Primer set and method for amplifying exons of PKD1 gene and PKD2 gene

US10538812B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10538812-B2
Application numberUS-201515534853-A
CountryUS
Kind codeB2
Filing dateNov 13, 2015
Priority dateNov 19, 2014
Publication dateJan 21, 2020
Grant dateJan 21, 2020

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Abstract

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The present invention provides a means for efficiently amplifying the exons of PKD1 and PKD2 genes, and a primer set that can amplify all the exons of PKD1 and PKD2 genes under a single set of PCR conditions.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for amplifying all the exons of PKD1 and PKD2 genes under a single set of PCR cycling conditions, the method comprising performing PCR using a primer set capable of amplifying all the exons of PKD1 and PDK2 genes under a single set of PCR cycling conditions, wherein said primer set comprises the following primer pairs; a first primer pair comprising a 1F primer and a 1R primer, wherein the sequence of the 1F primer comprises a sequence at least 90% identical to the sequence of positions 15 to 29 of the nucleotide sequence of SEQ ID NO: 1, and the sequence of the 1R primer comprises a sequence at least 90% identical to the sequence of positions 16 to 30 of the nucleotide sequence of SEQ ID NO: 2; a second primer pair comprising a 2F primer and a 2R primer, wherein the sequence of the 2F primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 3, and the sequence of the 2R primer comprises a sequence at least 90% identical to the sequence of positions 13 to 27 of the nucleotide sequence of SEQ ID NO: 4; a third primer pair comprising a 3F primer and a 3R primer, wherein the sequence of the 3F primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 5, and the 3R primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 6; a fourth primer pair comprising a 4F primer and a 4R primer, wherein the sequence of the 4F primer comprises a sequence at least 90% identical to the sequence of positions 6 to 20 of the nucleotide sequence of SEQ ID NO: 7, and the 4R primer comprises a sequence at least 90% identical to the sequence of positions 8 to 22 of the nucleotide sequence of SEQ ID NO: 8, a fifth primer pair comprising a 5F primer and a 5R primer, wherein the sequence of the 5F primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 9, and the 5R primer comprises a sequence at least 90% identical to the sequence of positions 10 to 24 of the nucleotide sequence of SEQ ID NO: 10; a sixth primer pair comprising a 6F primer and a 6R primer, wherein the sequence of the 6F primer comprises a sequence at least 90% identical to the sequence of positions 12 to 26 of the nucleotide sequence of SEQ ID NO: 11, and the 6R primer comprises a sequence at least 90% identical to the sequence of positions 12 to 26 of the nucleotide sequence of SEQ ID NO: 12; a seventh primer pair comprising a 7F primer and a 7R primer, wherein the sequence of the 7F primer comprises a sequence at least 90% identical to the sequence of positions 21 to 35 of the nucleotide sequence of SEQ ID NO: 13, and the 7R primer comprises a sequence at least 90% identical to the sequence of positions 20 to 34 of the nucleotide sequence of SEQ ID NO: 14; an eighth primer pair comprising an 8F primer and an 8R primer, wherein the sequence of the 8F primer comprises a sequence at least 90% identical to the sequence of positions 16 to 30 of the nucleotide sequence of SEQ ID NO: 15, and the 8R primer comprises a sequence at least 90%, identical to the sequence of positions 13 to 27 of the nucleotide sequence of SEQ ID NO: 16; a ninth primer pair comprising a 9F primer and a 9R primer, wherein the sequence of the 9F primer comprises a sequence at least 90% identical to the sequence of positions 21 to 35 of the nucleotide sequence of SEQ ID NO: 17, and the 9R primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 18; a tenth primer pair comprising a 10F primer and a 10R primer, wherein the sequence of the 10F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 19, and the 10R primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 20; an eleventh primer pair comprising an 11F primer and an 11R primer, wherein the sequence of the 11F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 21, and the 11R primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 22; a twelfth primer pair comprising a 12F primer and a 12R primer, wherein the sequence of the 12F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 23, and the 12R primer comprises a sequence at least 90% identical to the sequence of positions 17 to 31 of the nucleotide sequence of SEQ ID NO: 24; a thirteenth primer pair comprising a 13F primer and a 13R primer, wherein the sequence of the 13F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 25, and the 13R primer comprises a sequence at least 90% identical to the sequence of positions 16 to 30 of the nucleotide sequence of SEQ ID NO: 26; a fourteenth primer pair comprising a 14F primer and a 14R primer, wherein the sequence of the 14F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 27, and the 14R primer comprises a sequence at least 90% identical to the sequence of positions 12 to 26 of the nucleotide sequence of SEQ ID NO: 28; a fifteenth primer pair comprising a 15F primer and a 15R primer, wherein the sequence of the 15F primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 29, and the 15R primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 30; a sixteenth primer pair comprising a 16F primer and a 16R primer, wherein the sequence of the 16F primer comprises a sequence at least 90% identical to the sequence of positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 31, and the 16R primer comprises a sequence at least 90% identical to the sequence of positions 11 to 25 of the nucleotide sequence of SEQ ID NO: 32; a seventeenth primer pair comprising a 17F primer and a 17R primer, wherein the sequence of the 17F primer comprises a sequence at least 90% identical to the sequence of positions 16 to 30 of the nucleotide sequence of SEQ ID NO: 33, and the 17R primer comprises a sequence at least 90% identical to the sequence of positions 12 to 26 of the nucleotide sequence of SEQ ID NO: 34; and an eighteenth primer pair comprising an 18F primer and an 18R primer, wherein the sequence of the 18F primer comprises a sequence at least 90% identical to the sequence of positions 12 to 26 of the nucleotide sequence of SEQ ID NO: 35, and the 18R primer comprises a sequence at least 90% identical to the sequence of positions 13 to 27 of the nucleotide sequence of SEQ ID NO: 36. 2. The method according to claim 1 , wherein the PCR uses multiple reaction vessels. 3. The method according to claim 2 , wherein the PCR using multiple reaction vessels are all performed simultaneously. 4. The method according to claim 1 , wherein each of the primers has a length of 15 to 40 bases. 5. The method according to claim 1 , wherein the sequence of the 1F primer comprises at least positions 15 to 29 of the nucleotide sequence of SEQ ID NO: 1, and the sequence of the 1R primer comprises at least positions 16 to 30 of the nucleotide sequence of SEQ ID NO: 2; wherein the sequence of the 2F primer comprises at least positions 14 to 28 of the nucleotide sequence of SEQ ID NO: 3, and the sequence of the 2R primer com

Assignees

Inventors

Classifications

  • Recombinant DNA-technology · CPC title

  • involving nucleic acids · CPC title

  • C12Q1/6883Primary

    for diseases caused by alterations of genetic material · CPC title

  • Primer sets for multiplex assays · CPC title

  • Prognosis of disease development · CPC title

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Frequently asked questions

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What does patent US10538812B2 cover?
The present invention provides a means for efficiently amplifying the exons of PKD1 and PKD2 genes, and a primer set that can amplify all the exons of PKD1 and PKD2 genes under a single set of PCR conditions.
Who is the assignee on this patent?
Otsuka Pharma Co Ltd
What technology area does this patent fall under?
Primary CPC classification C12Q1/6883. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 21 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).