Method for separating proteins by capillary electrophoresis and buffer compositions for capillary electrophoresis
A technology of capillary electrophoresis and protein, applied in the direction of material analysis by electromagnetic means, peptide preparation methods, chemical instruments and methods, etc., can solve the unsatisfactory problems of globulin
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Embodiment 1
[0062] Embodiment 1 (comparison)
[0063] The glycine buffer system was prepared as described above. Normal serum was analyzed.
[0064] Electrophoresis was performed using Method A above.
[0065] from figure 1 It can be seen that the obtained electrophoretic spectrum presents 5 continuous peaks, which are read from left to right and belong to γ, β, α respectively. 2 、α 1 Globulin and albumin components.
Embodiment 2
[0067] Octylate was added to the buffer system of Example 1 at a concentration of 2.5 mM.
[0068] Electrophoresis was performed as described in Example 1.
[0069] from figure 2 It can be seen that the obtained electrophoretic spectrum presents five continuous peaks, belonging to γ, β, α 2 、α 1 Globulin and albumin components. After comparing with the result of Example 1, it is shown that in two components-α 1 Separation between globulin and albumin was greatly improved and return to baseline was improved.
Embodiment 3
[0070] Embodiment 3 (comparison)
[0071] According to the steps of Example 1, the buffer system is the borate buffer solution prepared as described above.
[0072] Electrophoresis was performed as described in Example 1.
[0073] from image 3 It can be seen that the obtained electrophoretic spectrum presents 6 continuous peaks, which belong to γ and β respectively. 2 , β 1 、α 2 、α 1 Globulin and albumin components.
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