推薦產品
形狀
liquid
用途
sufficient for 100 reactions
sufficient for 400 reactions
特點
dNTPs included
hotstart
濃度
1 units/reaction (20 μL reaction volume)
技術
qPCR: suitable
顏色
colorless
輸入
purified DNA
相容性
for use with Roche LightCycler 480
檢測方法
SYBR® Green
運輸包裝
wet ice
儲存溫度
−20°C
一般說明
SYBR Green Taq ReadyMix可用于单个产品实时扩增实验,也可用于评价产生荧光标记探针之前的引物序列。 不建议将荧光标记探针与SYBR Green I染料一起使用。
應用
特點和優勢
- 方便的2×浓缩预混液,专门设计用于毛细管仪器,例如Roche LightCycler®,是高通量应用的理想选择
- 提高特异性&目标产量-JumpStart™ Taq聚合酶可防止非特异性产物,从而获得更准确的CT值并改善定量
- 该预混液可确保反应间一致性
- 缩短了制备时间,并降低了多个移液步骤造成的污染风险
- SYBR® Green I荧光染料特异性结合双链DNA,低价、易用、灵敏,是任意DNA序列定量分析的理想选择
包裝
100RXN包装为1 X 1 mL
400RXN包装为1 X 4 mL
原則
JumpStart Taq抗体在室温下能够使DNA聚合酶失活。当温度在第一步循环变性中升高到70℃以上,复合体解离,聚合酶完全被激活。JumpStart Taq DNA聚合酶防止非特异性扩增,能够获得更为准确的CT值。
为制备反应,将10 μL ReadyMix加入引物、模板和水中,使最终反应体积为20 μL。
單位定義
法律資訊
相關產品
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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文章
qPCR investigates gene expression, amplification, and alterations, crucial for tumor biology and understanding cancer genetics.
Watch these videos to learn how real time or quantitative PCR (qPCR) works and the benefits of both the SYBR Green-based and probe-based methods of qPCR assay.
觀看這些影片,瞭解即時或定量 PCR (qPCR) 的工作原理,以及以 SYBR Green 為基礎和以探針為基礎的 qPCR 分析方法的優點。
The polymerase chain reaction is one of the most widely used techniques in molecular biology. The PCR process consists of three main steps, Denaturation, Annealing & Extension
條款
A protocol that can be used as a basic template for qPCR incorporating SYBR Green I DNA binding dye that is amenable to modification and applicable for use as validation for a set of primers.
Our SYBR Green qPCR Protocol is a method designed to detect accurate quantification of gene expression and RT-PCR reactions
我們的 SYBR Green qPCR 協定是專為檢測基因表達和 RT-PCR 反應的精確定量而設計的方法
相關內容
SYBR® Green I, a commonly used fluorescent DNA binding dye, binds all double-stranded DNA and detection is monitored by measuring the increase in fluorescence throughout the cycle. Explore our LuminoCt® and KiCqStart® products for Fast qPCR or JumpStart™ reagents for conventional qPCR
A protocol that can be used as a basic template for qPCR incorporating SYBR Green I DNA binding dye that is amenable to modification and applicable for use as validation for a set of primers.
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