Specific primers and liquid phase chip for polymorphic detection of human hedgehog interacting protein (HHIP) gene
A gene polymorphism and detection solution technology, applied in the field of molecular biology, can solve the problems of high false positive rate, failure to meet the needs of practical applications, detection throughput that cannot meet clinical needs, etc., and achieve low cross-reaction rate Effect
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Embodiment 1
[0021] Embodiment 1 HHIP gene polymorphism detection liquid chip mainly includes:
[0022] 1. ASPE Primers
[0023] Specific primer sequences were designed for wild type and mutant type of two common genotypes T149C and T61C of HHIP gene. Among them, the ASPE primer consists of "Tag sequence + specific primer sequence". ASPE primer sequences are shown in the table below:
[0024] The ASPE primer sequence (Tag sequence+specific primer sequence) of table 1HHIP gene
[0025]
[0026] Each ASPE primer includes two parts, the 5' end is a specific tag sequence for the anti-tag sequence on the corresponding microsphere, and the 3' end is a mutant or wild-type specific primer fragment (as shown in the above table 1). All ASPE primers were synthesized by Shanghai Sangon Bioengineering Technology Service Co., Ltd. Each synthesized primer was prepared into a stock solution of 100 pmol / mL with 10 mmol / L Tris Buffer.
[0027] 2. Microspheres coated with anti-tag sequences
[0028]...
Embodiment 2
[0038] Example 2 Detection of samples using HHIP gene detection liquid chip
[0039] The formula of described various solutions is as follows:
[0040] 50mM MES buffer (pH5.0) formula (250ml):
[0041]
[0042] 2×Tm hybridization buffer
[0043] Reagent
source
Final concentration
Dosage per 250ml
1M Tris-HCl, pH8.0
SigmaT3038
0.2M
50ml
5M NaCl
Sigma S5150
0.4M
20ml
Triton X-100
Sigma T8787
0.16%
0.4ml
[0044] Store at 4°C after filtration.
[0045] ExoSAP-IT kit was purchased from US USB Company.
[0046] Biotin-labeled dCTP was purchased from Shanghai Sangon Bioengineering Technology Service Co., Ltd.
[0047] 1. Sample DNA extraction:
[0048] Refer to the relevant methods of DNA extraction in "Molecular Cloning" to obtain the DNA to be detected.
[0049] 2. PCR amplification of samples to be tested
[0050] Two pairs of primers were designed, and multiplex PCR was us...
Embodiment 3
[0091] The liquid phase chip of embodiment 3 different ASPE primers is to the detection of HHIP gene polymorphic site
[0092] 1. Design of liquid phase chip preparation (selection of Tag sequence and Anti-Tag sequence)
[0093] Taking the HHIP gene T149C site mutation detection liquid chip as an example, the specific primer sequence of the 3' end of the ASPE primer was designed for the wild type and mutant type of T149C, and the Tag sequence at the 5' end of the ASPE primer was selected from SEQ ID NO.1 -SEQ ID NO.4, correspondingly, the anti-tag sequence coated on the microsphere and complementary to the corresponding tag sequence is selected from SEQ ID NO.9-SEQ ID NO.12. The specific design is shown in the following table (Table 7). The synthesis of ASPE primers, microspheres coated with anti-tag sequences, amplification primers, detection methods, etc. are as described in Example 1 and Example 2.
[0094] Table 7 Design of liquid phase chip preparation
[0095]
[0...
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