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位置: 首页 > 磷酸化抗体 > eIF4E(Phospho-Ser209) Antibody

eIF4E(Phospho-Ser209) Antibody#11233

eIF4E(Phospho-Ser209) Antibody
eIF4E(Phospho-Ser209) Antibody
eIF4E(Phospho-Ser209) Antibody
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产品总价:
产品详情

产品名称eIF4E(Phospho-Ser209) Antibody

来源种属Rabbit

克隆性Polyclonal

纯化Antibodies were produced by immunizing rabbits with synthetic phosphopeptide and KLH conjugates. Antibodies were purified by affinity-chromatography using epitope-specific phosphopeptide. Non-phospho specific antibodies were removed by chromatogramphy using non-phosphopeptide.

应用WB IHC IF

种属反应性Hu

特异性The antibody detects endogenous level of eIF4E only when phosphorylated at serine 209.

免疫原类型Peptide-KLH

免疫原描述Peptide sequence around phosphorylation site of serine 209 (S-G-S(p)-T-T) derived from Human eIF4E.

基因/蛋白名称eIF4E

修饰Phospho

别名mRNA cap-binding protein; eIF-4F 25 kDa subunit;

数据库入口号Swiss-Prot: P06730
NCBI Protein: NP_001124150.1

浓度1.0mg/ml

配方Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

保存Store at -20°C for long term preservation (recommended). Store at 4°C for short term use.

应用详情

Predicted MW: 25kd
Western blotting: 1:500~1:1000
Immunohistochemistry: 1:50~1:100
Immunofluorescence: 1:100~1:200

Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using eIF4E(Phospho-Ser209) Antibody #11233(left) or the same antibody preincubated with blocking peptide(right).
Immunofluorescence staining of methanol-fixed MCF cells using eIF4E(Phospho-Ser209) Antibody #11233.
Western blot analysis of extracts from SK-BR-3 cells, untreated or insulin and EGF treated, and pretreated with U0126 cells, using eIF4E (Phospho-Ser209) Antibody #11233.
背景

Recognizes and binds the 7-methylguanosine-containing mRNA cap during an early step in the initiation of protein synthesis and facilitates ribosome binding by inducing the unwinding of the mRNAs secondary structures.

Li BD, et al. (1998) Ann Surg; 227(5): 756-763
Altmann M, et al. (1989) Nucleic Acids Res; 17(18): 7520
De Gregorio E, et al. (2001) RNA; 7(1): 106-113
Gu W, et al. (2004) Nucleic Acids Res; 32(15): 4448-4461

如果您使用该产品11233发表了文章,请通知我们,让我们可以引用您的文献。

et al,Conversion of Leucine to 尾-Hydroxy-尾-Methylbutyrate by 伪-Keto Isocaproate Dioxygenase Is Required for a Potent Stimulation of Protein Synthesis in L6 Rat Myotubes.In J Cachexia Sarcopenia Muscle on 2016 Mar by Mar铆a D Gir贸n , Jos茅 D V铆lchez et al..PMID:27065075, , (2016),
PMID: 27065075
et al,Activation of ERK by sodium tungstate induces protein synthesis and prevents protein degradation in rat L6 myotubes.In FEBS Lett on 2014 Jun 27 by Rafael Salto, Jos茅 D V铆lchez et al..PMID:24846141 , , (2014),
PMID: 24846141
5

注释

应用

  • WB免疫印迹
  • IHC免疫组化
  • IF免疫荧光
  • ICC免疫细胞化学
  • FC流式细胞
  • IP免疫沉淀
  • E酶联免疫吸附法
  • DB免疫斑点法
  • ChIP染色质免疫沉淀
  • GICA胶体金免疫层析法
  • NC阴性对照

种属反应性

  • Hu
  • Ms小鼠
  • Rt大鼠
  • Dm果蝇
  • C线虫
  • Mk
  • Rb
  • B
  • D
  • P
  • Hm仓鼠
  • ChHm中国仓鼠
  • Chk

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