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英文名称:EpiQuik Chromatin Immunoprecipitation(ChIP) Kit

中文名称:染色质免疫共沉淀(ChIP)试剂盒

供应商:Epigentek

产品货号:P-2002-1/P-2002-2/P-2002-3

目录价:4470.4/7163.2/10577.6

规格:24Reactions/48Reactions/96Reactions

名称:染色质免疫共沉淀(ChIP)试剂盒
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·产品描述

       EpiQuik 染色质免疫共沉淀(ChIP)试剂盒可以进行染色质免疫共沉淀实验,速度快,操作方便,比时下同类的其它试剂盒更加优越,安全系数高.本试剂盒即时可用,提供了检测实验所需的所有试剂和方法,无须接触放射性材料,不使用特殊设备.试剂盒获得的染色质可用来进行定性和定量PCR、southern 印迹以及DNA微阵列分析.

       EpiQuik 组织染色质免疫共沉淀(ChIP)试剂盒提供了对细胞样品进行染色质免疫沉淀反应所需的所有试剂.并且本试剂盒中含有一种阳性对照抗体(RNA聚合酶II抗体)、一种阴性对照抗体(正常小鼠的IgG)、GAPDH引物(可以作为阳性对照来保证试剂盒中试剂和操作步骤没出现问题).在大多数生长期的哺乳动物细胞中,RNA聚合酶II会在GAPDH基因启动子上富集,准备起始转录,因此该启动子能与RNA聚合酶II发生免疫沉淀反应,而不能与正常小鼠IgG发生.在本染色质免疫沉淀反应中,细胞耦合了甲醛,提取出其中的染色质.染色质进行适当的打断,然后加入到微孔中与其表面上吸附的抗体发生免疫反应.特异性结合到微孔上的DNA从抗体-捕获蛋白-DNA复合物上释放出来,翻转后,通过本公司专门设计的高速离心柱纯化.洗脱下来的DNA可用于随后的各种分析.该染色质免疫共沉淀(ChIP)试剂盒内主要产品组份包括:CP1 (Wash Buffer) CP2 (Antibody Buffer) CP3A (Lysis Buffer) CP3B (Lysis Buffer) CP4 (ChIP Dilution Buffer) CP5 (DNA Release Buffer) CP6 (Reverse Buffer) CP7 (Binding Buffer) CP8 (Elution Buffer) Protease Inhibitor Cocktail (100X) Normal Mouse IgG (1 mg/ml) Anti-RNA Polymerase II (1mg/ml) Proteinase K (10 mg/ml) Control Primer (GAPDH) Forward (20 uM) Reverse (20 uM) 8-Well Assay Strips (with Frame) 8-Well Strip Caps F-Spin Column F-Collection Tube 用户指南手册。


·产品特点

1、市场上同类产品中最快捷的试剂盒,整个处理过程不到5小时,得到让您满意的结果;对CHIP过程进行了彻底的简化,操作简捷,方便易学; 

2、96孔板模式使研究人员能根据自己需要选择手工或是高通量分析; 

3、附有DNA纯化柱子:大量减少不必要的重复劳动; 

4、操作简便、结果可靠、统一的分析条件;


·产品说明书


Input Type:Chromatin
Research Area:Chromatin & Transcription
Target Application:Immunoprecipitation
Vessel Format:96-Well Plate
100% Guarantee:6 months


Product Overview

The EpiQuik™ Chromatin Immunoprecipitation (ChIP) Kit is a complete set of optimized reagents to perform chromatin immunoprecipitation (ChIP) via a convenient, microplate-based format. The kit is ready-to-use and provides all the essential components needed to carry out a successful ChIP experiment. The EpiQuik™ ChIP kits are suitable for combining the specificity of immunoprecipitation with qualitative and quantitative PCR, ChIP-Seq, and ChIP-on-chip. This kit has the following advantages:

  • Fast and easy microplate-based procedure, that can be completed within 5 hours.
  • Strip microwell format makes the assay flexible: manual or high throughput.
  • Columns for DNA purification are included: save tremendous amounts of time and reduce unnecessary physical labor.
  • Compatible with all DNA amplification-based approaches.
  • Achieves very reliable and consistent assay conditions.

See also a quick chart to compare ChIP kits.

Background Information
Protein-DNA interaction plays a critical role in cellular functions such as signal transduction, gene transcription, chromosome segregation, DNA replication and recombination, and epigenetic silencing. Identifying the genetic targets of DNA binding proteins and knowing the mechanisms of protein-DNA interaction is important for understanding the cellular process. Chromatin Immunoprecipitation (ChIP) offers an advantageous tool for studying protein-DNA interactions. Unlike other methods such as EMASA, DNA microarrays, and report gene assays which analyze direct interactions between protein and DNA in vitro- ChIP can detect that a specific protein binds to the specific sequences of a gene in living cells. 

Principle & Procedure
This ChIP kit includes a positive control antibody (RNA polymerase II), a negative control normal mouse IgG, and GAPDH primers that can be used as a positive control to demonstrate the efficacy of the kit reagents and protocol. RNA polymerase II is considered to be enriched in the GAPDH gene promoter that is expected to be undergoing transcription in most growing mammalian cells and can be immunoprecipitated by RNA polymerase II but not by normal mouse IgG. In this ChIP, cells are cross-linked with formaldehyde and chromatin is extracted. The chromatin is then sheared and added into the microwell immobilized with affinity antibodies. Cross-linked DNA is released from antibody-captured protein-DNA complex, reversed and purified through the specifically designed F-Spin Column. Eluted DNA can be used for various downstream applications.

Starting Materials
Starting materials can include various cell samples. In general, the input amount should be from 500,000 to 2,000,000 cells for each reaction.


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