Primer group and kit for detecting human platelet alloantigen gene
An alloantigen, primer set technology, applied in the biological field
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Embodiment 1
[0079] According to the HPA allele sequence released by the National Center for Biotechnology Information (NCBI Gene Bank), a primer set for detecting the human platelet alloantigen gene was designed. The primer set included HPA-6a primer pair, HPA-6b Primer pair, HPA-15Gov a Primer pair, HPA-15Gov b Primer pairs and internal reference primer pairs.
Embodiment 2
[0081]According to the HPA allele sequence released by the National Center for Biotechnology Information (NCBI Gene Bank), a primer set for detecting the human platelet alloantigen gene was designed, and the primer set included HPA-1a primer pair, HPA-1b Primer pair, HPA-2a primer pair, HPA-2b primer pair, HPA-3a primer pair, HPA-3b primer pair, HPA-4a primer pair, HPA-4b primer pair, HPA-5a primer pair, HPA-5b primer pair , HPA-6a primer pair, HPA-6b primer pair, HPA-15Gov a Primer pair, HPA-15Gov b Primer pair, HPA-7a primer pair, HPA-7b primer pair, HPA-8a primer pair, HPA-8b primer pair, HPA-9a primer pair, HPA-9b primer pair, HPA-10a primer pair, HPA-10b primer pair , HPA-11a primer pair, HPA-11b primer pair, HPA-12a primer pair, HPA-12b primer pair, HPA-13a primer pair, HPA-13b primer pair, HPA-14a primer pair, HPA-14b primer pair, HPA - 16a primer pair, HPA-16b primer pair, HPA-17a primer pair, HPA-17b primer pair and internal reference primer pair.
Embodiment 3
[0083] A kit for detecting human platelet alloantigen gene, comprising a pair of primers coated with HPA-6a, a pair of primers for HPA-6b, a pair of HPA-15Gov a Primer pair, HPA-15Gov b Primer pairs, primer plates for internal reference primer pairs, and enriched dNTP-Buffer,
[0084] The preparation method of the test kit for detecting human platelet alloantigen gene is:
[0085] (1) According to the HPA (1-17) specific primer hole map (see figure 2 ), HPA-6a primer pair, HPA-6b primer pair, HPA-15Gov a Primer pair, HPA-15Gov b The primer pair and the internal reference primer pair are coated on the corresponding positions of the primer plate and dried;
[0086] (2) According to the formula 200mM dNTP, 3.5mM Mg 2+ , 500mM KCL, 100mM Tris-HCL, 1% TritonX-100, prepared 440μl concentrated dNTP-Buffer;
[0087] (3) The primer plate coated with the primer pair and the concentrated dNTP-Buffer are used to form a kit for detecting human platelet alloantigen gene.
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