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Merck
所有图片(6)

主要文件

05-1003

Sigma-Aldrich

抗磷酸化-Akt(Ser473)抗体,克隆6F5

clone 6F5, from mouse

别名:

Protein kinase B, RAC-alpha serine/threonine-protein kinase, murine thymoma viral (v-akt) oncogene homolog-1, rac protein kinase alpha, v-akt murine thymoma viral oncogene homolog 1

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About This Item

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物来源

mouse

质量水平

抗体形式

purified antibody

抗体产品类型

primary antibodies

克隆

6F5, monoclonal

种属反应性

rat, mouse, vertebrates, human

技术

ELISA: suitable
flow cytometry: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
western blot: suitable

同位素/亚型

IgG1κ

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

phosphorylation (pSer473)

基因信息

human ... AKT1(207)
rat ... Akt1S1(292887)

一般描述

Akt/PKB是Ser/Thr激酶,是PI3激酶途径的主要已知效应子。 它参与与许多生物学过程有关的多种信号传导途径,包括葡萄糖代谢,细胞存活/凋亡,细胞周期控制,血管生成,分化以及细胞生长和增殖。 在哺乳动物中,存在Akt的三种亚型(Akt1/PKB;Akt2/PKB;Akt3/PKB)。 它们表现出高度的同源性,但在其调节磷酸化位点的定位上略有不同。Akt是大多数组织中的主要亚型,被认为在生长,存活,胚胎发育和脂肪细胞分化中起主要作用。Akt2与葡萄糖稳态的调节相关,并且是在胰岛素反应性组织中表达的主要亚型。 Akt3在脑组织中含量丰富。每个Akt亚型由三个功能上不同的区域组成:一个N末端Pleckstrin同源性(PH)域,该域提供了一个脂质结合模块,可将Akt引导至激活其所必需的细胞膜上的PIP3,一个包含Thr308的中央催化域,以及包含Ser473的C端疏水基序。 Akt的激活取决于双重调节机制,该机制既需要将其转运至质膜,又需要分别通过PDK1和TORC2复合物在Thr308和Ser473上进行双重磷酸化。

特异性

仅在Ser473磷酸化后可识别Akt。当Akt1/PKB在Ser473上未磷酸化时,该抗体不与Akt1/PKBα发生交叉反应。
预期与大多数物种反应,因为该序列与大多数常见脊椎动物的同源性为100%。

免疫原

包含并包括人Akt1磷酸化Ser473的肽。

应用

免疫荧光分析:
μ将EGF处理的A431细胞固定,透化并用抗磷酸化Akt(Ser473),克隆6F5(2 g/ml)(红色)染色。使用Cy3偶联的抗小鼠进行检测,并使用鬼笔环肽-AlexaFluor488(绿色)对肌动蛋白染色。

免疫组织化学:
将抗磷酸化Akt(Ser473),克隆6F5稀释至1:200,用HRP-DAB进行IHC-Select检测。

流式细胞术:
抗磷酸化Akt(Ser473)以1:800的稀释度用于该测定。
抗-磷酸化-Akt(Ser473)抗体,克隆6F5,检测磷酸化-Akt(Ser473)的水平,&已发布,&经过验证可用于ELISA、WB、FC、IF、IH。

质量

蛋白质印迹分析:
0.5-1 μg/mL该批次在用100 ng/mL PDGF处理20分钟的小鼠NIH-3T3成纤维细胞的裂解液中检测到磷酸化的Akt。

目标描述

60 kDa

外形

形式:纯化
纯化的小鼠单克隆IgG1κ,溶于0.1M Tris-甘氨酸(pH 7.4),150mM NaCl和0.05%NaN3中

其他说明

浓度:请参考批次特异性浓缩物的分析证书。

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

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Xiaoli Li et al.
The Journal of biological chemistry, 290(5), 2715-2727 (2014-12-17)
Functional maintenance of hematopoietic stem cells (HSCs) is constantly challenged by stresses like DNA damage and oxidative stress. Here we show that the Fanconi anemia protein Fancd2 and stress transcriptional factor Foxo3a cooperate to prevent HSC exhaustion in mice. Deletion
Zhicheng Liu et al.
Discover. Oncology, 13(1), 8-8 (2022-02-25)
Colorectal cancer (CRC) is considered to be a leading cause of cancer-related death. Centromere protein O (CENPO) can prevent the separation of sister chromatids and cell death after spindle injury. Nevertheless, the role of CENPO in CRC has not been
Paula J S Pereira et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 35(49), 16272-16281 (2015-12-15)
The gastrin-releasing peptide (GRP) and its receptor (GRPR) are important components of itch transmission. Upstream, but not downstream, aspects of GRPR signaling have been investigated extensively. We hypothesize that GRPR signals in part through the PI3Kγ/Akt pathway. We used pharmacological
Yanru Wang et al.
BioMed research international, 2021, 6685493-6685493 (2021-03-23)
The vascular injury induced by central venous catheter (CVC) indwelling is the basis for the occurrence and development of CVC-related complications, such as phlebitis, venous thrombosis, and catheter-related infections. Focal adhesion kinase (FAK) and FAK-protein kinase B (AKT) signaling pathway
Claire Marceaux et al.
Journal of cell science, 131(5) (2018-02-09)
ARHGAP19 is a hematopoietic-specific Rho GTPase-activating protein (RhoGAP) that acts through the RhoA/ROCK pathway to critically regulate cell elongation and cytokinesis during lymphocyte mitosis. We report here that, during mitosis progression, ARHGAP19 is sequentially phosphorylated by the RhoA-activated kinases ROCK1

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