A kind of phosphorylated eif5b specific antibody and its preparation method and application
A specific and phosphorylation technology, applied in chemical instruments and methods, antibodies, anti-receptor/cell surface antigen/cell surface determinant immunoglobulin, etc., can solve the problems of few types of EIF5B antibodies and poor specificity
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[0034] This embodiment provides a phosphorylated EIF5B-specific antibody, specifically, the antibody is a polyclonal antibody specific to human phosphorylated EIF5BT78.
[0035] Phosphorylated ElF5B T78 specific site polyclonal antibody was prepared by the following method:
[0036] S1. Prepare the antigen. First, synthesize 20 mg of polypeptide 1 according to the protein sequence of EIF5B (as shown in SEQ ID NO: 3). The amino acid sequence of the polypeptide 1 is as shown in SEQ ID NO: 1: KADRET(p)VAVKPTENN-Cys, In SEQ ID NO: 1, threochloric acid (T) at this site is phosphorylated. Take 10 mg of polypeptide 1 coupled with hemocyanin (KLH) to prepare the antigen. The mass spectrometry results of polypeptide 1 and the polypeptide coupled with KLH are as follows: Figure 1-2 shown.
[0037] S2. Prepare an antibody, and immunize the polypeptide 1 coupled with hemocyanin as an antigen to obtain an antibody. Two New Zealand white rabbits were immunized with KLH-coupled polypept...
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[0109] 1. Antibody endogenous verification
[0110] Western Blot (WB) verification:
[0111] The main instruments used are shown in Table 2 below:
[0112] Table 2
[0113]
[0114] The main reagents used are shown in Table 3 below:
[0115] table 3
[0116]
[0117] The detection process specifically includes the following steps:
[0118] Sample preparation: Use A549 and 143B cells to prepare phosphorylated EIF5B activated cell samples, collect the cells, use RIPA lysate ((RIPA Lysis Buffer)) to lyse the cells at 4°C, and lyse the cells at 4°C at a speed of 12000rpm Centrifuge for 20min and transfer the supernatant to a new EP tube. The protein concentration was determined by BCA method, and 5×SDS loading buffer was added according to the volume of the lysate, and boiled at 100°C for 5 minutes. To prevent protein degradation, operations should be performed on ice as much as possible.
[0119] SDS-PAGE electrophoresis (polyacrylamide gel electrophoresis): clamp th...
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