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当前位置:首页 > 抗原抗体、ELISA、WB > 一抗 > Polyclonal Antibodies > Runx1/AML1-ETO polyclonal antibody

Runx1/AML1-ETO polyclonal antibody

货号 货期 规格 / 价格 询价
APR00371G 50 μl / ¥4950

Runx1/AML1-ETO polyclonal antibody

品牌

Leading Biology

货号

APR00371G

产品分类

Polyclonal Antibodies

研究领域

产品概述

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Runx1/AML1-ETO polyclonal antibody.

分子量

48737 Da

细胞定位

Antigen Cellular Localization: Nucleus.

宿主

Rabbit

靶点

Runx1/AML1-ETO

亚型

Rabbit IgG

通用名

AML1, CBFA2

基因ID

UniProt ID

功能

CBF binds to the core site, 5'-PYGPYGGT-3', of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, LCK, IL-3 and GM-CSF promoters. The alpha subunit binds DNA and appears to have a role in the development of normal hematopoiesis. Isoform AML-1L interferes with the transactivation activity of RUNX1. Acts synergistically with ELF4 to transactivate the IL-3 promoter and with ELF2 to transactivate the mouse BLK promoter. Inhibits KAT6B- dependent transcriptional activation.

总结

This antibody specifically recognizes the AML1 (RUNX1) - ETO (RUNX1T1) fusion protein that arises due to a translocation between chromosome 8 and 22 (t(8;21)(q22;q22)). This translocation is one of the most frequent karyotypic abnormalities observed in acute myeloid leukemia. It produces a chimerical gene made up of the 5’-region of AML1and the 3’-region of ETO. The chimerical protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation.

形式

Liquid

储存条件

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

应用

WB, E

图像

ChIP assays were performed using Kasumi cells and the antibody and optimized PCR primer sets for qPCR. The Fig shows the occupancy, calculated as the ratio + control/background for which the promoter of the H2B gene was used.

To determine the titer, an ELISA was performed using a serial dilution of the antibody. The antigen used was a peptide containing the histone modification of interest. By plotting the absorbance against the antibody dilution the titer of the antibody was estimated to be 1:32,750.

说明书

数量

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