Phospho-PKR (Thr446) Recombinant Rabbit mAb (S-771-17)
Interferon-induced,double-stranded RNA-activated protein kinase,Eukaryotic translation initiation factor 2-alpha kinase 2 (eIF-2A protein kinase 2),Interferon-inducible RNA-dependent protein kinase,P1/eIF-2A protein kinase,Protein kinase RNA-activated (PKR,Protein kinase R),Tyrosine-protein kinase EIF2AK2,p68 kinase,PKR,PRKR,EIF2AK2
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宿主来源
Rabbit抗原名称
Phospho-PKR (Thr446)分子别名
Interferon-induced, double-stranded RNA-activated protein kinase; Eukaryotic translation initiation factor 2-alpha kinase 2 (eIF-2A protein kinase 2); Interferon-inducible RNA-dependent protein kinase; P1/eIF-2A protein kinase; Protein kinase RNA-activated (PKR; Protein kinase R); Tyrosine-protein kinase EIF2AK2; p68 kinase; PKR; PRKR; EIF2AK2免疫原
Synthetic Peptide细胞定位
Nucleus, CytoplasmAccession
P19525克隆号
S-771-17抗体类型
Recombinant mAb抗体同种型
IgG翻译后修饰类型
磷酸化反应种属 ?
Hu纯化方式
Protein A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
应用
ICC ?
WB
稀释度
应用 稀释度 推荐种属 Dot Blot 1:1000 WB 1:500 Hu ICC 1:100 Hu
Protein Kinase R (PKR), also known as double-stranded RNA-dependent protein kinase, is a key enzyme involved in the innate immune response to viral infections. It is an interferon-induced, serine/threonine protein kinase that becomes activated upon binding to double-stranded RNA (dsRNA), which is often produced during viral replication. Once activated, PKR phosphorylates the eukaryotic initiation factor 2α (eIF-2α), inhibiting protein synthesis and thus limiting viral replication. Additionally, PKR plays roles in regulating apoptosis, cell growth, and differentiation, and has been implicated in cancer and metabolic diseases. Its versatile functions make it a significant target for therapeutic research.
免疫印迹
WB result of Phospho-PKR (Thr446) Recombinant Rabbit mAb
Primary antibody: Phospho-PKR (Thr446) Recombinant Rabbit mAb at 1/500 dilution
Lane 1: untreated HeLa whole cell lysate 20 µg
Lane 2: HeLa treated with 100 ng/ml Calyculin A for 30 minutes and 20 ng/ml TNF-α for 5 minutes whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 62 kDa
Observed MW: 70 kDa
斑点杂交
Dot blot result of Phospho-PKR (Thr446) Recombinant Rabbit mAb
Lane 1: PKR (Thr446) phospho peptide
Lane 2: PKR (Thr446) unmodified peptide
Primary antibody: Phospho-PKR (Thr446) Recombinant Rabbit mAb at 1/1000 dilution
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
免疫细胞化学
ICC analysis of HeLa cells treated with Calyculin A (100ng/ml, 30min) and TNF-α (20ng/ml, 5min) (top panel) and untreated HeLa cells (below panel). Anti- Phospho-PKR (Thr446) antibody was used at 1/100 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
我们推荐客户使用TPST+5%脱脂奶粉来稀释一抗,进行封闭。 虽然BSA被推荐为WB检测磷酸化蛋白的常用封闭剂,但是脱脂奶粉获取更加方便,覆盖更广泛的非特异性结合位点,在一抗性能优越的前提下,使用脱脂奶粉封闭性价比更高







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