形狀
buffered aqueous glycerol solution
濃度
10,000 units/mL
運輸包裝
wet ice
儲存溫度
−20°C
特異性
Recognition sequence: 5′-ATTT/AAAT-3′
Ligation and recutting results: After 2-10-fold Swa I overdigestion of 1 μg λ DNA substrate, results in 100% cutting, >95% of fragments can be ligated, and >95% recut.
Heat inactivation: Inactivated at 65 °C for 20 minutes.
Ligation and recutting results: After 2-10-fold Swa I overdigestion of 1 μg λ DNA substrate, results in 100% cutting, >95% of fragments can be ligated, and >95% recut.
Heat inactivation: Inactivated at 65 °C for 20 minutes.
其他說明
Supplied with 10x Restriction Endonuclease Buffer SH (B3657).
外觀
Solution in 20 mM Tris-HCl, pH 8.0, 0.1 mM EDTA, 500 mM NaCl, 10 mM 2-mercaptoethanol, 50% glycerol (v/v) at 4 °C
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Current next-generation sequencing (NGS) platforms adopt two types of sequencing mechanisms: by synthesis or by ligation. The former is employed by 454 and Solexa systems, while the latter by SOLiD system. Although the pros and cons for each sequencing mechanism
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