Anti-human CD45RA rat immune globulin variable region gene and application
An immunoglobulin, variable technology, applied in anti-animal/human immunoglobulin, anti-receptor/cell surface antigen/cell surface determinant immunoglobulin, genetic engineering, etc.
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Embodiment 1
[0023] Nucleotide sequence and amino acid sequence of two genes of the present invention:
[0024] 1. Anti-human CD45RA mouse immunoglobulin heavy chain variable region gene (mAb ZCH-6-3A4VH 3A4 ) nucleotide sequence (SEQ ID NO 1) and amino acid sequence (SEQ ID NO 3).
[0025] 2. Anti-human CD45RA mouse immunoglobulin light chain variable region gene (mAb ZCH-6-3A4VL 3A4 ) nucleotide sequence (SEQ ID NO 2) and amino acid sequence (SEQ ID NO 4).
Embodiment 2
[0027] The ability of 3A4 to recognize antigen and its blocking effect on BD company's anti-CD45RA monoclonal antibody (clone name L48) were detected by flow cytometry inter-standard method ( figure 1 ), 1B in the figure is the flow cytometry diagram of the reaction between 3A4 and KG1a cell line, 1C is the flow diagram of the comparison with the anti-CD45RA monoclonal antibody of BD Company, and 1D is the flow diagram of the blocking experiment of 3A4 anti-CD45RA antibody. The results showed that the positive rate of 3A4 and KG1a cell reaction was 99.51%, and the MFI was 432.63, indicating that the activity of 3A4 antibody was good. figure 1 Peak 1 in E is the negative control, peak 2 is the image after blocking, and peak 3 is the image without blocking, indicating that 3A4 can completely block the reaction between BD’s anti-CD45RA antibody and KG1a, suggesting that the anti-CD45RA antibody and 3A4 recognize the same antigenic epitope.
[0028] Proceed as follows:
[0029] ...
Embodiment 3
[0036] Identification of 3A4 immunoglobulin subclasses: using flow cytometer inter-standard method, KG1a cell line as the reaction cell, 3A4 as the primary antibody, immunoglobulin subclass identification kit as the secondary antibody, and the detection of different immunoglobulins as the secondary antibody Anti-time positive rate and mean fluorescence intensity, see figure 2 , figure 2 In order to adopt the flow cytometry inter-standard method, KG1a cell line was used as the reaction cell, 3A4 was used as the primary antibody, and FITC-labeled goat anti-mouse immunoglobulin subclass antibody was used as the secondary antibody. The positive rate and average of different secondary antibodies were detected. Fluorescence intensity (MFI). The results showed that when IgG1 FITC was used as the secondary antibody, the positive rate was 98.48%, and the MFI was 332.85. When Kappa FITC was used as the secondary antibody, the positive rate was 99.02%, and the MFI was 252.20, indicati...
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