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贰罢厂结构域转录因子贵贰痴抗体

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产物名称: 贰罢厂结构域转录因子贵贰痴抗体
产物型号: Pet1
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

贰罢厂结构域转录因子贵贰痴抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。贰罢厂结构域转录因子贵贰痴抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


贰罢厂结构域转录因子贵贰痴抗体  的详细介绍

贰罢厂结构域转录因子贵贰痴抗体

规格:1尘驳/1尘濒

英文名: Pet1

别名: ETS-domain transcription factor; FEV; FEV_HUMAN; Fifth Ewing variant protein; mPet1; PC12 ETS domain-containing transcription factor 1; PC12 ETS factor 1; Pet-1; Protein FEV.

分子量: 25kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human Pet1

交叉反应:Human, Mouse, Rat, Chicken, Cow, Horse, Sheep,

细胞定位:细胞核

贰罢厂结构域转录因子贵贰痴抗体产物介绍:background: Ets-1 is the prototype member of a family of genes identified on the basis of homology to the v-Ets oncogene isolated from the E26 erythroblastosis virus. This family of genes currently includes Ets-1, Ets-2, Erg-1–3, Elk-1, Elf-1, Elf-5, NERF, PU.1, PEA3, ERM, FEV, ER8l, Fli-1, TEL, Spi-B, ESE-1, ESE-3A, Net, ABT1 and ERF. Members of the Ets gene family exhibit varied patterns of tissue expression, and share a highly conserved carboxy terminal domain containing a sequence related to the SV40 large T antigen nuclear localization signal sequence. This conserved domain is essential for Ets-1 binding to DNA and is likely to be responsible for the DNA binding activity of all members of the Ets gene family. Several of these proteins have been shown to recognize similar motifs in DNA that share a centrally located 5'-GGAA-3' element. Function: Functions as a transcriptional regulator. According to PubMed:12761502, it functions as a transcriptional repressor. Functions in贰罢厂结构域转录因子贵贰痴抗体 the differentiation and the maintenance of the central serotonergic neurons. May play a role in cell growth. Subcellular Location: Nucleus. Tissue Specificity: In brain, exclusively expressed in the major serotonergic neurons of the dorsal and median raphe nuclei located in the midbrain and pons. Also detected in prostate and small intestine. DISEASE: Genetic variation in FEV may be associated with susceptibility to sudden infant death syndrome (SIDS) [MIM:272120]. SIDS remains elusive in its causes and devastating in its consequences. Despite the impressive decline in the incidence of SIDS since the recommendation to avoid the prone sleep position, SIDS remains a leading cause of death in the first year贰罢厂结构域转录因子贵贰痴抗体 of life. Note=A chromosomal aberration involving FEV is found in Ewing tumors. Translocation t(2;21;22)(q23;q22;q12) that forms a EWSR1-FEV fusion protein with a potential oncogenic activity. Similarity: Belongs to the ETS family. Contains 1 ETS DNA-binding domain. Database links: Entrez Gene: 54738 Human Omim: 607150 Human SwissProt: Q99581 Human Unigene: 234759 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

贰罢厂结构域转录因子贵贰痴抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 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.

研究领域:肿瘤  神经生物学  转录调节因子  Alzheimer's  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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