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Rabbit抗原名称
4E-BP1分子别名
Eukaryotic translation initiation factor 4E-binding protein 1; 4E-BP1; eIF4E-binding protein 1; Phosphorylated heat- and acid-stable protein regulated by insulin 1 (PHAS-I); EIF4EBP1免疫原
Synthetic Peptide细胞定位
Cytoplasm, NucleusAccession
Q13541克隆号
S-4103-65抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms, Rt, Mk阳性样本
Raji, HepG2, HeLa, MCF7, C2C12, NIH/3T3, mouse skeletal muscle, rat skeletal muscle, COS-7预测反应种属
(反应种属缩写表)/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
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 1:1000 Hu ICC 1:500 Ms
4E-BP1 (eukaryotic initiation factor 4E-binding protein 1) is a key regulator of protein translation and plays a crucial role in controlling the assembly of the eIF4F complex, which is essential for cap-dependent translation initiation. It is the most widely expressed and well-characterized member of the 4E-BP family in mammalian cells. When active, 4E-BP1 binds to eIF4E, preventing its interaction with eIF4G and thereby inhibiting the formation of the eIF4F complex, which is necessary for the translation of many oncogenic mRNAs with structured 5′-UTRs. This mechanism is critical in suppressing tumor development, as hyperactive eIF4E-dependent translation contributes to the upregulation of pro-tumorigenic genes in cancer cells. The activity of 4E-BP1 is regulated by various signaling pathways, including the PI3K/AKT/mTOR pathway, which can lead to its phosphorylation and inactivation, allowing eIF4E to promote translation. Reactivating 4E-BP1 through mTOR inhibition or other mechanisms has been shown to have tumor-suppressive effects.
免疫印迹
WB result of 4E-BP1 Recombinant Rabbit mAb
Primary antibody: 4E-BP1 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: Raji whole cell lysate 20 µg
Lane 2: HepG2 whole cell lysate 20 µg
Lane 3: HeLa whole cell lysate 20 µg
Lane 4: MCF7 whole cell lysate 20 µg
Low expression control: Raji whole cell lysate
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDaWB result of 4E-BP1 Recombinant Rabbit mAb
Primary antibody: 4E-BP1 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: C2C12 whole cell lysate 20 µg
Lane 2: NIH/3T3 whole cell lysate 20 µg
Lane 3: mouse skeletal muscle lysate 20 µg
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDaWB result of 4E-BP1 Recombinant Rabbit mAb
Primary antibody: 4E-BP1 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: rat skeletal muscle lysate 20 µg
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDaWB result of 4E-BP1 Recombinant Rabbit mAb
Primary antibody: 4E-BP1 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: 13 kDa
Observed MW: 15-20 kDa
免疫组化
IHC shows positive staining in paraffin-embedded human kidney. Anti-4 E-BP1antibody was used at 1/1000 dilution, followed by a HRP Polymer for 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 colon cancer. Anti-4 E-BP1antibody was used at 1/1000 dilution, followed by a HRP Polymer for 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 squamous cell carcinoma. Anti-4 E-BP1antibody was used at 1/1000 dilution, followed by a HRP Polymer for 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 NIH/3T3 cells. Anti-4E-BP1 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 4% PFA 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 4E-BP1 in tumor tissues.
Expression of 4E-BP1 in human tissues.
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