# US 8,785,126 B2 · Methods for the reduction of stutter in microsatellite amplification > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 8,785,126 B2 - Document ID: US8785126B2 - Status: Granted - Kind: B2 - Application number: 13/611,974 - Filed: 2012-09-12 - Published: 2013-01-10 - Granted: 2014-07-22 - Earliest claimed: 2001-05-07 - Assignees: Applied Biosystems, LLC - Applicants: Sulekha Rao Coticone; William Bloch - Inventors: Sulekha Rao Coticone; William Bloch - Web page: https://patentgrep.com/patent/US8785126B2 ## CPC - C12Q 1/686: Polymerase chain reaction [PCR] - C12Q 1/6848: characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction - C12Q 1/6846: {Common amplification features} - C12Q 1/6876: Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes - C12Q: MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES ## Abstract The invention provides a method for reducing stutter in the amplification of a microsatellite comprising the steps of providing a sample comprising a microsatellite having a G+C content of 50% or less; contacting the sample with at least one enzyme having nucleic acid polymerase activity; and incubating the sample with the enzyme for a sufficient amount of time and under conditions sufficient to amplify the microsatellite; wherein the incubation is performed in the presence of an amount of betaine, sorbitol or mixtures thereof, effective to reduce stutter relative to the amount of stutter observed in the absence of betaine and/or sorbitol. The invention also provides compositions containing betaine and/or sorbitol, kits for amplifying microsatellites having a G+C content of 50% or less, and methods of using all of the foregoing. ## Claims ### Claim 1 A method of personal genetic identification comprising amplifying a plurality of regions of DNA from a sample containing DNA from a subject, wherein said regions comprise at least one microsatellite selected from the group consisting of a tetranucleotide repeat and a pentanucleotide repeat, wherein said microsatellite has a G+C content of 50% or less, wherein said amplification comprises the steps of: (a) contacting said DNA with at least one enzyme having nucleic acid polymerase activity; (b) incubating said sample with said enzyme for a time and under conditions sufficient to amplify said regions; (c) separating said amplified regions, forming a microsatellite pattern; and (d) comparing said microsatellite pattern with a corresponding microsatellite pattern derived from a DNA sample from a second source; wherein said incubation is performed in the presence of an amount of an additive selected from the group consisting of sorbitol, betaine and mixtures thereof, wherein said additive is effective to reduce the amount of stutter arising from said amplification relative to the amount of such stutter observed in the absence of said additive. ### Claim 2 (depends on 1) The method of claim 1 wherein said incubation is performed in the presence of a set of dNTPs, said set comprising a first dNTP corresponding to dATP, a second dNTP corresponding to dGTP, a third dNTP corresponding to dCTP, and a fourth dNTP corresponding to dTTP; wherein each of said dNTP is present at a concentration of at least 0.5 mM. ### Claim 3 (depends on 1) The method of claim 1 wherein said additive is present at a concentration of 1.5 to 3.5 M. ### Claim 4 (depends on 1) The method of claim 1 wherein said additive is present at a concentration of 2.0 to 3.0 M. ### Claim 5 (depends on 2) The method of claim 2 wherein each of said dNTPs is present at a concentration of 0.5 mM to about 2.0 mM. ### Claim 6 (depends on 5) The method of claim 5 wherein each of said dNTPs is present at a concentration from about 1.0 mM to about 2.0 mM. ### Claim 7 (depends on 1) The method of claim 1 wherein the additive is betaine. ### Claim 8 (depends on 1) The method of claim 1 wherein the additive is sorbitol. ### Claim 9 (depends on 1) The method of claim 1 wherein the sample is a forsensic sample. ### Claim 10 (depends on 9) The method of claim 9 wherein said second source comprises at least one selected from the group consisting of the presumed matching source, a family member of the presumed matching source, and a database of sources. ### Claim 11 (depends on 1) The method of claim 1 wherein said regions of DNA comprise at least one genetic locus selected from the group consisting of D3S1358, VWA, D16S539, D8S1179, D21S11, D18S51, D19S433, TH01, FGA, D7S820, D13S317, D5S818, CSF1PO, TPOX, CD4, CYAR04, F13A01, F13B, FABP, FES/FPS, HPRTB, LPL, Penta D, Penta E, PLA2A1, D1S1656, D2S1242, D3S1359, D3S1744, D6S477, D8S347, D8S639, D9S302, D10S2325, D11S488, D11S554, D12S391, D12S1090, D18S535, D18S849, D20S161, D22S683, DXS6807, D19S433, and D10S2325. ### Claim 12 (depends on 1) The method of claim 1 wherein said subject is human, bovine, dog, or horse. ### Claim 13 (depends on 1) The method of claim 1 wherein said stutter is reduced to 60% or less than the amount of stutter obtained in the absence of said additive. ### Claim 14 (depends on 1) The method of claim 1 wherein said stutter is reduced to 50% or less than the amount of stutter obtained in the absence of said additive. ### Claim 15 (depends on 1) The method of claim 1 wherein the polymerase is selected from the group consisting of Taq DNA polymerase, Tth DNA polymerase, Tne Bst DNA polymerase large fragment from Bacillus stearothennophilus, DNA polymerase from Thermococcus litoralis, Tma from Thennotoga maritiama, and Pfu from Pyrococcus.