- 询价
- Signalway Antibody
- USA
- 12890
- 2025年06月29日
- WB
- Rabbit
- Hu Ms Rt
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
A synthesized peptide derived from human IRE1 (Phospho-Tyr166)
- 形态：
liquid
- 保存条件：
Store at -20˚C
- 克隆性：
Polyclonal
- 适应物种：
Hu Ms Rt
- 宿主：
Rabbit
- 应用范围：
WB
- 浓度：
1mg/ml
- 抗体英文名：
IRE1 (Phospho-Tyr166) Antibody
clonality:Polyclonal
specificity:IRE1 (phospho Y166) Antibody detects endogenous levels of IRE1 only when phosphorylated at Y166
other_names:Endoplasmic reticulum (ER) to nucleus signalling 1 antibody Endoplasmic reticulum to nucleus signaling 1 antibody Endoplasmic reticulum-to-nucleus signaling 1 antibody Endoribonuclease antibody ER to nucleus signaling 1 antibody ERN 1 antibody Ern1 antibody ERN1_HUMAN antibody hIRE 1p antibody hIRE1p antibody Inositol requiring 1 antibody Inositol requiring 1 S. cerevisiae homolog of antibody Inositol requiring enzyme 1 S. cerevisiae homolog of antibody Inositol requiring protein 1 antibody inositol-requiring enzyme 1 antibody Inositol-requiring protein 1 antibody IRE 1 antibody IRE 1a antibody IRE 1P antibody Ire1 alpha antibody Ire1-alpha antibody IRE1a antibody Ire1alpha antibody IRE1P antibody MGC163277 antibody MGC163279 antibody Protein kinase endoribonuclease antibody RGD1559716 antibody Serine threonine protein kinase endoribonuclease IRE1 antibody
accession_no:Swiss-Prot#:O75460/Q76MJ5
NCBI Gene ID2081/10595
产品详细信息请点击：IRE1 (Phospho-Tyr166) Antibody
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文献和实验运用Cell Based Elisa检测信号通路蛋白和磷酸化蛋白
using Phospho-p38 antibody (A) and Total-p38 antibody (B). Cell Based Elisa were performed directly in the 96-well plates using Phospho-p38 and Total-p38 antibodies (C). Figure 3: JNK detection with FACECells were serum-starved for 16 hours
。所以，我们建议使用微波炉或高压锅加热煮沸以达到最佳抗原修复效果。抗体：Phospho–Stat3 (Tyr705)(D3A7) XP. Rabbit mAb #9145样本：石蜡包埋人类肺部肿瘤样本煮沸设备：浴锅 (左)，微波炉 (中)，高压锅 (右)免疫染色—封闭在 IHC–P 中，我们建议在室温下在含有 Tween20 的 TBST 缓冲液和 5% 正常山羊血清 (NGS) 中封闭样品，时长 1 小时，以防止非特异性背景染色。在进行 IHC–F 时，在含有 0.3% Triton. X–100 的 1X
v468. chapter 4 WNT 细胞通路 检测细胞GSK3活性与表达水平
. Immunoblot using antibodies to phospho-Tyr279/216 can assess alterations in activity independent ofthe N-terminal phosphorylation, although phosphorylation atthis site is most likely to be constitutive (14) . 3. Immunoblot using antibodies to known
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