Hotstart HiTaq One-Step RT-PCR Mix

Hotstart HiTaq One-Step RT-PCR Mix

有货

Hotstart HiTaq One-Step RT-PCR Mix

品牌:Jinpan
Hotstart HiTaq One-Step RT-PCR Mix

MSDS

质检证书(CoA)

相似产品

货号 (SKU) 包装规格 是否现货 价格 数量
H292648-50μl 50μL 期货 Hotstart HiTaq One-Step RT-PCR Mix  

基本信息

产品名称 Hotstart HiTaq One-Step RT-PCR Mix
英文名称 Hotstart HiTaq One-Step RT-PCR Mix
运输条件 超低温冰袋运输

一般描述

产品简介

One-Step RT-PCR Mix 以其卓越的快速性及定量性被广泛应用,使用该产品进行 Real Time  RT-PCR 反应可在同一反应管内连续进行,操作简单,并能有效防止污染。本制品中使用了最适合于 Real Time RT-PCR 的超级反转录酶(Super MMLV Reverse Transcriptase)和化学修饰热启动酶(Hotstart HiTaq DNA Polymerase),具有高扩增效率和高扩增特异性,能进行稳定的 Real Time One Step RT-PCR 反应, 大大提高了检测灵敏度,并省略了PCR 反应后的电泳步骤,非常适合于 RNA 病毒等微量 RNA 的检测。

本制品专为进行便利、高灵敏度的一步式 RT-PCR 设计。其独特的酶和特别设计的缓冲液确保了逆转录和PCR 反应高效、准确的进行,无需进行优化。可以在宽广的定量区域内得到良好的标准曲线,对靶基因进行准确定量检测,重复性好,可信度高。

产品特点

快速方便的单管反应;

适合各种 RNA 模板,无需优化反应条件;

独特的酶组合,确保反应的高特异性和高灵敏度;

经优化的缓冲体系确保了高效的逆转录和扩增过程。

产品内容

Hotstart HiTaq DNA Polymerase ( 5U/μl )

Super MMLV Reverse Transcriptase (200U/μl )

RNasin ( 40U/μl )

5×HS HiTaq One Step RT-PCR Buffer(Mg2+ Plus)

Solution I ( 10× )

dNTP Mix ( 25mM )

使用方法

1. 体系配制(50μl 体系)

组分

体积

终浓度

Hotstart HiTaq DNA Polymerase

0.75μl

Super MMLV Reverse Transcriptase

0.4μl

RNasin

0.5μl

5×HS HiTaq One Step RT-PCR Buffer

10μl

Solution I ( 10× )

5μl

dNTP Mix

0.4μl

0.2mM

Primer-probe Mix

3μl ※

模板

5μl ※

超纯水

Up to 50μl

总体积

50μl

※ 注:引物、探针以及模板的用量可自行调整,体系不够请用超纯水补齐。

2. 反应条件

步骤

温度

时间

循环数

1

50℃

15min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(收集荧光)

※注:反应条件根据引物探针和模板情况可自行设置。

Product Introduction

One-Step RT-PCR Mix is ​​widely used due to its excellent rapidity and quantification. Real Time RT-PCR reactions can be carried out continuously in the same reaction tube with this product, which is simple to operate and can effectively prevent contamination. This product uses Super MMLV Reverse Transcriptase (Super MMLV Reverse Transcriptase) and chemically modified Hotstart HiTaq DNA Polymerase, which are most suitable for Real Time RT-PCR, with high amplification efficiency and high amplification specificity. It can perform a stable Real Time One Step RT-PCR reaction, greatly improving the detection sensitivity, and omitting the electrophoresis step after the PCR reaction, which is very suitable for the detection of RNA viruses and other trace RNAs.

This product is designed for convenient and highly sensitive one-step RT-PCR. Its unique enzymes and specially designed buffers ensure that reverse transcription and PCR reactions are carried out efficiently and accurately without optimization. A good standard curve can be obtained in a wide quantitative area, and the target gene can be accurately and quantitatively detected, with good repeatability and high reliability.

Features

Quick and convenient single tube reaction;

Suitable for various RNA templates, no need to optimize reaction conditions;

Unique enzyme combination to ensure high specificity and high sensitivity of the reaction;

The optimized buffer system ensures an efficient reverse transcription and amplification process.

