国产精品久久久久久永久牛牛,55国产福利在线视频,成人午夜精品视频在线观看

目錄產品 » PCR試劑 » Taq DNA Polymerase without Mg2+
Manual
SDS
COAs

Taq DNA Polymerase without Mg2+

DNA Polymerase is a thermostable DNA polymerase isolated from an E. coli strain that carries the Taq DNA polymerase gene. Taq DNA polymerase is the most common polymerase used for PCR.
¥400
E00008

Description

DNA Polymerase is a thermostable DNA polymerase isolated from an E. coli strain that carries the Taq DNA polymerase gene. Taq DNA polymerase is the most common polymerase used for PCR.

Note

Formulation
GenScript Taq DNA Polymerase has been formulated using GenScript's proprietary technology. The enzyme can be shipped at room temperature or even 37°C for seven days without any loss of activity.

Unit Definition
One unit is the amount of enzyme that can incorporate 10 nmol of dNTP into acid-insoluble material in 30 minutes at 74°C.

10 X Reaction Buffer (without Mg2+)
500 mM KCl, 100 mM Tris HCl (pH 9.0 at 25°C), 1% Triton X-100 Buffer. This buffer is optimized for use with 200 μM dNTPs.
Note: If the reaction is performed without this buffer, then add 0.1% Triton X-100 (final concentration) to ensure high activity.
Storage Buffer and Concentration
Taq is delivered in 5 units/μl in 20 mM Tris HCl (pH 8.0), 0.1 mM EDTA, 1 mM DTT, 0.1% Triton X-100 and 50% glycerol.

Storage:
-20°C

*The PCR process is covered by US. Patents numbers 4683195 and 4683202, issued to Cetus and owned by Hoffman-La Roche Inc. GenScript does not encourage or support the unauthorized use of the PCR process. Use of this product is recommended for persons who either have a license to perform PCR or are not required to obtain a license. Sale of this product is restricted to regions or countries where native Taq DNA polymerase patents have been invalidated.

Key Features
  • Terminal transferase activity: Taq DNA Polymerase has terminal transferase activity, which results in the addition of a single nucleotide (adenosine) at the 3' end of the extension product.
  • High purity: No contamination activity has been detected in standard test reactions.
返回

QC
QC Tests
PCR* performance, activity, nuclease

Lane Taq Unit used
1Leading
Brand A
0.1
2 0.25
3 0.5
4Leading
Brand B
0.1
5 0.25
6 0.5
7GenScript0.1
8 0.25
9 0.5


返回

  • PCR*
  • 3' A-tailing of blunt ends
  • Primer extension
  • DNA sequencing

返回

    主站蜘蛛池模板: 磴口县| 香河县| 桂东县| 台江县| 武冈市| 子洲县| 双江| 龙南县| 青铜峡市| 馆陶县| 正镶白旗| 潞城市| 克拉玛依市| 哈巴河县| 吴堡县| 嘉善县| 璧山县| 临洮县| 宜阳县| 恩平市| 清镇市| 谢通门县| 托克托县| 内江市| 枣阳市| 杨浦区| 霍城县| 蒙山县| 谢通门县| 屏东县| 十堰市| 怀远县| 都兰县| 阜宁县| 承德市| 大宁县| 乐亭县| 乌拉特中旗| 金堂县| 抚顺县| 华蓥市|