<div class="page-header with-image bleed">
            <picture>
            <img src="https://surzyme.cn/wp-content/uploads/2026/10/1791772532-1726304239900974.png" width="1920" height="400" class="feature-image wp-post-image" alt="" decoding="async" fetchpriority="high">
        </picture>
        <header class="post-header">
        <h1 class="post-title" style="">Bst DNA Polymerase,Large Fragment</h1>
        <div class="post-metas">
                            <span>Last updated on 2026-10-12</span>
                                    <a href="https://surzyme.cn/author/surzyme/">
                    <span class="meta-author">
                        <img alt='surzyme' src='https://weavatar.com/avatar/af42555338bd02899f2f4c80494cf4fc9a3a807f2521d66cbd4749b27b995a25?s=24&#038;d=mm&#038;r=g' srcset='https://weavatar.com/avatar/af42555338bd02899f2f4c80494cf4fc9a3a807f2521d66cbd4749b27b995a25?s=48&#038;d=mm&#038;r=g 2x' class='avatar avatar-24 photo avatar-small' height='24' width='24' loading='lazy' decoding='async'/>                        surzyme                    </span>
                </a>
                                <span>0 views</span>
                            </div>
    </header>
</div>

<p class="wp-block-paragraph"><strong>Bst DNA Polymerase (Large Fragment)</strong></p>



<p class="wp-block-paragraph"><strong>Summary：</strong></p>



<p class="wp-block-paragraph">Bst DNA Polymerase (Large Fragment) is a truncated portion of Bacillus stearothermophilus DNA polymerase, with 5'→3' DNA polymerase activity but lacking 5'→3' exonuclease activity, and strong strand displacement activity; purity &gt;99%.</p>



<p class="wp-block-paragraph"><strong>Usage：</strong></p>



<p class="wp-block-paragraph">This product is suitable for DNA isothermal amplification, DNA sequencing of GC-rich regions, rapid sequencing of nanogram-level DNA templates, and can be used in experiments requiring mesophilic strand displacement, such as LAMP (loop-mediated isothermal amplification), SDA (strand displacement amplification), NEAR (nicking enzyme isothermal amplification), and other isothermal amplification technologies.</p>



<p class="wp-block-paragraph"><strong>Product Components:</strong></p>



<figure class="wp-block-table"><table class="has-fixed-layout"><tbody><tr><td><strong>Component</strong></td><td><strong>800U &nbsp;8KU</strong></td></tr><tr><td>Bst DNA Polymerase (Large Fragment) (8 U/μL)</td><td>100μL 1 ml</td></tr><tr><td>10×Buffer 1.0</td><td>200μL 2×1 ml</td></tr><tr><td>100mM MgSO4</td><td>200μL 2×1 ml</td></tr></tbody></table></figure>



<p class="wp-block-paragraph"><strong>Storage solution:</strong></p>



<p class="wp-block-paragraph">Enzyme is stored in: 20 mM Tris-HCl, 100 mM KCl, 0.1 mM EDTA, 1 mM DTT, 0.1% Tween20, 50% glycerol, pH 7.5, 25°C.</p>



<p class="wp-block-paragraph">10×Buffer 1.0: 200 mM Tris-HCl pH 8.8 @ 25°C, 100 mM (NH4)2SO4, 1 M KCl, 20 mM MgSO4, 1% Tween 20.</p>



<p class="wp-block-paragraph"><strong>From：</strong></p>



<p class="wp-block-paragraph">This product is derived from an <em>E. coli</em> strain. Using recombinant site-directed mutagenesis technology, the Bacillus stearothermophilus DNA polymerase gene (retaining only the 5'→3' DNA polymerase domain of the gene and lacking its 5'→3' exonuclease domain) was heterologously expressed in an E. coli strain and obtained after purification.</p>



<p class="wp-block-paragraph"><strong>Storage conditions:</strong> Store at -20°C.</p>



<p class="wp-block-paragraph"><strong>Heat inactivation:</strong> Inactivate at 80°C for 20 minutes.</p>



<p class="wp-block-paragraph"><strong>Precautions for use:</strong> It is recommended that the reaction temperature not exceed 70°C. Not suitable for thermal cycling sequencing or PCR.</p>



<p class="wp-block-paragraph">Note: This product is for research use only. Do not use for pharmaceutical, clinical treatment, food, or cosmetic purposes.</p>
