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Rabbit抗原名称
HDAC3分子别名
Histone deacetylase 3; HD3; Protein deacetylase HDAC3; Protein deacylase HDAC3; RPD3-2; SMAP45免疫原
Synthetic Peptide细胞定位
Cytoplasm, NucleusAccession
O15379抗体类型
Polyclonal antibody抗体同种型
IgG应用
ICFCM ,ICC ? ,WB稀释度
应用 稀释度 推荐种属 WB 1:1000 Hu, Ms, Rt ICC 1:500 Hu, Ms ICFCM 1:50 Hu, Ms 反应种属 ?
Hu, Ms, Rt阳性样本
HeLa, K562, Jurkat, HepG2, MCF7, NIH/3T3, mouse brain, PC-12, C6, rat brain预测反应种属
(反应种属缩写表)Hm, Vt纯化方式
Immunogen Affinity浓度
0.5 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
储存条件
12 months from date of receipt / reconstitution, -20 °C as supplied
Histone deacetylase 3 (HDAC3) is a class I HDAC that plays a critical role in chromatin remodeling and gene transcription regulation. It is unique among HDACs due to its ability to shuttle between the nucleus and cytoplasm, allowing it to exert both enzymatic and non-enzymatic functions. HDAC3 primarily functions as a co-repressor, interacting with nuclear receptor co-repressors (NCoR) or silencing mediator of retinoic and thyroid receptors (SMRT) to deacetylate histones and repress gene expression. This activity is crucial for various physiological processes, including embryonic development, circadian rhythms, and metabolism. Additionally, HDAC3 is implicated in several diseases, such as cancer, neurodegeneration, and cardiovascular diseases, making it a target for therapeutic interventions. Its role in inflammation is also significant, as it regulates pro-inflammatory gene expression in macrophages. HDAC3 inhibitors are being explored for their potential in treating these conditions, with specific inhibitors showing promise in reducing side effects compared to general HDAC inhibitors.
免疫印迹
WB result of HDAC3 Rabbit pAb
Primary antibody: HDAC3 Rabbit pAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: K562 whole cell lysate 20 µg
Lane 3: Jurkat whole cell lysate 20 µg
Lane 4: HepG2 whole cell lysate 20 µg
Lane 5: MCF7 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 49 kDa
Observed MW: 48 kDaWB result of HDAC3 Rabbit pAb
Primary antibody: HDAC3 Rabbit pAb at 1/1000 dilution
Lane 1: NIH/3T3 whole cell lysate 20 µg
Lane 2: mouse brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 49 kDa
Observed MW: 48 kDaWB result of HDAC3 Rabbit pAb
Primary antibody: HDAC3 Rabbit pAb at 1/1000 dilution
Lane 1: PC-12 whole cell lysate 20 µg
Lane 2: C6 whole cell lysate 20 µg
Lane 3: rat brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 49 kDa
Observed MW: 48 kDa
流式分析
Flow cytometric analysis of K562 (Human chronic myelogenous leukemia lymphoblast) labelling HDAC3 antibody at 1/50 dilution (1 μg) / (Red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti - Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody.
Flow cytometric analysis of NIH/3T3 (Mouse embryonic fibroblast) labelling HDAC3 antibody at 1/50 dilution (1 μg) / (Red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti - Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody.
免疫细胞化学
ICC shows positive staining in NIH/3T3 cells. Anti- HDAC3 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
ICC shows positive staining in K562 cells. Anti- HDAC3 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
FAQs
我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

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