Product content

Hotstart HiTaq DNA Polymerase ( 5U/μl )

Super MMLV Reverse Transcriptase (200U/μl )

RNasin ( 40U/μl )

5×HS HiTaq One Step RT-PCR Buffer(Mg2+ Plus)

Solution I ( 10× )

dNTP Mix ( 25mM )

Instructions

1. System preparation (50μl system)

Reagent

Volume

Final concentration

Hotstart HiTaq DNA Polymerase

0.75μl

Super MMLV Reverse Transcriptase

0.4μl

RNasin

0.5μl

5×HS HiTaq One Step RT-PCR Buffer

10μl

Solution I ( 10× )

5μl

dNTP Mix

0.4μl

0.2mM

Primer-probe Mix

3μl ※

Template

5μl ※

Ultra-pure water

Up to 50μl

Total capacity

50μl

※ Note: The amount of primers, probes and templates can be adjusted by yourself. If the system is not enough, please use ultrapure water to make up.

2.Reaction conditions

Step

Temperature

Time

Number of cycles

1

50℃

15min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(Collect fluorescence)

※Note: The reaction conditions can be set according to the primer probe and template.

相关属性

储存温度 -20°C储存
品牌 Jinpan

Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)

Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)

有货

Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)

品牌:Jinpan
Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)

MSDS

质检证书(CoA)

相似产品

货号 (SKU) 包装规格 是否现货 价格 数量
H292677-50μl 50μL 期货 Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)  

基本信息

产品名称 Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)
英文名称 Hotstart HiTaq One-Step RT-PCR Mix(Heat-labile UDG)
运输条件 超低温冰袋运输

一般描述

产品简介

One-Step  RT-PCR  Mix(Heat-labile  UDG)以其卓越的快速性及定量性被广泛应用,使用该产品进行 Real Time RT-PCR 反应可在同一反应管内连续进行,操作简单,并能有效防止污染。本制品中使用了最适合于 Real Time RT-PCR 的超级反转录酶(Super MMLV Reverse Transcriptase)和化学修饰热启动酶(Hotstart HiTaq DNA Polymerase),具有高扩增效率和高扩增特异性。本试剂盒中引入了 dUTP/UDG 防污染系统,Heat-labile UDG 在室温下即可将含U 的污染物迅速降解,55℃逆转录时,Heat-labile UDG迅速失活,因此不会影响 RT-PCR 的效率和灵敏度。

dUTP/UDG 防污染系统是一种非常有效的控制 PCR 扩增产物污染的手段。含有比例优化的dUTP/dNTP  Mix,并加入了来源于嗜冷海洋细菌的  Heat-labile  Uracil-DNA  Glycosylase。Heat-labile Uracil-DNA Glycosylase 在室温下具有很高的活性,在反应体系混合过程中即可充分降解含U 的双链DNA污染物。当反应体系升温至 55℃  时,Heat-labile Uracil-DNA Glycosylase 迅速彻底失活,维持 cDNA 的完整性,保证检测灵敏度不受影响。

产品特点

快速方便的单管反应;

适合各种RNA 模板,无需优化反应条件;

独特的酶组合,确保反应的高特异性和高灵敏度;

经优化的缓冲体系确保了高效的逆转录和扩增过程。

产品内容

Hotstart HiTaq DNA Polymerase ( 5U/μl )

Super MMLV Reverse Transcriptase ( 200 U /μl )

RNasin ( 40U/μl )

5×HS HiTaq One Step RT-PCR Buffer(Mg2+ Plus)

Solution I ( 10× )

dN(U)TP Mix ( 20mM,A:C:G:T:U=1:1:1:1:1 )

Heat-labile Uracil-DNA Glycosylase(1U/μl)


使用方法

1. 体系配制(50μl 体系)

组分

体积

终浓度

Hotstart HiTaq DNA Polymerase

0.375μl

Super MMLV Reverse Transcriptase

0.2μl

RNasin

0.25μl

5×HS HiTaq One Step RT-PCR

5μl

Solution I ( 10× )

2.5μl

dN(U)TP Mix ( 20mM )

0.25μl

0.2mM

Heat-labile Uracil-DNA Glycosylase

0.25μl

Primer-probe Mix

1.5μl ※

模板

2.5μl ※

超纯水

Up to 25μl

总体积

25μl

※ 注:引物、探针以及模板的用量可自行调整,体系不够请用超纯水补齐。

2.反应条件

体系配制完成后,室温放置 15min 后,上机进行检测:

