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GloboZymes/PP2A A Subunit/5μg/GLO138-005

价格
¥13740.00
货号:GLO138-005
浏览量:127
品牌:GloboZymes
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商品描述

PP2A A Subunit

Source: Recombinant Human

Purity: > 90% by SDS-PAGE, apparent Mr ~ 65-kDa

Supplied: 1 μg in 50 μl of 50 mM Tis-HCl pH 7.0 buffer containing 0.1 mM phenylmethanesulfonyl fluoride, 14 mM β-mercaptoethanol, 1 mM EDTA and 50% glycerol. Maintain in aliquots at -70°C. Avoid repeated thawing.

Synonyms: Regulatory 65 kDa A Subunit of Protein Phosphatase 2A; PR65

Background: The A PR65 subunit of PP2A serves as a scaffolding molecule to coordinate the assembly of the catalytic (PP2AC) and variable B subunits. This generates functionally diverse heterotrimers of the phosphatase. The A subunit contains 15 tandemly-repeated HEAT sequences which may participate in its function as a scaffolding molecule. The A subunit also serves to regulate the substrate selectivity of PP2AC and allosterically modulates its polycation response. Association of recombinant A subunit with PP2AC is relatively tight (apparent KD ~ 85 pM) and leads to marked suppression of phosphatase activity with several phosphoproteins substrates. By contrast, suppression of PP2A activity is markedly less with several less-structured or smaller substrates such as phosphopeptides. The affinity of the A subunit for PP2AC is diminished by almost 100-fold following introduction of a glutamate at position 416. This indicates that the basic motif in this region of the protein may be important for its interaction with PP2AC. Some evidence indicates a role for the A subunit in disease. For example, at least four low frequency mutations in genes encoding the A subunit with altered affinity for PP2AC have been identified in several different human cancers. Additionally, overexpression of the A subunit in rat embryo fibroblasts leads to multinucleated cells.

References: Eur J Biochem 267: 5209  Eur J Biochem 248: 200

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。