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  • 實驗方法> 蛋白質技術> 蛋白分離純化>Purification of 6xHis epitope tagged proteins by Ni-NTA-Agarose His標簽蛋白純化

    Purification of 6xHis epitope tagged proteins by Ni-NTA-Agarose His標簽蛋白純化

    關鍵詞: 蛋白純化 Ni-NTA-Agarose 6xHis來源: 互聯網

    Low (“Low”)Imidazole Buffer 0.5L

    100mM Imidizole 3.4g

    5% glycerol 25ml 100% glycerol

    50mM Tris-HCl (pH 7.9)50ml 0.5M Tris-HCl (pH 7.9)

    0.1% Tween-20 0.5M 100% Tween-20

    500mM NaCl50ml 5M NaCl

    dH2O Fill to 0.5L (start w/ 350ml)

    High (“High”)Imidazole Buffer 0.5L

    500mM Imidizole 17.0g

    5% glycerol 25ml 100% glycerol

    50mM Tris-HCl (pH 7.9)50ml 0.5M Tris-HCl (pH 7.9)

    0.1% Tween-20 0.5M 100% Tween-20

    500mM NaCl50ml 5M NaCl

    dH2O Fill to 0.5L (start w/ 350ml)

    Sonication and Solubility Test:

    Resuspend 1L worth of bacterial pellet in 30ml Low Buffer

    Take 30μl pre-sonication sample

    Sonicate 3 pulses at 80% power with 7th floor sonicator,2 min on ice between pulses (NOTE: do not let sonicator tip touch side of tube to reduce frothing)

    Take 30μl crude sonicated sample

    Dispense into 1.5 ml eppendorf tubes,spin 14k rpm,4℃,30 min

    Combine soluble fractions into 1 tube

    Take 30μl soluble fraction as post-sonication soluble sample

    Test solubility of target protein by SDS-PAGE/Coomassie Blue Stain

    Add 10μl 4x Sample Buffer and 2μl ?-Mercaptoethanol to each 30μl sample

    Add an equal volume of 4x Sample Buffer to one insoluble pellet,add β-Mercaptoethanol to a final concentration of 5%.

    Load 14μl (equals 10μl of fraction)on an appropriate concentration SDS-PAGE gel,electrophorese to separate bands well

    Stain with Coomassie Blue for 30 min @ RT with rocking,destain with shreds of brown paper towel to aid in removal of dye from gel

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