CST logo

#5098 SimpleChIP® Human AFM Intron 1 Primers

 
CSTコード 包装
希望納入価格 (円)
国内在庫 i
2019年12月6日15時40分 現在
ご登録代理店情報 i
カスタマー情報にご登録いただいた代理店を表示しています。
ご登録代理店の変更はこちら
#5098S500 μL42,000
ログインすると国内在庫状況がご確認いただけます。
Directions For Use
  1. Label the appropriate number of PCR tubes or PCR plates compatible with the model of real-time PCR machine to be used. PCR reactions should be performed in duplicate and should include a tube with no DNA to control for contamination, and a serial dilution of a 2% total input chromatin DNA (undiluted, 1:5, 1:25, 1:125), which is used to create a standard curve and determine amplification efficiency.
  2. Add 2 µl of the appropriate ChIP DNA sample to each tube or well of the PCR plate.
  3. Prepare a master PCR reaction mix as described below. Add enough reagents for two extra reactions to account for loss of volume. Add 18 µl of the master PCR reaction mix to each PCR reaction tube or well of the PCR plate.

Reagent Volume for 1 PCR Reaction (20 µl)

Nuclease-free H2O 6 µl
5 µM SimpleChIP® Primers 2 µl
2X SYBR® Green Reaction Mix 10 µl
  1. Start the following PCR reaction program:
    1. Initial Denaturation: 95°C for 3 min.
    2. Denaturation: 95°C for 15 sec.
    3. Anneal and Extension: Primer-specific temp. for 60 sec.
    4. Repeat steps b and c for a total of 40 cycles.
  2. Analyze quantitative PCR results using software provided with the real-time PCR machine.
5098 の推奨プロトコール i

最適な結果を得るために:Cell Signaling Technology (CST) 社は、各製品の推奨プロトコールを使用することを強くお薦めいたします。
推奨プロトコールはCST社内試験の徹底的なバリデーションに基づいて作成されておりますので、正確かつ再現性の高い結果が得られます。

注:各製品に最適化されたプロトコールをリンクしています。

 
貯法
-20℃
社内データ

PCR Efficiency

PCR Efficiency

SimpleChIP® Human AFM Intron 1 Primers were tested on DNA isolated from cross-linked cells using the SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. Real-time PCR was performed in duplicate on a serial dilution of 2% total input DNA (20 ng, 4 ng, 0.8 ng, and 0.16 ng) using a real-time PCR detection system and SYBR® Green reaction mix. The PCR amplification efficiency (E) and correlation coefficient (R2) were calculated based on the corresponding threshold cycle (CT) of each dilution sample during 40 cycles of real-time PCR (95°C denaturation for 15 sec, 60°C anneal/extension for 60 sec).

Melt Curve

Melt Curve

PCR product melting curves were obtained for real-time PCR reactions performed using SimpleChIP® Human AFM Intron 1 Primers. Data is shown for both duplicate PCR reactions using 20 ng of total DNA. The melt curve consists of 80 melt cycles, starting at 55°C with increments of 0.5°C per cycle. Each peak is formed from the degradation of a single PCR product.

バックグラウンド

The chromatin immunoprecipitation (ChIP) assay is a powerful and versatile technique used for probing protein-DNA interactions within the natural chromatin context of the cell (1,2). This assay can be used to either identify multiple proteins associated with a specific region of the genome or to identify the many regions of the genome bound by a particular protein (3-6). ChIP can be used to determine the specific order of recruitment of various proteins to a gene promoter or to "measure" the relative amount of a particular histone modification across an entire gene locus (3,4). In addition to histone proteins, the ChIP assay can be used to analyze binding of transcription factors and co-factors, DNA replication factors, and DNA repair proteins. When performing the ChIP assay, cells are first fixed with formaldehyde, a reversible protein-DNA cross-linking agent that "preserves" the protein-DNA interactions occurring in the cell (1,2). Cells are lysed and chromatin is harvested and fragmented using either sonication or enzymatic digestion. Fragmented chromatin is then immunoprecipitated with antibodies specific to a particular protein or histone modification. Any DNA sequences that are associated with the protein or histone modification of interest will co-precipitate as part of the cross-linked chromatin complex and the relative amount of that DNA sequence will be enriched by the immunoselection process. After immunoprecipitation, the protein-DNA cross-links are reversed and the DNA is purified. Standard PCR or quantitative real-time PCR are often used to measure the amount of enrichment of a particular DNA sequence by a protein-specific immunoprecipitation (1,2). Alternatively, the ChIP assay can be combined with genomic tiling micro-array (ChIP on chip) techniques, high throughput sequencing (ChIP-Seq), or cloning strategies, all of which allow for genome-wide analysis of protein-DNA interactions and histone modifications (5-8). SimpleChIP® primers have been optimized for amplification of ChIP-isolated DNA using real-time quantitative PCR and provide important positive and negative controls that can be used to confirm a successful ChIP experiment.

使用例
製品をご使用いただいて研究を発表されましたら、ぜひお知らせください
 
関連製品
4473   Pan-Methyl-Histone H3 (Lys9) (D54) XP® Rabbit mAb
4658   Di-Methyl-Histone H3 (Lys9) (D85B4) XP® Rabbit mAb
9002   SimpleChIP® Enzymatic Chromatin IP Kit (Agarose Beads)
9003   SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads)
9006   ChIP-Grade Protein G Magnetic Beads
9007   ChIP-Grade Protein G Agarose Beads
9728   Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb
9753   Di-Methyl-Histone H3 (Lys9) Antibody

SYBR is a registered trademark of Molecular Probes, Inc.
SimpleChIP is a registered trademark of Cell Signaling Technology, Inc.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

本製品は試験研究用です。

SimpleChIP® Human AFM Intron 1 Primers

Metabolic Reprogramming in Disease

お薦めリンク

テクニカルサポート

製品特集

Applications