步骤

温度

时间

循环数

1

50℃

15min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(收集荧光)

※注:反应条件根据引物探针和模板情况可自行设置。

Product Introduction

One-Step RT-PCR Mix (Heat-labile UDG) is widely used due to its excellent rapidity and quantification. Real Time RT-PCR reactions can be carried out continuously in the same reaction tube with this product, which is simple and effective. Prevent pollution. This product uses Super MMLV Reverse Transcriptase (Super MMLV Reverse Transcriptase) and chemically modified Hotstart HiTaq DNA Polymerase, which are most suitable for Real Time RT-PCR, with high amplification efficiency and high amplification specificity. The dUTP/UDG anti-pollution system is introduced in this kit. Heat-labile UDG can rapidly degrade U-containing contaminants at room temperature. When reverse transcription at 55°C, Heat-labile UDG is rapidly inactivated, so it will not affect RT -The efficiency and sensitivity of PCR.

The dUTP/UDG anti-pollution system is a very effective means to control the contamination of PCR products. Contains optimized dUTP/dNTP Mix and added Heat-labile Uracil-DNA Glycosylase derived from psychrophilic marine bacteria. Heat-labile Uracil-DNA Glycosylase has high activity at room temperature, and it can fully degrade U-containing double-stranded DNA contaminants during the mixing process of the reaction system. When the reaction system is heated to 55°C, Heat-labile Uracil-DNA Glycosylase is quickly and completely inactivated, maintaining the integrity of the cDNA and ensuring that the detection sensitivity is not affected.

Features

Quick and convenient single tube reaction;

Suitable for various RNA templates, no need to optimize reaction conditions;

Unique enzyme combination to ensure high specificity and high sensitivity of the reaction;

The optimized buffer system ensures an efficient reverse transcription and amplification process.

Product content

Hotstart HiTaq DNA Polymerase ( 5U/μl )

Super MMLV Reverse Transcriptase ( 200 U /μl )

RNasin ( 40U/μl )

5×HS HiTaq One Step RT-PCR Buffer(Mg2+ Plus)

Solution I ( 10× )

dN(U)TP Mix ( 20mM,A:C:G:T:U=1:1:1:1:1 )

Heat-labile Uracil-DNA Glycosylase(1U/μl)

Instructions

1. System preparation (50μl system)

Reagent

Volume

Final concentration

Hotstart HiTaq DNA Polymerase

0.375μl

Super MMLV Reverse Transcriptase

0.2μl

RNasin

0.25μl

5×HS HiTaq One Step RT-PCR

5μl

Solution I ( 10× )

2.5μl

dN(U)TP Mix ( 20mM )

0.25μl

0.2mM

Heat-labile Uracil-DNA Glycosylase

0.25μl

Primer-probe Mix

1.5μl ※

Template

2.5μl ※

Ultra-pure water

Up to 25μl

Total capacity

25μl

※ Note: The amount of primers, probes and templates can be adjusted by yourself. If the system is not enough, please use ultrapure water to make up.

2. Reaction conditions

After the preparation of the system is completed, leave it at room temperature for 15 minutes, and then test it on the machine:

Step

Temperature

Time

Number of cycles

1

50℃

15min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(Collect fluorescence)

※Note: The reaction conditions can be set according to the primer probe and template.

相关属性

储存温度 -20°C储存
品牌 Jinpan

Hotstart HiTaq PCR Mix(2×)

Hotstart HiTaq PCR Mix(2×)

本试剂提供了进行简便、灵敏的 PCR 检测系统。

有货

Hotstart HiTaq PCR Mix(2×)

品牌:Jinpan
Hotstart HiTaq PCR Mix(2×)

MSDS

质检证书(CoA)

相似产品

货号 (SKU) 包装规格 是否现货 价格 数量
H292367-25μl 25μl 期货 Hotstart HiTaq PCR Mix(2×)  

基本信息

产品名称 Hotstart HiTaq PCR Mix(2×)
英文名称 Hotstart HiTaq PCR Mix(2×)
运输条件 超低温冰袋运输

一般描述

产品说明

本试剂提供了进行简便、灵敏的 PCR 检测系统。核心试剂包含了经过优化的缓冲液、dNTPs Mix、化学修饰热启动酶(Hotstart HiTaq DNA polymerase)和 MgCl2 溶液,使用者只需加入适量的引物和探针或荧光染料,即可进行荧光 PCR 检测。在反应中 Hotstart HiTaq DNA polymerase 的加入使得反应具有极强的特异性和高度灵敏度。

