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Human Monoclonal PRDM1 Primary Antibody for ChIP, ELISA - ABIN153174
John, Clements, Russell, Garrett-Sinha: Ets-1 regulates plasma cell differentiation by interfering with the activity of the transcription factor Blimp-1. in The Journal of biological chemistry 2008
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Human Monoclonal PRDM1 Primary Antibody for ELISA, IHC (fro) - ABIN314190
Liu, Leboeuf, Shi, Li, Wang, Shen, Garcia, Shen, Chen, Janin, Chen, Zhao: Rituximab plus CHOP (R-CHOP) overcomes PRDM1-associated resistance to chemotherapy in patients with diffuse large B-cell lymphoma. in Blood 2007
Show all 11 Pubmed References
Human Monoclonal PRDM1 Primary Antibody for ELISA, ICC - ABIN314189
Ohinata, Payer, OCarroll, Ancelin, Ono, Sano, Barton, Obukhanych, Nussenzweig, Tarakhovsky, Saitou, Surani: Blimp1 is a critical determinant of the germ cell lineage in mice. in Nature 2005
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Human Monoclonal PRDM1 Primary Antibody for ICS, IHC (p) - ABIN2688853
Chan, Chiang, Tsai, Su, Chen, Hou, Lin: Absence of the transcriptional repressor Blimp-1 in hematopoietic lineages reveals its role in dendritic cell homeostatic development and function. in Journal of immunology (Baltimore, Md. : 1950) 2009
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Human Monoclonal PRDM1 Primary Antibody for IHC, WB - ABIN2668849
Valer Corellano: [Malignant fibrous histiocytoma of soft tissues: early report of 10 cases]. in Medicina clínica 1991
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Human Monoclonal PRDM1 Primary Antibody for ELISA, WB - ABIN1724737
Ancelin, Lange, Hajkova, Schneider, Bannister, Kouzarides, Surani: Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells. in Nature cell biology 2006
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Human Polyclonal PRDM1 Primary Antibody for FM, ELISA - ABIN1001904
Angelin-Duclos, Cattoretti, Lin, Calame: Commitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo. in Journal of immunology (Baltimore, Md. : 1950) 2000
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Human Polyclonal PRDM1 Primary Antibody for IHC, ELISA - ABIN1001905
Martins, Cimmino, Shapiro-Shelef, Szabolcs, Herron, Magnusdottir, Calame: Transcriptional repressor Blimp-1 regulates T cell homeostasis and function. in Nature immunology 2006
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Human Polyclonal PRDM1 Primary Antibody for - ABIN2017609
Oestreich, Mohn, Weinmann: Molecular mechanisms that control the expression and activity of Bcl-6 in TH1 cells to regulate flexibility with a TFH-like gene profile. in Nature immunology 2012
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Human Monoclonal PRDM1 Primary Antibody for FACS - ABIN4256285
Joo, Li, Dullaers, Kim, Duluc, Upchurch, Xue, Zurawski, Le Grand, Liu, Kuroda, Zurawski, Oh: C-type lectin-like receptor LOX-1 promotes dendritic cell-mediated class-switched B cell responses. in Immunity 2014
BLIMP1 (PRDM1)expression begins throughout the hypoblast at stage 1 and emerges in single primordial germ cell (PGC (显示 PGC 抗体)) precursors in the posterior epiblast at stage 2.
The timing of shade expression is determined by its transcriptional activator betaFtz-f1. The betaftz-f1 gene is activated after a decline in the expression of its transcriptional repressor Blimp-1.
Blimp-1 gene is transcribed during prepupal development when the ecdysteroid titer is high, but the expressed mRNA degrades rapidly.
Blimp-1 regulates terminal differentiation of the tracheal system in the Drosophila embryo.
These results suggest that the transient transcriptional repressor dBlimp-1 is important for determining developmental timing in the ecdysone-induced pathway.
Expression of the M- and N-cadherins, previously implicated in driving adaxial cell migration, is largely unaffected by loss of Prdm1a function, suggesting that differential cadherin expression is not sufficient for adaxial cell migration
Prdm1a functions as both a transcriptional activator and repressor during neural crest development.
identify sox6 cis (显示 CISH 抗体)-regulatory sequences that drive fast-twitch-specific expression in a Prdm1a-dependent manner
prdm1a expression is upregulated in the absence of Notch (显示 NOTCH1 抗体) function, and inhibiting Notch (显示 NOTCH1 抗体) signaling fails to rescue prdm1a mutants
prdm1a Regulates sox10 (显示 SOX10 抗体) and islet1 (显示 ISL1 抗体) in the development of neural crest and Rohon-Beard sensory neurons.
These results indicate an essential role for prdm1a in the development of the zebrafish craniofacial skeleton.
