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- 详细信息
- 文献和实验
- 技术资料
- 适应物种:
Human,Mouse,Rat,Chicken,Pig,Cow,Rabbit,Sheep,
- 应用范围:
WB,ICC,
- 抗体英文名:
Phospho-PPAR Gamma (ser273)
- 规格:
100ul
| 英文名称 | Phospho-PPAR Gamma (ser273) |
| 中文名称 | 磷酸化过氧化酶活化增生受体γ抗体 PPARγ |
| 别 名 | Phospho-PPAR Gamma(ser273); P-PPAR Gamma (Phospho-ser273); CIMT1; HUMPPARG; NR1C3; Nuclear receptor subfamily 1 group C member 3; PAX8/PPARG Fusion Gene; Peroxisome Proliferator Activated Receptor gamma; PPAR gamma; PPARG; PPARG1; PPARG2; PPARG3; PPARG_HUMAN. |
| 产品类型 | 磷酸化抗体 |
| 研究领域 | 肿瘤 细胞生物 信号转导 细胞凋亡 激酶和磷酸酶 表观遗传学 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, (predicted: Rat, Chicken, Pig, Cow, Rabbit, Sheep, ) |
| 产品应用 | WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 57kDa |
| 细胞定位 | 细胞核 细胞浆 |
| 性 状 | Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthesised phosphopeptide derived from human PPAR Gamma around the phosphorylation site of ser273:DK(p-S)PF |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. |
| PubMed | PubMed |
| 产品介绍 | This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. Function: Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the receptor binds to a promoter element in the gene for acyl-CoA oxidase and activates its transcription. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. Subunit: Forms a heterodimer with the retinoic acid receptor RXRA called adipocyte-specific transcription factor ARF6. Interacts with NCOA6 coactivator, leading to a strong increase in transcription of target genes. Interacts with coactivator PPARBP, leading to a mild increase in transcription of target genes. Interacts with FAM120B. Interacts with PRDM16 (By similarity). Interacts with NOCA7 in a ligand-inducible manner. Interacts with NCOA1 LXXLL motifs. Interacts with DNTTIP2, MAP2K1/MEK1, PRMT2 and TGFB1I1. Interacts with PDPK1. Interacts with ASXL1 AND ASXL2. Subcellular Location: Nucleus. Cytoplasm. Tissue Specificity: Highest expression in adipose tissue. Lower in skeletal muscle, spleen, heart and liver. Also detectable in placenta, lung and ovary. DISEASE: Note=Defects in PPARG can lead to type 2 insulin-resistant diabetes and hyptertension. PPARG mutations may be associated with colon cancer. Defects in PPARG may be associated with susceptibility to obesity (OBESITY) [MIM:601665]. It is a condition characterized by an increase of body weight beyond the limitation of skeletal and physical requirements, as the result of excessive accumulation of body fat. Defects in PPARG are the cause of familial partial lipodystrophy type 3 (FPLD3) [MIM:604367]. Familial partial lipodystrophies (FPLD) are a heterogeneous group of genetic disorders characterized by marked loss of subcutaneous (sc) fat from the extremities. Affected individuals show an increased preponderance of insulin resistance, diabetes mellitus and dyslipidemia. Genetic variations in PPARG can be associated with susceptibility to glioma type 1 (GLM1) [MIM:137800]. Gliomas are central nervous system neoplasms derived from glial cells and comprise astrocytomas, glioblastoma multiforme, oligodendrogliomas, and ependymomas. Note=Polymorphic PPARG alleles have been found to be significantly over-represented among a cohort of American patients with sporadic glioblastoma multiforme suggesting a possible contribution to disease susceptibility. Similarity: Belongs to the nuclear hormone receptor family. NR1 subfamily. Contains 1 nuclear receptor DNA-binding domain. SWISS: P37231 Gene ID: 5468 Database links: Entrez Gene: 5468 Human Entrez Gene: 19016 Mouse SwissProt: P37231 Human SwissProt: P37238 Mouse Unigene: 162646 Human Unigene: 3020 Mouse Unigene: 23443 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
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文献和实验【求助】PPARγ基因的序列参与者:清风一号有谁能提供PPARγ基因的序列吗?我将十分感激,谢谢!!!!参与者:yangea楼主的描述不清楚,PPARγ基因的序列,哪个种属?楼主可以按照下述方法自己查找所需要的:1、打开ncbi的主页2、在search项下拉菜单中选择gene,同时在右边for查找项后输入您需要查找的项目,如PPARγ AND Homo sapiens或PPARγ AND Mus musculus(并列上种属,缩小查找范围)3、找所列出信息与所查最为相关的项,点击进入4、会看到
重磅!Science 子刊揭示 T 细胞受体的「秘密生活」及其在免疫反应中的作用
T 细胞抗原受体 (T cell receptor, TCR) 是一种多亚基复合体,通过结合抗原提呈细胞 (APC) 表面的抗原肽 - MHC 分子复合物(pMHC)来特异性识别抗原,对 T 细胞发挥免疫功能至关重要。TCR 可以识别「自我」和「非我」抗原,并根据抗原的特质引发特异性的下游信号通路,从而使得 T 细胞产生特异性分化并获得不同的效应功能。TCR 有 4 种 CD3 信号链(CD3γ/δ/ε/ζ),共携带了 20 个酪氨酸磷酸化位点。不同的抗原刺激会引起不同的 TCR 磷酸化模式
121 不论是经典型还是新型PKC,我师姐都是用转位来判断其活化的。她分别提膜蛋白和胞浆蛋白,都用的actin做内参 蛋蛋豆豆 cgaoy121 这里面还涉及转位吗?我想请教各位究竟怎么测PKC啊,在无法确定分型的情况下 cgaoy121 磷酸化和转位是判断PKC活化的两种方法,不是吗。用WB测PKC,转位的话就提胞浆胞膜蛋白,用某一亚型的PKC抗体检测,磷酸化的方法就提总蛋白,用磷酸化抗体测磷酸化
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