产品内容

Hotstart HiTaq PCR Mix

使用方法

1.PCR 反应体系的设置

a.溶解并混匀 PCR 反应所需的各种溶液,并放置于冰浴上或冰盒内。建议反应 PCR 液体分装使用, 避免反复冻融。

b.参考下表设置 PCR 反应,建议 PCR 反应体系的配置在冰浴或在冰盒上进行:

试剂

体积

终浓度

Hotstart HiTaq PCR Mix

25μl

Primer-probe Mix

3μl  ※

模板

10μl  ※

超纯水

Up to 50μl

总体积

50μl

※ 注:引物、探针以及模板的用量根据实验用量加入。

c.用移液器轻轻吹打混匀或轻微 Vortex 混匀,室温离心数秒,使液体积聚于管底。

d.各设置好的 PCR 反应管置于 PCR 仪上,开始 PCR 反应。

2.实验设置

步骤

温度

时间

循环数

1

95℃

10min

1

2

94℃

15s

 

40

3

55℃

40s(收集荧光)

注:Hotstart HiTaq DNA Polymer的热激时间10min到15min都可以,所以第二步的95℃、10 min(热启动酶热激)的时间可以根据实验要求进行设置,使用时时间从10min到15min设置都可以,比较灵活。另收集荧光设置为两步或者三步可以根据您的实验设置自行设定。

Product manual

This reagent provides a simple and sensitive PCR detection system. The core reagents include optimized buffers, dNTPs Mix, chemically modified Hotstart HiTaq DNA polymerase and MgCl2 solution. Users only need to add appropriate primers and probes or fluorescent dyes to perform fluorescent PCR detection. The addition of Hotstart HiTaq DNA polymerase in the reaction makes the reaction highly specific and highly sensitive.

Product content

Hotstart HiTaq PCR Mix

Instructions

1. PCR reaction system settings

a. Dissolve and mix the various solutions required for the PCR reaction, and place them on an ice bath or in an ice box. It is recommended that the reaction PCR liquid be used in aliquots to avoid repeated freezing and thawing.

b. Refer to the following table to set up the PCR reaction. It is recommended to configure the PCR reaction system in an ice bath or on an ice box:

Reagent

Volume

Final concentration

Hotstart HiTaq PCR Mix

25μl

Primer-probe Mix

3μl  ※

Template

10μl  ※

Ultra-pure water

Up to 50μl

Total capacity

50μl

※ Note: The amount of primers, probes and templates are added according to the amount of experiment.

c. Use a pipette to mix gently or gently Vortex to mix, and centrifuge for a few seconds at room temperature to allow the liquid to accumulate at the bottom of the tube.

d. Place each set of PCR reaction tubes on the PCR machine to start the PCR reaction.

2. Experimental settings

Step

Temperature

Time

Number of cycles

1

95℃

10min

1

2

94℃

15s

 

40

3

55℃

40s(Collect fluorescence)

Note: The heat shock time of Hotstart HiTaq DNA Polymer can be 10min to 15min, so the 95℃, 10min (hot start enzyme heat shock) time of the second step can be set according to the experimental requirements, and the time of use can be set from 10min to 15min It’s ok, it’s more flexible. In addition, the collection of fluorescence is set to two or three steps, which can be set according to your experimental settings.

相关属性

储存温度 -20°C储存
品牌 Jinpan

Hotstart HiTaq Master Mix(含UDG酶)

Hotstart HiTaq Master Mix(含UDG酶)

有货

Hotstart HiTaq Master Mix(含UDG酶)

品牌:Jinpan
Hotstart HiTaq Master Mix (with UDG enzyme)

MSDS

质检证书(CoA)

相似产品

货号 (SKU) 包装规格 是否现货 价格 数量
H292406-50μl 50μL 期货 Hotstart HiTaq Master Mix(含UDG酶)  

基本信息

产品名称 Hotstart HiTaq Master Mix(含UDG酶)
英文名称 Hotstart HiTaq Master Mix (with UDG enzyme)
运输条件 超低温冰袋运输

