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ubpbio/6xHis-NEMO (UBAN)/I1521/500 µg
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: Also Known As: Catalog No.: Size: Molecular Weight: Species: Source: Stock: Concentration: Quality Assurance: Storage: PDF Data Sheet: NCBI RefSeq: Image(s): Shipping Method: References:
6xHis-NEMO (UBAN)
IKBKG; IP; IP1; IP2; FIP3; IPD2; NEMO; FIP-3; Fip3p; AMCBX1; ZC2HC9; IKK-gamma
I1521
500 µg
18.4 kDa
Human
Bacterial recombinant
20 mM Tris, 150 mM NaCl, 2 mM βME, 10% Glycerol
See tube label
~95% by SDS-PAGE, see datasheet for gel image
Store at -80°C; avoid multiple freeze-thaw cycles
PDF DatasheetMSDS
NM_001099857
(Click image to enlarge)
Coomassie-stained SDS-PAGELane 1: Molecular weight markersLane 2: 5 µg purified 6xHis-NEMO (UBAN)
Dry ice shipping
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.