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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同型对照
S0B8029反应种属 ?
Hu纯化方式
Protein A浓度
0.2 mg/ml标记
Alexa Fluor® 488性状
Liquid缓冲体系
PBS, 1% BSA, 0.3% Proclin 300
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 5μl per million cells in 100μl volume 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 4% PFA fixed 90% methanol permeabilized THP-1(human monocytic leukemia monocyte, right) or HeLa (Human cervix adenocarcinoma epithelial cell, left) labelling SDT Alexa Fluor® 488 Mouse Anti-Human PU.1 Antibody (red line histogram) at 5 μl/test compared with Alexa Fluor® 488 Mouse IgG2a Isotype Control (black line histogram), cells without incubation with primary antibody and secondary antibody (blue line histogram) was used as unlabeled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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