Erk1/2 Recombinant Rabbit mAb (S-3178)
Mitogen-activated protein kinase 1,MAP kinase 1,MAPK 1,ERT1,Extracellular signal-regulated kinase 2 (ERK-2),MAP kinase isoform p42 (p42-MAPK),Mitogen-activated protein kinase 2 (MAP kinase 2,MAPK 2),ERK2,PRKM1,PRKM2,MAPK1
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宿主来源
Rabbit抗原名称
Erk1/2分子别名
Mitogen-activated protein kinase 1; MAP kinase 1; MAPK 1; ERT1; Extracellular signal-regulated kinase 2 (ERK-2); MAP kinase isoform p42 (p42-MAPK); Mitogen-activated protein kinase 2 (MAP kinase 2; MAPK 2); ERK2; PRKM1; PRKM2; MAPK1细胞定位
Cytoskeleton, Nucleus, CytoplasmAccession
P28482克隆号
S-3178抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms, Rt阳性样本
HeLa, K562, Daud, HepG2, U-87 MG, PC-3, NIH/3T3, C6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
ICFCM ,IHC-P ? ,ICC ? ,WB稀释度
应用 稀释度 推荐种属 WB 1:1000-1:5000 Hu, Ms, Rt, Mk IHC-P 1:500 Hu, Ms, Rt ICC 1:500 Hu ICFCM 1:500 Hu
Erk1/2 proteins, also known as extracellular signal-regulated kinases 1 and 2, are key components of the MAPK (mitogen-activated protein kinase) signaling pathway. They play roles crucial in regulating various cellular processes such as cell proliferation, differentiation, survival, and apoptosis. Erk1/2 can be activated by a wide range of extracellular stimuli including growth factors, cytokines, and hormones. Once activated, they phosphorylate a cascade of downstream targets, thereby transmitting signals from the cell surface to the nucleus and modulating gene expression. Dysregulation of Erk1/2 signaling has been implicated in numerous diseases, including cancer andde neurogenerative disorders, making them important targets for therapeutic intervention.
免疫印迹
WB result of Erk1/2 Recombinant Rabbit mAb
Primary antibody: Erk1/2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: K562 whole cell lysate 20 µg
Lane 3: Daudi whole cell lysate 20 µg
Lane 4: HepG2 whole cell lysate 20 µg
Lane 5: U-87 MG whole cell lysate 20 µg
Lane 6: PC-3 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 40 kDaWB result of Erk1/2 Recombinant Rabbit mAb
Primary antibody: Erk1/2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: NIH/3T3 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39, 42 kDaWB result of Erk1/2 Recombinant Rabbit mAb
Primary antibody: Erk1/2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: C6 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39, 42 kDaWB result of Erk1/2 Recombinant Rabbit mAb
Primary antibody: Erk1/2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: COS-7 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 40 kDa
流式分析
Flow cytometric analysis of 4% PFA fixed 90% methanol permeabilized U-87 MG (Human glioblastoma-astrocytoma epithelial cell) labelling Erk1/2 antibody at 1/500 dilution (0.1 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.
免疫组化
IHC shows positive staining in paraffin-embedded human kidney. Anti-Erk1/2 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human breast cancer. Anti-Erk1/2 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human lung cancer. Anti-Erk1/2 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded mouse cerebral cortex. Anti-Erk1/2 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded rat stomach. Anti-Erk1/2 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
免疫细胞化学
ICC shows positive staining in U-87 MG cells. Anti-ERK1/2 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 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
组织表达图谱
Expression of Erk1/2 in tumor tissue.
Expression of Erk1/2 in human tissue.
Expression of Erk1/2 in mouse & rat tissue.
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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