Here we show that the gene u-boot (ubo), a mutation in which disrupts the induction of embryonic slow-twitch fibers, encodes the zebrafish homolog of Blimp-1
The transcriptional regulator Blimp-1 plays a role in the inception of Neural Crest progenitor fate through BMP signalling.
prdm1/blimp1 has roles in embryo patterning and organogenesis
prdm1 functions to promote the cell fate specification of both neural crest cells and sensory neurons
SOX2 (显示 SOX2 抗体) repression in TCam-2 cells can be abrogated by recruitment of the constitutively expressed H3K27 demethylase (显示 MBD2 抗体) UTX (显示 KDM6A 抗体) to the SOX2 (显示 SOX2 抗体) promoter through retinoid signaling, leading to expression of neuronal and other lineage genes. SOX17 (显示 SOX17 抗体) has been shown to initiate human PGC (显示 PGC 抗体) specification, with its target PRDM1 suppressing mesendodermal genes
The interaction between c-Maf (显示 MAF 抗体) and RORgammat, and Blimp-1.
these results provide novel clinical and biological insight into the tumor-suppressive role of PRDM1/BLIMP-1 in ABC (显示 ABCB6 抗体)-DLBCL patients and suggest that loss of PRDM1/BLIMP-1 function contributes to the overall poor prognosis of ABC (显示 ABCB6 抗体)-DLBCL patients.
PRDM1 was identified as a susceptibility gene for systemic sclerosis.
Data indicate that BTG2 (显示 BTG2 抗体), MAP3K11 (显示 MAP3K11 抗体), RPS6KA1 (显示 RPS6KA1 抗体) and PRDM1 as putative targets of microRNA miR (显示 MLXIP 抗体)-125b.
we identified MIR155HG and TERC to be transcriptionally downregulated by PRDM1 in two PRDM1-null NK-cell lines when it is ectopically expressed. These findings suggest that ZFAS1 and other dysregulated long non-coding RNAs may be involved in natural killer/T-cell lymphoma pathobiology through regulation of cancer-related genes, and loss-of-PRDM1 expression in natural killer/T-cell lymphomas tumorigenesis
identified the Prdm1 gene encoding the B lymphocyte-induced maturation protein 1 as a crucial negative regulator of human TH17 cell differentiation
B cell receptor signaling component, SYK (显示 SYK 抗体), caused PAX5 (显示 PAX5 抗体) tyrosine phosphorylation in vitro and in cells. Transcriptional repression on the BLIMP1 promoter by PAX5 (显示 PAX5 抗体) was attenuated by this phosphorylation.
Depletion of PRDM1 in lung cancer cells promotes cellular invasion and anoikis resistance in vitro and lung metastasis in vivo.
Data show there was a positive correlation between B cell lymphoma 6 (Bcl-6 (显示 BCL6 抗体)) and B lymphocyte-induced maturation protein 1 (Blimp-1) at the level of mRNA.
Results established a molecular mechanism of TNF-a (显示 TNF 抗体)-induced osteoclasts differentiation, and provided insights into the potential contribution of Blimp1 in the regulation of osteoclastogenesis by TNF-a (显示 TNF 抗体).
results show that the intersection of three or more transcription factors is required to correctly regulate the spatial and temporal features of Blimp1 enhancer expression
findings show that Prdm1 acts independently of Aire (显示 AIRE 抗体), a crucial transcription factor implicated in medullary thymic epithelial cells function; data highlight a previously unrecognized role for Prdm1 in regulating thymic epithelial function
Prdm1 repressed expression of the gene encoding cathepsin S (Ctss (显示 CTSS 抗体)). Prdm1 deficiency in dendritic cells led to loss of appropriate regulation of Ctss (显示 CTSS 抗体) expression in female mice and thereby modulated antigen presentation and the follicular helper T cell repertoire to contribute to autoimmunity in lupus.
Blimp1 is required to maintain a highly proliferative luminal subset necessary for mammary gland development and homeostasis.
Attenuated leptin-receptor (LEPR (显示 LEPR 抗体)) expression is essential for the development and maintenance of acute lymphoblastic leukemia (ALL), and that fasting inhibits ALL development by upregulation of LEPR (显示 LEPR 抗体) and its downstream signaling through the protein PR/SET domain 1 (PRDM1).
role of Blimp-1 as a critical regulator of CD4 (显示 CD4 抗体) dysfunction and links it to the CD8 (显示 CD8A 抗体) T cell dysfunctionality observed in infected mice.
Contextual ablation of BLIMP-1 and p53 (显示 TP53 抗体) led to development of IgM (显示 CD40LG 抗体)-positive B-cell lymphoma with an aggressive phenotype, supported by c-Myc (显示 MYC 抗体) up-regulation, and accumulation of somatic mutations, as demonstrated by whole exome sequencing.
this study shows that IL-10 (显示 IL10 抗体) production during B-cell development is strongly correlated with the expression level of Prdm1
The escape of a fraction of Primordial germ cells from the Prdm1 deletion was sufficient to recover fairly normal germ cell pools, both in male and female adults
This gene encodes a protein that acts as a repressor of beta-interferon gene expression. The protein binds specifically to the PRDI (positive regulatory domain I element) of the beta-IFN gene promoter. Transcription of this gene increases upon virus induction. Two alternatively spliced transcript variants that encode different isoforms have been reported.
PR domain containing 1, with ZNF domain
, Blimp-1 protein
, B lymphocyte-induced maturation protein 1
, PR domain zinc finger protein 1
, PR domain-containing 1
, U boot
, B lymphocyte induced maturation protein 1
, PR domain zinc finger protein 1-like
, B-lymphocyte-induced maturation protein 1
, PRDI-binding factor-1
, beta-interferon gene positive-regulatory domain I binding factor
, B lymphocyte induced maturation protein
, PR domain containing 1 with ZNF domain
, PR domain-containing protein 1
, beta-interferon gene positive regulatory domain I-binding factor