搜索历史清除全部记录

最多显示8条历史搜索记录噢~

全部

全部
产品管理
新闻资讯
介绍内容
企业网点
常见问题
企业视频
企业图册

昵称 | 退出

首页

高产T7生物素11RNA标记试剂盒(CTP)

高产T7生物素11RNA标记试剂盒(CTP)，HighYield T7 Biotin11 RNA Labeling Kit (CTP-based)，设计用于通过体外转录生产具有 11 个原子连接体的随机生物素修饰 RNA 探针。这种探针非常适合原位杂交和 Northern 印迹实验。更多视频请关注视频号【艾维缔】。哔哩哔哩【IVDSHOW】。抖音【军哥聊表观】。

关键词

所属分类

RNA修饰检测

目录号

RNT401BIOX

获取报价

猜你喜欢

产品描述
产品组分
文件资源
营销中心
注意事项
FAQ
文献追踪

For general laboratory use.

Shipping: shipped on gel packs

Storage Conditions: store at -20 °C
avoid freeze/thaw cycles

Shelf Life: 12 months

Description:
HighYield T7 Biotin11 RNA Labeling Kit (CTP-based) is designed to produce randomly Biotin-modified RNA probes with a 11-atom linker via in vitro transcription. Such probes are ideally suited for in situ hybridization and Northern Blot experiments.
Biotin-11-CTP is efficiently incorporated into RNA as substitute for its natural counterpart CTP using an optimized reaction buffer and T7 RNA Labeling Polymerase Mix.
35 % Biotin-11-CTP substitution typically results in an optimal balance between reaction and labeling efficiency. Individual optimization of Biotin-11-CTP/CTP ratio however, can easily be achieved with the single nucleotide format.
The resulting Biotin-modified RNA probe with a 11-atom linker can subsequently be detected by HRP- or AP-modified streptavidin.
The kit contains sufficient reagents for 30 labeling reactions of 20 μl each (35 % Biotin-11-CTP substitution, 1 mM ATP, GTP, UTP, 0.65 mM CTP, 0.35 mM Biotin-11-CTP).

Content:
HighYield T7 RNA Labeling Polymerase Mix
2x 40 μl, incl. RNase inhibitor and 50 % glycerol (v/v)

HighYield T7 Reaction Buffer
1x 200 μl (10x), HEPES-based

ATP - Solution
1x 100 μl (100 mM)

GTP - Solution
1x 100 μl (100 mM)

CTP - Solution
1x 100 μl (100 mM)

UTP - Solution
1x 100 μl (100 mM)

Biotin-11-CTP
1x 30 μl (10 mM)

T7 G-initiating control template (1.4 kbp)
1x 10 μl (200 ng/μl), 1.4 kbp PCR fragment plus T7 class III phi6.5 promotor resulting in approx. 1400 nt RNA transcript

PCR-grade water
1x 1.2 ml

DTT
1x 150 μl (100 mM)
To be provided by user
T7 Promotor-containing DNA template
RNA purification tools
RNAse-free DNAse I (optional)

1. Important Notes (Read before starting)
1.1 Prevention of RNAse contamination
Although a potent RNase Inhibitor is included, creating a RNAse-free work environment and maintaining RNAse-free solutions is critical for performing successful in vitro transcription reactions. We therefore recommend

to perform all reactions in sterile, RNAse-free tubes using sterile pipette tips.
to wear gloves when handling samples containing RNA.
to keep all components tightly sealed both during storage and reaction procedure.

1.2 Template requirements

Template type: Linearized plasmid DNA or PCR products containing a double-stranded T7 class II phi2.5 or class III phi6.5 promotor region upstream of the target sequence. Transcription initiation from T7 class III promotor is generally more efficient than initiation from T7 class II promotor.
Minimum T7 promotor sequences:

T7 class III phi6.5 promotor
5'-TAATACGACTCACTATAGNN…-3’
Bold: First base incorporated into RNA, NN: ideally CG

T7 class II phi2.5 promotor
5'-TAATACGACTCACTATTANN…-3'
Bold: First base incorporated into RNA, NN: ideally GG

Template quality: DNA template quality directly influences yield and quality of transcription reaction. Linearized plasmid DNA needs to be fully digested and to be free of contaminating RNase, protein and salts. We recommend selecting restriction enzymes that generate blunt ends or 5'-overhangs and purification by phenol/chloroform extraction. A PCR mixture can be used directly however, better yields will usually be obtained with purified PCR products (e.g. via silica-membrane based purification columns).

