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- 详细信息
- 文献和实验
- 技术资料
- 抗体英文名:
HDAC2 Antibody (IP Preferred)
- 抗原:
synthetic peptide corresponding to the carboxy terminus of the human HDAC2 protein
- 应用范围:
W, IP
- 宿主:
Rabbit
- 保质期:
详见说明书
- 级别:
详见MSDS文件
- 适应物种:
H,M,Mk
- 供应商:
CST
- 库存:
大量
- 是否单克隆:
2
- 保存条件:
-20°c
- 规格:
100 ul (10 western blots)/carrier free & custom formulation / quantity
| 规格: | 产品价格: | ¥请询价 | |
|---|---|---|---|
| 规格: | 100 ul (10 western blots) | 产品价格: | ¥请询价 |
| 规格: | carrier free & custom formulation / quantity | 产品价格: | ¥请询价 |
pathway more info application references datasheet PDF MSDS PDF protocols
Applications Key: W=Western Blotting IP=Immunoprecipitation
Reactivity Key: H=Human M=Mouse Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
| Applications | Reactivity | Sensitivity | MW (kDa) | Source |
|---|---|---|---|---|
| W IP | H M Mk | Endogenous | 60 | Rabbit |
| Protocols |
|
|---|---|
| Specificity / Sensitivity | HDAC2 Antibody (IP Preferred) detects endogenous levels of total HDAC2 protein and is the preferred antibody for immunoprecipitation. The antibody does not cross-react with other HDAC proteins. |
| Source / Purification | Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the carboxy terminus of the human HDAC2 protein. Antibodies are purified by peptide affinity chromatography. Western Blotting
Western blot analysis of extracts from 293 and DLD-1 cells using HDAC2 Antibody (IP Preferred). IP
Immunoprecipitation/Western blot analysis of extracts from 293 cells. Lane 1 contains lysate input (5%), lane 2 was immunoprecipitated with HDAC2 Antibody (IP Preferred) and lane 3 was immunoprecipitated with non-specific rabbit IgG. Western blot analysis was performed using HDAC2 Antibody (IP Preferred). |
| Background | Acetylation of the histone tail causes chromatin to adopt an "open" conformation, allowing increased accessibility of transcription factors to DNA. The identification of histone acetyltransferases (HATs) and their large multiprotein complexes has yielded important insights into how these enzymes regulate transcription (1,2). HAT complexes interact with sequence-specific activator proteins to target specific genes. In addition to histones, HATs can acetylate nonhistone proteins, suggesting multiple roles for these enzymes (3). In contrast, histone deacetylation promotes a "closed" chromatin conformation and typically leads to repression of gene activity (4). Mammalian histone deacetylases can be divided into three classes on the basis of their similarity to various yeast deacetylases (5). Class I proteins (HDACs 1, 2, 3, and 8) are related to the yeast Rpd3-like proteins, those in class II (HDACs 4, 5, 6, 7, 9, and 10) are related to yeast Hda1-like proteins, and class III proteins are related to the yeast protein Sir2. Inhibitors of HDAC activity are now being explored as potential therapeutic cancer agents (6,7). HDAC1 and HDAC2 are highly homologous and are involved in histone deacetylation, chromatin remodeling and transcriptional repression (8-10). Both proteins are found together in numerous complexes including the nucleosome remodeling and deacetylation complex (NuRD), MeCP1, and the mSin3A corepressor complex.
|
| Application References | Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know ! |
| Companion Products |
For Research Use Only. Not For Use In Diagnostic Procedures. |
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文献和实验) 2、Input 条带清晰,co-IP 条带很弱? 设X为诱饵蛋白,Y 为靶蛋白,有可能为 X 和 Y 的相互作用本身比较弱 X 蛋白并不是 Y 的唯一,只部分 Y 与 X 互作 可以尝试反向拉,比如用 Y 去拉 X,可能效果比较好 3、我的 p 53 蛋白正好和抗体重链分子量接近,要如何减少抗体干扰? 建议方案: IP/WB 一抗使用不同种属来源,选择与IP抗体种属无交叉反应的二抗(Cross Adsorbed secondary antibody) 特殊二抗:比如仅识别重链或者轻链的二抗,或者仅
IP Issues in the Therapeutic Antibody Industry
The following section is related to IP issues in the therapeutic Antibody industry. A rough overview over protected enabling techniques and compounds is provided, in order to facilitate the entry into freedom to operate studies. Furthermore
Protocol for Co-IP of different proteins with RFP-MeCP2 Preperation of cells (for p100): • 1st day split 293T EBNA cells in DMEM (high glucose + 10% FCS + 5mM glutamine + 5µg/ml gentamycine) • 2nd day cells
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