推薦產品
形狀
liquid
用途
sufficient for 1250 reactions
sufficient for 250 reactions
sufficient for 5000 reactions
特點
dNTPs included
hotstart
儲存條件
protect from light
技術
qPCR: suitable
顏色
colorless
輸入
purified DNA
相容性
for use with ABI 7500 Fast
for use with ABI 7500
for use with ABI ViiA 7
for use with Agilent AriaMx
for use with Douglas Scientific IntelliQube
for use with Qiagen Rotor-Gene Q
for use with QuantStudio™
for use with Strategene Mx3000P
for use with Strategene Mx3005P
for use with Strategene Mx4000
檢測方法
SYBR® Green
運輸包裝
dry ice
儲存溫度
−20°C
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一般說明
高特异性扩增对于使用SYBR Green I染料技术成功进行qPCR至关重要,因为该染料可结合扩增过程中产生的任何dsDNA并进行检测。Taq DNA热启动聚合酶在PCR变性步骤开始之前,处于抗体介导的失活状态。
應用
- for the amplification and quantification of DNA in real-time PCR (qPCR) assay
- in the amplification and quantification of transcripts in 2-step quantitative reverse transcription polymerase chain reaction (qRT-PCR)
- in the amplification of complementary DNA (cDNA) by real-time PCR (qPCR) assay
- 基因表达
- DNA定量
- 染色质免疫沉淀(CHiP)
特點和優勢
- 只需33分钟即可获得分析结果
- 高效、灵敏的实时PCR结果
- 几乎不需要多少优化,甚至无需优化
成分
packaging:
250 reactions* = 2 X 1.25 mL tubes
1250 reactions* = 10 X 1.25 mL tubes
5000 reactions* = 1 X 50 mL tube
*number of reactions based on a 20uL volume
品質
其他說明
KiCqStart SYBR Green qPCR ReadyMix在-20°C的恒温冷冻柜中避光保存,可稳定存放1年。为方便使用,也可在+2至+8°C下储存长达6周。解冻后,充分混匀后再使用。不建议反复冻融产品。不过,冻融20次或+20°C存放2个月后,产品没有出现任何性能损失。
法律資訊
推薦
相關產品
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
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文章
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PCR assay guide navigates you through primer validation and other assay optimization factors to ensure high sensitivity and specificity for optimum DNA/ RNA quantification.
Real-time polymerase chain reaction allows researchers to estimate the quantity of starting material in a sample. It has a much wider dynamic range of analysis than conventional PCR
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條款
Quantitative PCR protocol using SYBR Green reagents. Procedure supports most qPCR instruments.
Quantitative PCR protocol using SYBR Green reagents. Procedure supports most qPCR instruments.
Analysis of gene expression data requires a stable reference or loading control. This reference is usually one or more reference genes.
Once an assay has been optimized, it is important to verify the reaction efficiency. This information is important when reporting and comparing assays. In this example protocol, the assay efficiency is compared over a wide and narrow dynamic range of cDNA concentrations.
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