·产品描述

   DNA羟甲基化修饰是基因组表观遗传学的重要调控方式，指5-甲基胞嘧啶(5-mC)在TET蛋白家族的催化作用下氧化生成5-羟甲基胞嘧啶(5-hmC)，完成DNA胞嘧啶的去甲基化过程。基因组甲基化异常导致了多种肿瘤的发生，DNA甲基化和羟甲基化是两种独立的表观改变，有研究表明两者有相反的功能作用，羟甲基化修饰作为去甲基化的一种，同样与肿瘤发生密不可分。

   MethylFlash Global DNA Hydroxymethylation (5-hmC) ELISA Easy Kit（P-1032）是经过全新优化的、完整的的试剂组合，可以利用抗体结合和ELISA原理方式，定量分析DNA中5-hmc。它可以直接检测哺乳动物，植物，真菌细菌，病毒，细胞，组织，血清/血浆以及其它体液中的总DNA样本的5-hmc的甲基化程度。

·产品特点

1· 快速实验：优化实验操作，完成实验仅需2h 

2· 灵敏度：最低可检测0.01%的羟甲基化水平DNA 

3· 特异性：不与未修饰的胞嘧啶或者其它修饰的胞嘧啶有任何交叉反应 

4· 精确性：最优化的阳性对照标准品，提供堪比HPLC-MS的可靠结果 

5· 一致性：简化的操作流程，有效降低复孔间的变异系数（CV%） 

6· 完整性：试剂盒提供阳性对照与阴性对照，而无需额外试剂

·产品说明书

The MethylFlash™ Global DNA Hydroxymethylation (5-hmC) ELISA Easy Kit (Colorimetric) is a complete set of optimized buffers and reagents to colorimetrically quantify global DNA hydroxymethylation status by specifically measuring levels of 5-hydroxymethylcytosine (5-hmC) in a simplified, “one-step” ELISA-like format. As a fourth generation technology of Epigentek's popular global DNA methylation technique, it is a further refinement of the predecessor MethylFlash kit by improving upon speed, simplicity, sensitivity, and reproducibility.

This kit is also specifically optimized for paired use with the MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (Colorimetric) for simultaneously quantifying both methylated DNA and hydroxymethylated DNA.

This kit has the following advantages and features:

• Fast - Reduced steps so that the entire procedure only needs 2 hours*
• Robust - Improved kit composition allows the assay to have a greater “signal window” with reduced variation between replicates
• Convenient - Inherently low background noise, thereby eliminating the need for DNA denaturation and plate blocking steps
• Sensitive - Detection limit can be as low as 0.01% hydroxymethylated DNA from 100 ng of input DNA
• Specific - High specificity to 5-hmC, with no cross-reactivity to unmethylated cytosine or methylated cytosine within the indicated concentration range of the sample DNA
• Universal – Positive and negative controls and allow detection of DNA hydroxymethylation in any species from either single-stranded or double-stranded input DNA
• Accurate - Optimized positive controls that can be fractionalized in percentage scale, allowing the assay to be more accurate and highly comparable with HPLC-MS analysis
• Flexible - Strip-well microplate format makes the assay available for manual or high throughput analysis

* Based on a single sample assay in duplicate

Background
5-hydroxymethylcytosine (5-hmC), as a sixth DNA base with functions in transcription regulation, has been detected to be abundant in human and mouse brains and embryonic stem (ES) cells. In mammals, it can be generated by the oxidation of 5-mC, a reaction mediated by the ten-eleven translocation (TET) family of 5-mC-hydroxylases. 5-hmC has been demonstrated to be tissue specific, ranging from undetectable levels in cultured cell lines to 0.6% in human brain tissues, and can be as high as 8% of total DNA in some other species. The biological significance of 5-hmC as an important epigenetic modification in phenotype and gene expression has been recently recognized. For example, global decrease in 5-hmC content (DNA hypomethylation) has been exhibited in nearly all cancers and has been proposed as a molecular marker and therapeutic target in cancer as well. 

Principle & Procedure
This kit contains all reagents necessary for the quantification of global DNA hydroxymethylation. In this assay, DNA is bound to strip-wells that are specifically treated to have a high DNA affinity. The hydroxymethylated fraction of DNA is detected using a 5-hmC mAb-based detection complex in a one-step manner and then quantified colorimetrically by reading the absorbance in a microplate spectrophotometer. The percentage of hydroxymethylated DNA is proportional to the OD intensity measured.

Starting Materials
Input DNA should be relatively pure with 260/280 ratio >1.6 and can be diluted with water or TE buffer. The DNA amount can range from 20 ng to 200 ng per reaction. However, we recommend using 100 ng of DNA, which is the optimized input amount for the best results. 

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