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GloboZymes/I1PP2A Detection Kit/GLO149-01

价格
¥13120.00
货号:GLO149-01
浏览量:127
品牌:GloboZymes
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商品描述

I1PP2A Detection Kit

GloboZymes I1PP2A Detection Kit includes 100 μg affinity-purified rabbit Anti-I1PP2A polyclonal antibody and an aliquot of highly purified I1PP2A. The aliquot is provided in SDS sample buffer ready for use in five applications as positive control in Western blots. The polyclonal antibody was produced in rabbits to a synthetic peptide corresponding to residues 149-163 of human kidney I1PP2A.

Synonyms: Protein Phosphatase 2A Inhibitor Protein 1 Western Blot Detection Kit; Anti-I1 Detection Kit; I1PP2A is also termed: I1PP2A, PHAP-I, p32/33 and LANP.

Background: The PP2A inhibitor proteins, I1PP2A and I2PP2A, were discovered by GloboZymes founder Dr. Zahi Damuni during his tenure as professor at The Pennsylvania State University College of Medicine. Numerous laboratories around the world have since demonstrated further the significance of these proteins including in various diseases such as cancer and alzheimers. Purified preparations of I1PP2A inhibit all forms of protein phosphatase 2A (PP2A) tested to date in a substrate-selective manner. The purified preparations inhibit PP2A potently (ki ~ 0.1 – 0.5 nM) with Myelin Basic Protein (MBP) and Histone H1 but not with Casein as substrate. In contrast, I1PP2A stimulates PP1 activity in the presence of Mn2+. In cells, I1PP2A undergoes phosphorylation on serine and tyrosine residues. The functional significance of the serine phosphorylations is unclear. Tyrosine phsophorylation of I1PP2A occurs in response to the antiproliferative lectin Jacalin. It causes the dissociation of the I1PP2A PP2A complex, with the concomitant activation of the phosphatase.

Figure: Western Blot of a purified preparation of I1PP2A with Anti-I1PP2A.

References:  Li M, Makkinje A, Damuni Z. (1996) Biochemistry 35, 6998-7002; Vaesen, M. et al (1994) Biol Chem Hoppe Seyler 375, 113-126; Malek, S. N. et al (1990) J Biol Chem 265, 13400-13409; Li, M., Damuni, Z. (1998) Methods Mol Biol  93, 59-66; Katayose, Y. et al (2000) J Biol Chem 275, 9209-9214; Yu L-G et al (2004) J Biol Chem 279, 41377-41383

GloboZymes的eIF4E(S53A)来源:在大肠杆菌中产生的重组人 纯度:通过SDS-PAGE大于90%,表观先生〜28-kDa提供:在50μl的50 mM Tris-HCl pH 7.0缓冲液中,其中含有14 mMβ-巯基乙醇,1 mM苯甲am,0.1 mM苯基甲磺酰氟,1 mM EDTA和10%甘油。等分试样保持在-70°C下。避免重复解冻。别名:丙氨酸突变体的真核蛋白合成起始因子4E丝氨酸53;eIF-4E S53A。eIF4ES53A背景:mRNA Cap结合蛋白合成起始因子4E(eIF4E)参与了蛋白合成的早期限速步骤。eIF4E的过表达导致细胞转化和肿瘤发生,并发生在许多癌细胞中。在静止细胞中,eIF4E作为与4EBP结合蛋白的非活性复合物存在。响应胰岛素和其他细胞外刺激,eIF4E与4EBP分离并被募集到活性eIF4F复合体中。活性eIF4F复合体除eIF4E外还包含eIF4A和eIF4G。响应胰岛素和其他生长因子,eIF4E在Ser209处被磷酸化。这种磷酸化增强了eIF4E对加帽的mRNA的亲和力。它是由丝裂素激活的蛋白激酶(MAPK)相互作用激酶(Mnk's)催化的。它也被称为cPK的胰岛素刺激的激酶催化,该激酶也使Thr210在起始因子上磷酸化。 图:纯化的eIF4E(S53A)制剂的SDS-PAGE模式。凝胶用考马斯蓝染色。