RUNX1 (Acetyl Lys24) Rabbit Polyclonal Antibody

alternative products:Additional isoforms seem to exist|The fusion of AML1 with EAP in T-MDS induces a change of reading frame in the latter resulting in 17 AA unrelated to those of EAP.|disease:A chromosomal aberration involving RUNX1/AML1 is a cause of chronic myelogenous leukemia (CML). Translocation t(3;21)(q26;q22) with EAP| MSD1 or EVI1.|disease:A chromosomal aberration involving RUNX1/AML1 is a cause of chronic myelomonocytic leukemia. Inversion inv(21)(q21;q22) with USP16.|disease:A chromosomal aberration involving RUNX1/AML1 is a cause of M2 type acute myeloid leukemia (AML-M2). Translocation t(8;21)(q22;q22) with RUNX1T1/MTG8/ETO.|disease:A chromosomal aberration involving RUNX1/AML1 is a cause of therapy-related myelodysplastic syndrome (T-MDS). Translocation t(3;21)(q26;q22) with EAP| MSD1 or EVI1.|disease:A chromosomal aberration involving RUNX1/AML1 is found in childhood acute lymphoblastic leukemia (ALL). Translocation t(12;21)(p13;q22) with TEL. The translocation fuses the 3'-end of TEL to the alternate 5'-exon of AML-1H.|disease:A chromosomal aberration involving RUNX1/AML1 is found in therapy-related myeloid malignancies. Translocation t(16;21)(q24;q22) that forms a RUNX1-CBFA2T3 fusion protein.|disease:Defects in RUNX1 are the cause of familial platelet disorder with associated myeloid malignancy (FPDMM)

The RUNX1 (Acetyl Lys24) Rabbit Polyclonal Antibody is a highly specific and reliable tool designed for the detection and analysis of the RUNX1 protein. This antibody has been meticulously developed using advanced techniques to ensure exceptional performance and accuracy in various applications, including Western blotting, immunohistochemistry, and immunofluorescence.

The RUNX1 protein plays a crucial role in the regulation of gene expression and is involved in hematopoiesis and embryonic development. The acetylation of Lys24 residue on the RUNX1 protein has been shown to have significant implications in its function and activity. This antibody has been specifically designed to target and detect the acetylated form of the Lys24 residue, enabling researchers to gain valuable insights into the molecular mechanisms and biological functions of the RUNX1 protein.

Manufactured with the highest standards of quality, this rabbit polyclonal antibody exhibits exceptional sensitivity and specificity, ensuring reliable and reproducible results. It has been extensively validated in various experimental conditions and has demonstrated excellent performance in detecting the acetylated Lys24 residue of the RUNX1 protein.

The RUNX1 (Acetyl Lys24) Rabbit Polyclonal Antibody is supplied in a convenient and ready-to-use format, allowing for easy integration into laboratory workflows. It is provided in a liquid formulation, ensuring ease of handling and minimizing the risk of sample contamination. The antibody is available in different sizes to accommodate various experimental needs.

With its exceptional specificity, sensitivity, and reliability, the RUNX1 (Acetyl Lys24) Rabbit Polyclonal Antibody is an indispensable tool for researchers studying the role of the RUNX1 protein in various biological processes. Its high-quality performance and versatility make it an ideal choice for a wide range of applications, facilitating groundbreaking discoveries and advancements in the field of molecular biology and biomedical research.