datasheet for gel image |
Storage: Store at -80°C; avoid multiple freeze-thaw cycles |
PDF Data Sheet: PDF Datasheet, MSDS |
NCBI RefSeq: NM_001099857 |
Image(s): (Click image to enlarge) |
 |
Coomassie-stained SDS-PAGELane 1: Molecular weight markersLane 2: 5 µg purified 6xHis-NEMO (UBAN) |
Shipping Method: Dry ice shipping |
References: 1. van Wijk SJ, et al. (2013) Nat Protoc. 8(7):1449-582. van Wijk SJ, et al. (2012) Mol Cell. 14;47(5):797-809 |
Details
6xHis was fused on the N-terminus of the linear polyubiquitin chain binding domain of NEMO encompassing amino acids 183-339. This fusion protein can be used for in vitro pulldown assays and for enrichment of cellular proteins conjugated with linear polyubiquitin chains in whole cell or tissue lysates. 6xHis-NEMO (UBAN) can be precipitated using Nickel resin. After washing, 6xHis-NEMO (UBAN) and its bound proteins can be eluted by a buffer containing 200 mM imidazole.Images:(Click image to enlarge)
 |
Coomassie-stained SDS-PAGELane 1: Molecular weight markersLane 2: 5 µg purified 6xHis-NEMO (UBAN) |
Note:1. NEMO(183-339) may also bind long polyubiquitin chains linked via lysine 63. 2. Dissolve 10 mM glutathione in a neutral buffer could drop pH to 3-4. Use 0.2 M NaOH to ad-just pH back to neutral.