Cell Signaling Technology

Product Pathways - Lymphocyte Signaling

PU.1 (9G7) Rabbit mAb #2258

31 kDa transforming protein   p.u.   p.u.1   pu   pu1   sc-352   SPl1   Spleen focus forming virus proviral integration site-1  

No. Size Price
2258S 100 µl ( 10 western blots ) ¥3,100.00 现货查询 购买询价
2258 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse, Endogenous 42 Rabbit IgG
IP 1:100
IHC-P 1:50
F 1:100
IF-IC 1:200
ChIP 1:100

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation, IHC-P=Immunohistochemistry (Paraffin), F=Flow Cytometry, IF-IC=Immunofluorescence (Immunocytochemistry), ChIP=Chromatin IP,


Species predicted to react based on 100% sequence homology: Pig,

Specificity / Sensitivity

This antibody detects endogenous levels of total PU.1 protein. The antibody does not cross react with other Ets family members.


Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the sequence of human PU.1 protein.

此单克隆抗体是通过合成人源对应的 PU.1序列来免疫动物而获得。

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded Non-Hodgkin's lymphoma using PU.1 (9G7) Rabbit mAb in the presence of control peptide (left) or PU.1 Blocking Peptide #1036 (right).免疫组织化学染色分析石蜡包埋人非霍奇金淋巴瘤组织。在对照多肽(左图) 或PU.1 封闭多胎#1036 (右图)存在下用PU.1 (9G7) Rabbit mAb抗体。

Western Blotting

Western Blotting

Western blot analysis of extracts from RAW, THP1 and p388D1 cells using PU.1 (9G7) Rabbit mAb.Western免疫印迹。用PU.1 (9G7) Rabbit mAb研究RAW, THP1 和 p388D1 细胞的细胞提取液。

Flow Cytometry

Flow Cytometry

Flow cytometric analysis of untreated THP-1 cells using PU.1 (9G7) Rabbit mAb (blue) compared to a nonspecific negative control antibody (red).流式细胞仪分析未经处理的THP-1 细胞,所用抗体为PU.1 (9G7) Rabbit mAb (蓝色) 以非特异性抗体为阴性对照(红色)。

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded 4T1 syngeneic mouse tumor using PU.1 (9G7) Rabbit mAb #2258.免疫组织化学染色分析石蜡包埋小鼠同系癌组织。所用抗体为PU.1 (9G7) Rabbit mAb #2258。

Chromatin IP

Chromatin IP

Chromatin immunoprecipitations were performed with cross-linked chromatin from 4 x 106 U-937 cells and either 10 μl of PU.1 (9G7) Rabbit mAb or 2 μl of Normal Rabbit IgG #2729 using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time PCR using human CD11b promoter primers, human CD18 intron 1 primers, and SimpleChIP® Human α Satellite Repeat Primers #4486. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.染色质免疫共沉淀。U-937细胞培养至4 x 106,将染色质交联到玻片上,然后用SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003进行免疫沉淀实验,本实验中用10 μl PU.1 (9G7) Rabbit抗体或2 μl Normal Rabbit IgG #2729 。对富集的DNA做real-time PCR,所用引物为human CD11b promoter primers, human CD18 intron 1 primers和SimpleChIP® Human α Satellite Repeat Primers #4486。每个样本中沉淀的DNA量定义为相对信号与输入的总染色质相比的数值。



Confocal immunofluorescent analysis of Raw cells using PU.1 (9G7) Rabbit mAb (green). Actin filaments were labeled with DY-554 phalloidin (red).


PU.1 is a member of the Ets family of transcription factors and activates target genes through the purine-rich PU-box (1). PU.1 plays a pivotal role in the differentiation of myeloid cells and lymphocytes and is expressed in several hematopoietic cells including B lymphocytes, macrophages, neutrophils, mast cells, early erythroid cells and megakaryocytes (1,2). The concentration of PU.1 is critical for both the determination of hematopoietic cell lineage and the regulation of differentiation versus stem cell proliferation (3,4). In addition, PU.1 activity is influenced by phosphorylation and interactions with other hematopoietic transcription factors. Phosphorylation of PU.1 at Ser146 by CK2 promotes binding to IRF4 and synergistic activation through the immunoglobulin κ 3' enhancer (5). Treatment of pro-B cells with IL-3 leads to phosphorylation of PU.1 at Ser140, resulting in increased PU.1 activity and activation of the anti-apoptotic gene MCL-1 (6). GATA1 binding blocks PU.1 activity during erythroid cell development (7). Overexpression of PU.1 resulting from proviral insertion during Friend virus infection can induce erythroleukemia, while reduced expression has been associated with acute myeloid leukemia (8).

PU.1是转录因子Ets家族中的一员,通过嘌呤富集区域PU-box激活转录目标基因(1)。PU.1在骨髓细胞和淋巴细胞的分化过程中发挥了关键的作用,并在一些骨髓细胞中表达,如 B 淋巴细胞, 巨噬细胞,嗜中性粒细胞,肥大细胞,早期红系细胞和(1,2)。PU.1的浓度对淋巴细胞系的分化和干细胞的分化都有重要的作用(3,4)。另外, PU.1的活性受到磷酸化和造血转录因子互作的影响。PU.1通过CK2在Ser146位点的磷酸化促进了其与IRF4的结合并通过免疫球蛋白 κ 3' 增强子增强了活性(5)。用IL-3处理pro-B细胞导致了PU.1在Ser140位点的磷酸化, 从而增强了PU.1的活性和抗凋亡基因MCL-1的表达(6)。在红系细胞的发育中,GATA1的结合抑制了PU.1活性(7)。过表达PU.1 导致了在Friend病毒入侵时前病毒插入能诱导红白血病 , 而如果降低其表达则与急性的粒细胞性白血病有关(8)。

  1. Lloberas, J. et al. (1999) Immunol Today 20, 184-9.
  2. Klemsz, M.J. et al. (1990) Cell 61, 113-24.
  3. Dahl, R. and Simon, M.C. (2003) Blood Cells Mol Dis 31, 229-33.
  4. DeKoter, R.P. and Singh, H. (2000) Science 288, 1439-41.
  5. Pongubala, J.M. et al. (1993) Science 259, 1622-5.
  6. Wang, J.M. et al. (2003) Mol Cell Biol 23, 1896-909.
  7. Zhang, P. et al. (1999) Proc Natl Acad Sci U S A 96, 8705-10.
  8. Moreau-Gachelin, F. et al. (1988) Nature 331, 277-80.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

U.S. Patent No. 5,675,063.

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.

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