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A kind of multi-label antigen and its preparation method and application

A multi-label and labeling technology, applied in the field of western blotting, can solve the problems of increased detection cost, time-consuming and laborious, etc., and achieve the effects of saving detection cost, good compatibility, and strong specificity of Western blotting reaction

Active Publication Date: 2018-06-05
YEASEN BIOTECHNOLOGY (SHANGHAI) CO LTD
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Commonly used tags include GST tag, HA tag, StrepII tag, Flag tag, EGFP tag, and His tag. In protein detection, different target proteins often choose different tag sequences according to their properties. In the prior art, many A single tag is used as a positive control, so when multiple proteins to be tested contain multiple different tag sequences, multiple corresponding positive controls are required, which is time-consuming and laborious, and increases the detection cost

Method used

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  • A kind of multi-label antigen and its preparation method and application
  • A kind of multi-label antigen and its preparation method and application
  • A kind of multi-label antigen and its preparation method and application

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Embodiment Construction

[0023] The technical solutions of the present invention will be further described below through specific examples. The following examples are to further illustrate the present invention, but not to limit the scope of the present invention.

[0024] 1. MultiTag-G9 artificial gene synthesis

[0025] MultiTag-G9 contains 9 common detection tags, namely GST, HA, T7, V5, Myc, StrepII, Flag, EGFP and His tags. The specific DNA sequences are:

[0026] GST label

[0027]

[0028] HA tag

[0029] tatccgtatg atgttccgga ttatgca 27

[0030] T7 label

[0031] atggcatcaa tgacaggcgg ccagcagatg ggc 33

[0032] V5 label

[0033] ggcaaaccga ttccgaatcc gctgctgggc ctggattcaa ca 42

[0034] Myc Tags

[0035] gaacagaaac tgatttcaga agaagatctg 30

[0036] Strep II label

[0037] tggtcacatc cgcagtttga aaaa 24

[0038] Flag tag

[0039] gattataaag atgatgatga taaa 24

[0040] EGFP tag

[0041]

[0042]

[0043] His tag

[0044] catcatcatc atcatcat 18

[0045] The above nine tag...

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Abstract

The invention discloses a multi-tag antigen. The multi-tag antigen comprises the following nine tags: a GST tag, an HA tag, a T7 tag, a V5 tag, a Myc tag, a StrepII tag, a Flag tag, an EGFP tag and a His tag which are connected in series according to a sequence of GST-HA-T7-V5-Myc-StrepII-Flag-EGFP-His. The invention also discloses a preparation method for the multi-tag antigen and application of the multi-tag antigen in immunoblotting. The multi-tag antigen disclosed in the invention can meet demand for setting of positive contrast in most immunoblotting reactions and has good compatibility and strong immunoblotting specificity.

Description

technical field [0001] The invention relates to the field of immunoblotting, in particular to a multi-label antigen and its preparation method and application. Background technique [0002] Western blotting is a technique in which proteins are transferred to a membrane and then detected using antibodies. For the known expressed protein, the corresponding antibody can be used as the primary antibody for detection, and for the expression product of the new gene, it can be detected by the antibody of the fusion part, which has the advantages of large analysis capacity, high sensitivity, and strong specificity. One of the most commonly used methods of expression and distribution, such as the qualitative and quantitative detection of tissue antigens, the mass determination of polypeptide molecules, and the detection of virus antibodies or antigens, etc., so Western blotting technology has a wide range of applications in molecular biology research. [0003] When designing and exp...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/11C12N15/70G01N33/68C12R1/19
Inventor 曹平生
Owner YEASEN BIOTECHNOLOGY (SHANGHAI) CO LTD
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