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宿主来源
Mouse抗原名称
PU.1分子别名
Transcription factor PU.1; SPI1细胞定位
NucleusAccession
P17947克隆号
S-4307抗体类型
Mouse mAb抗体同种型
IgG2a反应种属 ?
Hu阳性样本
Human PBMC纯化方式
Protein A浓度
2 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4
储存条件
12 months from date of receipt / reconstitution, 2 to 8 °C as supplied
应用
ICFCM
稀释度
应用 稀释度 推荐种属 ICFCM 1:2000 Hu
PU.1, also known as SPI1 (Spleen Focus Forming Virus Proviral Integration Oncogene), is a critical ETS-family transcription factor that serves as a master regulator of hematopoiesis, specifically governing the development, differentiation, and functional maturation of myeloid lineages (including monocytes, macrophages, and granulocytes) and B lymphocytes. Functioning by binding to specific purine-rich DNA sequences via its highly conserved ETS domain, PU.1 orchestrates complex gene regulatory networks by recruiting co-activators or co-repressors to control the expression of hundreds of target genes essential for immune cell identity, such as those encoding cytokine receptors, signaling molecules, and lineage-specific enzymes; its activity is tightly dosage-dependent, where precise expression levels determine cell fate decisions, with high levels promoting macrophage differentiation and lower levels favoring B-cell development, while its dysregulation, mutation, or aberrant overexpression is strongly implicated in various hematological malignancies, particularly acute myeloid leukemia (AML) and certain types of lymphoma, making it a pivotal molecule for understanding both normal immune system architecture and leukemogenesis.
流式分析
Flow cytometric analysis of PU.1 expression in PBMC (Human peripheral blood mononuclear cells). Human PBMC were fixed and permeabilized with Foxp3 / Transcription Factor Staining Buffer Set. The cells were then labeled with Human PU.1 antibody at 1/2000 dilution (0.1 μg) / (right panel) compared with a Mouse IgG2a Isotype Control / (left panel). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD19 - PE-Cy7 antibody separately. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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