Taq DNA polymerase monoclonal antibody combination, polymerase reaction system containing same and application of Taq DNA polymerase monoclonal antibody combination

A monoclonal antibody and reaction system technology, applied in the direction of anti-enzyme immunoglobulin, microbial determination/testing, biochemical equipment and methods, etc., can solve the long-term stability of enzymes, the decline of amplification ability, and the time-consuming antibody screening Energy consumption and other issues, to achieve the effect of maintaining persistence, ensuring thermal stability, and protecting the activity of TaqDNA polymerase

Active Publication Date: 2020-09-15
BEIJING TRANSGEN BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] However, due to the time-consuming and labor-intensive antibody screening, it is difficult to screen for the best antibody. Although non-specific amplification can be reduced to a certain extent, the inc

Method used

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  • Taq DNA polymerase monoclonal antibody combination, polymerase reaction system containing same and application of Taq DNA polymerase monoclonal antibody combination
  • Taq DNA polymerase monoclonal antibody combination, polymerase reaction system containing same and application of Taq DNA polymerase monoclonal antibody combination
  • Taq DNA polymerase monoclonal antibody combination, polymerase reaction system containing same and application of Taq DNA polymerase monoclonal antibody combination

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0073] Example 1 Animal immunization, fusion and preliminary screening process

[0074] (1) Animal immunity:

[0075] Eight-week-old BALB / C female mice were used, the antigen was EasyTaq DNA polymerase, and the conventional immunization method was used for immunization. The specific immunization method:

[0076] For the first immunization, the immunogen obtained by subcutaneously injecting 50 μg of EasyTaq DNA polymerase and Freund’s complete adjuvant in equal volumes was injected subcutaneously at 3 to 4 points on the back of each mouse;

[0077] Two weeks later, the second immunization was carried out, and the immunogen obtained by subcutaneously injecting 50 μg of EasyTaq DNA polymerase and Freund’s incomplete adjuvant in equal volumes was injected subcutaneously at 3 to 4 points on the back of each mouse;

[0078] Three immunizations were carried out two weeks later, and the immunogen obtained by mixing equal volumes of 50 μg EasyTaq DNA polymerase and Freund's incomplete...

Embodiment 2

[0093] Embodiment 2 Expansion inhibition screening of hybridoma cells

[0094] In order to detect whether the antibody secreted by the initially screened hybridoma cell line has the effect of blocking the active region of EasyTaq DNA polymerase, the molecular beacon detection experiment is used for verification. The principle of the molecular beacon detection experiment is as follows: figure 1 As shown, the primer is complementary to the loop region of Molecular Beacon (MB, whose sequence is shown in SEQ ID NO.7), and after extension, the stem-loop of MB can be opened, resulting in luminescence. A stem-loop primer (ie Primer-MB shown in SEQ ID NO.8) was designed according to Molecular Beacon.

[0095] (1) Use 10×Reaction Buffer in EasyTaq DNA polymerase (TransGen, AP111) as the reaction solution, and prepare the reaction system in the PCR tube according to the following system:

[0096]

[0097] (2) Using a BioRad CFX96 fluorescent quantitative PCR instrument, incubate at...

Embodiment 3

[0104] Embodiment 3 Gene amplification and subtype identification of hybridoma cells

[0105] Primers were designed through the signal peptide sequences and constant regions on the heavy chain and light chain of the antibody secreted by hybridoma cells, and the total RNA of hybridoma cells was extracted and reverse-transcribed into cDNA. Using the cDNA as a template, VH-VDJ-UmIgVH+( SEQ ID NO.9) and VH-VDJ-UmIgJH-(SEQ ID NO.10) amplified to obtain antibody heavy chain variable region (V H ) DNA sequence, using VL-VDJ-UmIgVK+ (SEQ ID NO.11) and VL-VDJ-UmIgJK- (SEQ ID NO.12) to amplify the antibody light chain variable region (V L ) DNA sequence.

[0106] Use 2×TransStart FastPfu Fly PCR SuperMix for amplification, and prepare the reaction system in the PCR tube according to the following system.

[0107]

[0108] Use a pipette or vortex to mix thoroughly, place the PCR tube in the PCR machine and perform the following procedures:

[0109]

[0110] The DNA sequences of ...

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Abstract

The invention discloses a Taq DNA polymerase monoclonal antibody combination, a polymerase reaction system containing the same and application of the Taq DNA polymerase monoclonal antibody combination. The invention firstly discloses the Taq DNA polymerase monoclonal antibody combination, and the combination comprises a monoclonal antibody 4A8 and a monoclonal antibody 5H6. The invention further discloses application of the antibody combination in reducing non-specific amplification of Taq DNA polymerase and/or ensuring the thermal stability of the Taq DNA polymerase, the reaction system containing the combination, and a kit. The antibody combination and an optimized reaction solution can fully seal an active region of the Taq DNA polymerase under the condition of low temperature, effectively reduce non-specific amplification and ensure the thermal stability of the enzyme, and can still effectively maintain the durability of the enzyme activity under the condition of higher cycle number of amplification.

Description

technical field [0001] The present invention relates to the field of biotechnology. More specifically, it relates to a Taq DNA polymerase monoclonal antibody combination, a polymerase reaction system containing it, and applications thereof. Background technique [0002] Polymerase chain reaction (polymerase chain reaction, PCR) technology is widely used in molecular biology experiments, a DNA molecule can be amplified 10 times in a few hours in vitro 9 times. PCR technology is similar to the natural replication process of double-stranded DNA. Under the catalysis of DNA polymerase, the mother-strand DNA is used as the template, and the specific primer is used as the starting point of extension. Through steps such as denaturation, annealing, and extension, the DNA of the parent-strand template is replicated in vitro. Complementary daughter strand DNA process. DNA polymerase is the key to DNA replication. [0003] Taq DNA polymerase is a thermostable DNA polymerase isolated...

Claims

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Application Information

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IPC IPC(8): C07K16/40C12Q1/6848
CPCC07K16/40C07K2317/56C07K2317/565C12Q1/6848C12Q2527/125C12Q2549/101C12Q2521/101C12Q2531/113
Inventor 曹洋李行宋新文张帅耿亮马静辛文
Owner BEIJING TRANSGEN BIOTECH CO LTD
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