一般描述

产品说明

本试剂提供了进行简便、灵敏和防污染的 PCR 检测系统。核心试剂包含了经过优化的缓冲液、化学修饰热启动酶(Hotstart HiTaq DNA polymerase),使用者只需加入适量的引物和探针或荧光染料,即可进行荧光 PCR 检测。在 PCR 反应前加入 UDG 可降解 含有尿嘧啶的 PCR 产物,而对不含尿嘧啶的模板无任何影响,可选择性水解含有尿嘧啶的 PCR 产物。在反应中 Hotstart HiTaq DNA polymerase 的加入使得反应具有极强的特异性和高度灵敏度。

UDG 的作用原理:在 PCR 反应前 50℃、2min 反应中,UDG  酶可水解 PCR 反应液中含有尿嘧啶的 PCR  产物的尿嘧啶碱基和糖磷酸骨架的 N-糖苷键,释放游离尿嘧啶。随后进行 95℃、10min 热处理,在 UDG 酶失活的同时进一步对磷酸骨架水解,从而消除含有尿嘧啶的 PCR 产物的污染。UDG 酶可以作用于单链或双链 DNA,对 RNA 无活性。

产品内容

uHotstart HiTaq Master PCR Mix(25×)

u5×Hotstart HiTaq Buffer( Mg2+  Plus )

使用方法

1. 使用前请注意混匀,然后按下列组份配制 50μl 反应体系的PCR 反应液

试剂

体积

终浓度

Hotstart HiTaq Master PCR Mix(25×)

2μl

5×Hotstart HiTaq Buffer( Mg2+  Plus )

10μl

Primer-probe Mix

3μl ※

模板

20μl ※

超纯水

Up to 50μl

 

总体积

50μl

※ 注:引物、探针以及模板的用量可自行调整,体系不够请用超纯水补齐。

2. 实验设置

步骤

温度

时间

循环数

1

50℃

2min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(收集荧光)

※注:Hotstart  HiTaq  DNA  polymerase 的热激时间 10min,所以第二步的 95℃、10min(UDG 失活,热启动酶热激)的时间需要设置为 10min。另收集荧光设置为两步或者三步可以根据您的实验设置自行设定。

Product manual

This reagent provides a simple, sensitive and anti-contamination PCR detection system. The core reagents include optimized buffers and chemically modified Hotstart HiTaq DNA polymerase. Users only need to add appropriate primers and probes or fluorescent dyes to perform fluorescent PCR detection. Adding UDG before the PCR reaction can degrade PCR products containing uracil without any effect on templates without uracil, and can selectively hydrolyze PCR products containing uracil. The addition of Hotstart HiTaq DNA polymerase in the reaction makes the reaction highly specific and highly sensitive.

The working principle of UDG: In the reaction at 50°C and 2min before the PCR reaction, the UDG enzyme can hydrolyze the uracil base of the PCR product containing uracil in the PCR reaction solution and the N-glycosidic bond of the sugar phosphate backbone to release free uracil. Then heat treatment at 95°C for 10 minutes to further hydrolyze the phosphate backbone while the UDG enzyme is inactivated, thereby eliminating the contamination of PCR products containing uracil. UDG enzymes can act on single-stranded or double-stranded DNA and have no activity on RNA.

Product content

uHotstart HiTaq Master PCR Mix(25×)

u5×Hotstart HiTaq Buffer( Mg2+  Plus )

Instructions

1. Please pay attention to mixing before use, and then prepare the PCR reaction solution of 50μl reaction system according to the following components

Reagent

Volume

Final concentration

Hotstart HiTaq Master PCR Mix(25×)

2μl

5×Hotstart HiTaq Buffer( Mg2+  Plus )

10μl

Primer-probe Mix

3μl ※

Template

20μl ※

Ultra-pure water

Up to 50μl

 

Total capacity

50μl

※ Note: The amount of primers, probes and templates can be adjusted by yourself. If the system is not enough, please use ultrapure water to make up.

2. Experimental settings

Step

Temperature

Time

Number of cycles

1

50℃

2min

1

2

95℃

10min

1

3

94℃

15s

 

40※

4

55℃

40s(Collect fluorescence)

※Note: The heat shock time of Hotstart HiTaq DNA polymerase is 10min, so the time of 95℃, 10min (UDG inactivation, hot start enzyme heat shock) in the second step needs to be set to 10min. In addition, the collection of fluorescence is set to two or three steps, which can be set according to your experimental settings.

相关属性

储存温度 -20°C储存
品牌 Jinpan