2×GoldStar MasterMix (Dye),货号-规格:CW0960M-5ml
市场价: | ¥598.0 | |||||||||||||||||||
价格: |
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品牌: | 康为世纪 | |||||||||||||||||||
规格: | 5ml |
产品详情
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参考文献
2×GoldStar MasterMix (Dye),货号-规格:CW0960M-5ml 2×GoldStar MasterMix是由GoldStar DNA Polymerase、PCR Buffer、Mg2+、dNTPs及PCR稳定剂和增强剂组成的预混体系,预混好的PCR混合液使操作更加简单快捷,可最大限度地减少人为误差和污染。该产品所含有的GoldStar DNA Poly- merase是一种经化学修饰的、全新高效Taq DNA Polymerase,在常温下酶的活性被完全封闭,使得该酶在低温或常温下没有活性,从而有效避免在常温条件下由引物和模板非特异性结合或引物二聚体而产生的非特异性扩增,酶的激活须在95℃下孵育10分钟。独特的缓冲体系使酶的应用更为广泛,使GC含量高、二级结构复杂以及低拷贝的模板,均能高效扩增,特有的MasterMix配方使整个反应体系稳定性更强。本产品已加入染料(蓝色),反应结束后可直接进行电泳检测。用本品进行PCR扩增,PCR产物3'末端附有一个“A”碱基,可直接用于T/A克隆。本产品特异性强,PCR扩增后无需胶回收去除杂带,可直接用于下游克隆或芯片杂交等实验。主要应用于常规的PCR、RT-PCR和多重PCR,特别适用于对特异性要求较高的PCR反应。 2xGoldStar MasterMix (Dye) 立即下载 |
Gel Loading Dye, Blue (6X) |NEB酶试剂 New England Biolabs
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
Gel Loading Dye, Blue (6X)
Gel Loading Dye, Blue (6X) is a Bromophenol Blue-based loading dye offering convenient gel loading and sharp bands.
- For use with agarose and non-denaturing polyacrilamide gels
- Contains SDS for improved band sharpness
- Contains EDTA to halt enzymatic reactions
You may also be interested in our Gel Loading Dye, Purple (6X) with and without SDS, for sharp bands and no UV shadow.
Gel Loading Dye, Orange (6X) |NEB酶试剂 New England Biolabs
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
Gel Loading Dye, Orange (6X)
Gel Loading Dye, Orange (6X) is an Orange G-based loading dye for convenient gel loading and sharp bands
- For use with agarose and non-denaturing polyacrylamide gels
- Contains SDS for improved band sharpness
- Contains EDTA to stop enzymatic reactions
- Orange G will not appear in gel photographs
- You may also be interested in our Gel Loading Dye, Purple (6X) with and without SDS, for sharp bands and no UV shadow.
RNA Loading Dye, (2X) |NEB酶试剂 New England Biolabs
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
RNA Loading Dye, (2X)
- 2X pre-mixed loading dye for use with denaturing and non-denaturing gels
- Free from detectable endonuclease, exonuclease and RNase activities