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    OVERVIEW

    In addition to the typical main application, the polymerase chain reaction (PCR), the Biometra TRobot II

    is also suitable for all other molecular biological or chemical incubations in PCR plates. For example,

    the generation of libraries for Next Generation Sequencing (NGS) is an important step in a larger workflow where the automated thermal cycler can be used. This reduces the manual effort and the possibility of errors.

    The PCR cycler has outstanding heating and cooling rates and excellent temperature homogeneity across

    the sample block for highly reproducible PCR results. For the setup of new protocols or for the transfer

    of existing protocols from other thermal cyclers it is sometimes necessary to make slight optimizations to the protocols.

    For this purpose the Biometra TRobot II includes a gradient function.

    With this function it is possible, to test different temperatures in the critical annealing step of the PCR in one run.

    Read more > 
    122601 Biometra TRobot II Series Media/Uploads/4_optimized(1).png Biometra TRobot II Series <p style="font-size: 19.0008px;"><span style="color: rgb(37, 128, 194); font-size: 36px; font-family: &quot;MS Sans Serif&quot;; font-weight: 700; letter-spacing: 2px;">OVERVIEW</span></p><p style="font-size: 19.0008px;"><span style="color: rgb(0, 0, 0); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;"><span style="color: rgb(52, 52, 52); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;">In addition to the typical main application, the polymerase chain reaction (PCR), the Biometra TRobot II</span></span></p><p style="font-size: 19.0008px;"><span style="color: rgb(0, 0, 0); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;"><span style="color: rgb(52, 52, 52); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;"> is also suitable for all other molecular biological or chemical incubations in PCR plates. For example, </span></span></p><p style="font-size: 19.0008px;"><span style="color: rgb(0, 0, 0); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;"><span style="color: rgb(52, 52, 52); background-color: rgb(255, 255, 255); font-size: 16px; font-family: &quot;Segoe UI&quot;;">the generation of libraries for Next Generation Sequencing (NGS) is an important step in a larger workflow where the automated&nbsp;</span></span><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;">thermal cycler can be used. This reduces the manual effort and the possibility of errors. </span></p><p style="font-size: 19.0008px;"><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;">The PCR cycler has outstanding heating and cooling rates and excellent temperature homogeneity across </span></p><p style="font-size: 19.0008px;"><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;">the sample block for highly reproducible PCR results. For the setup of new protocols or for the transfer </span></p><p style="font-size: 19.0008px;"><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;">of existing protocols from other thermal cyclers it is sometimes necessary to make slight optimizations to the protocols.</span></p><p style="font-size: 19.0008px;"><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;"> For this purpose the Biometra TRobot II includes a gradient function. </span></p><p style="font-size: 19.0008px;"><span style="background-color: rgb(255, 255, 255); color: rgb(52, 52, 52); font-family: &quot;Segoe UI&quot;; font-size: 16px;">With this function it is possible, to test different temperatures in the critical annealing step of the PCR in one run.</span></p> 0.00 0.00 page_29382 0 0 0
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