2. Preparation of working solutions
2.1 Preparation of 10 mM ATP/GTP/UTP working solution

Thaw 100 mM ATP, 100 mM GTP and 100 mM UTP solutions on ice, voretex and spin-down briefly.
Prepare a 1:10 dilution with PCR-grade water to achieve a final concentration of 10 mM (e.g. 5 μl 100 mM ATP + 5 μl 100 mM GTP + 5 μl 100 mM UTP + 35 μl PCR-grade water).
10 mM ATP/GTP/UTP working solution can be stored at -20°C. Avoid freeze/thaw cycles.

2.2 Preparation of 10 mM CTP working solution

Thaw 100 mM CTP solution on ice, voretex and spin-down briefly.
Prepare a 1:10 dilution with PCR-grade water to achieve a final concentration of 10 mM (e.g. 5 μl 100 mM CTP + 45 μl PCR-grade water).
10 mM CTP working solution can be stored at -20 °C. Avoid freeze/thaw cycles.

3. In vitro Transcription protocol
The protocol is optimized for 0.5 μg - 1 μg DNA template.
An optimal balance between reaction and labeling efficiency is typically achieved with 35% Biotin-11-CTP substitution following the standard protocol below however, individual optimization might improve results for individual applications (e.g. 2.5 mM ATP, GTP, UTP, 0.2 mM CTP, 0.1 mM Biotin-11-CTP)

Place HighYield T7 RNA Polymerase Mix on ice.
Thaw all remaining components at room temperature (RT), mix by voretexing and spin down briefly.
Assemble all components at RT to a nuclease-free microtube (sterile pipette tips) in the following order:
Mix PCR-grade water, HighYield T7 Reaction Buffer and DTT by voretexing and spin down briefly.
Add nucleotide solutions and template DNA, vortex and spin down briefly.
Add HighYield T7 RNA Labeling Polymerase Mix vortex and spin down briefly.
Incubate for 30 min at 37 °C in the dark (e.g. PCR cycler). Depending on the RNA probe individual optimization may increase product yield (2h – 4h at 37 °C).

Component	Volume	Final concenctration
PCR-grade water	X μl
HighYield T7 Reaction Buffer (10x)	2 μl	1x
100 mM DTT	2 μl
10 mM ATP/GTP/ UTP working solution (s. 2.1)	2 μl	1 mM
10 mM CTP working solution (s. 2.2)	1.3 μl	0.65 mM
10 mM Biotin-11-CTP	0.7 μl	0.35 mM
Template DNA	X μl	0.5 - 1 μg
HighYield T7 RNA Labeling Polymerase Mix	2 μl
Total volume	20 μl

Please note: Reagents for the following steps are not provided within this kit.

DNA template removal (optional)
Depending on the down-stream application, removal of template DNA might be required. We recommend a salt-resistant, high efficiency DNAase such as Turbo™DNAse (ThermoFisher). Follow the manufacturer instructions.

RNA purification
Purification of RNA is required for certain applications such as measurement of Biotin11-labelled RNA probe concentration. Spin column purification will remove proteins, salts and unincorporated nucleotides. Please follow the manufacturer instructions and ensure that the columns match with product size and possess a sufficient binding capacity (e.g. RNA Clean & Concentrator™ columns (Zymo Research) or Monarch® RNA Cleanup kit (NEB)). Other RNA purification methods such as LiCl precipitation may work but have not been tested.

RNA quantitation
RNA concentration can be determined by absorbance measurement at 260 nm (A₂₆₀) according to the Law-of-Lambert-Beer (A₂₆₀ = 1 correspond to 40 μg/ml ssRNA).

产品组分

内容	型号	规格	储存温度
高产T7生物素11RNA标记试剂盒(CTP)	RNT401BIOX-01	30次x20ul	-20°C
高产T7生物素11RNA标记试剂盒(CTP)	RNT401BIOX-02	60次x20ul	-20°C
操作手册	1	1	室温

文件资源
文件下载
文件内容
资源说明
RNT401BIOX-高产T7生物素11RNA标记试剂盒
操作手册
RNT401BIOX-高产T7生物素11RNA标记试剂盒相关单页
宣传单页
营销中心
注意事项

保存建议厂家推荐蓝冰运输。当您收到产品后，按照说明书建议保存于-20°C。
FAQ
The MTNR1A mRNA is stabilized by the cytoplasmic hnRNPL in renal tubular cells.

Yen-Sung Huang, Kuo-Cheng Lu, Tai-Kuang Chao

Journal of cellular physiology | 2020 Jul 30 | PubMed ID: 32730662

文件下载	文件内容	资源说明
	RNT401BIOX-高产T7生物素11RNA标记试剂盒	操作手册
	RNT401BIOX-高产T7生物素11RNA标记试剂盒相关单页	宣传单页

搜索历史清除全部记录

高产T7生物素11RNA标记试剂盒(CTP)

产品组分

文件资源

营销中心

注意事项

FAQ