吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
西西里的美丽传说在线观看,成人免费毛片AAAAAA片
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Mouse Anti-BCL-6  antibody (bsm-51096M)  
~~~促銷代碼KT202411~~~
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說明書: 50ul  100ul  
50ul/1580.00元
100ul/2500.00元
大包裝/詢價
產(chǎn)品編號 bsm-51096M
英文名稱 Mouse Anti-BCL-6  antibody
中文名稱 Bcl-6單克隆抗體
別    名 B-Cell CLL/Lymphoma 6; Zinc Finger Protein 51; Zinc Finger And BTB Domain-Containing Protein 27; B-Cell Lymphoma 5 Protein; Protein LAZ-3; ZBTB27; ZNF51; BCL-5; BCL-6; BCL5; LAZ3; Lymphoma-Associated Zinc Finger Gene On Chromosome 3; Cys-His2 Zinc Finger Transcription Factor; Zinc Finger Transcription Factor BCL6S; B-Cell Lymphoma 6 Protein Transcript; B-Cell Lymphoma 6 Protein; BCL6A; BCL6_HUMAN;   
研究領(lǐng)域 腫瘤  免疫學(xué)  信號轉(zhuǎn)導(dǎo)  細(xì)胞凋亡  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 6F5
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 WB=1:500-5000,ELISA=1:500-5000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 78kDa
細(xì)胞定位 細(xì)胞核 
性    狀 Liquid
濃    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human BCL-6: 676-704/706 
亞    型
純化方法 affinity purified by Protein G
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal POZ domain. This protein acts as a sequence-specific repressor of transcription, and has been shown to modulate the transcription of STAT-dependent IL-4 responses of B cells. This protein can interact with a variety of POZ-containing proteins that function as transcription corepressors. This gene is found to be frequently translocated and hypermutated in diffuse large-cell lymphoma (DLCL), and may be involved in the pathogenesis of DLCL. Alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Aug 2015]

Function:
Transcriptional repressor mainly required for germinal center (GC) formation and antibody affinity maturation which has different mechanisms of action specific to the lineage and biological functions. Forms complexes with different corepressors and histone deacetylases to repress the transcriptional expression of different subsets of target genes. Represses its target genes by binding directly to the DNA sequence 5-TTCCTAGAA-3 (BCL6-binding site) or indirectly by repressing the transcriptional activity of transcription factors. In GC B-cells, represses genes that function in differentiation, inflammation, apoptosis and cell cycle control, also autoregulates its transcriptional expression and up-regulates, indirectly, the expression of some genes important for GC reactions, such as AICDA, through the repression of microRNAs expression, like miR155. An important function is to allow GC B-cells to proliferate very rapidly in response to T-cell dependent antigens and tolerate the physiological DNA breaks required for immunglobulin class switch recombination and somatic hypermutation without inducing a p53/TP53-dependent apoptotic response. In follicular helper CD4(+) T-cells (T(FH) cells), promotes the expression of T(FH)-related genes but inhibits the differentiation of T(H)1, T(H)2 and T(H)17 cells. Also required for the establishment and maintenance of immunological memory for both T- and B-cells. Suppresses macrophage proliferation through competition with STAT5 for STAT-binding motifs binding on certain target genes, such as CCL2 and CCND2. In response to genotoxic stress, controls cell cycle arrest in GC B-cells in both p53/TP53-dependedent and -independent manners. Besides, also controls neurogenesis through the alteration of the composition of NOTCH-dependent transcriptional complexes at selective NOTCH targets, such as HES5, including the recruitment of the deacetylase SIRT1 and resulting in an epigenetic silencing leading to neuronal differentiation.

Subunit:
Homodimer. Interacts (via BTB domain) with the corepressors BCOR, NCOR1 and SMRT/NCOR2; the interactions are direct. Forms preferably ternary complexes with BCOR and SMRT/NCOR2 on target gene promoters but, on enhancer elements, interacts with SMRT/NCOR2 and HDAC3 to repress proximal gene expression. Interacts with histone deacetylases HDAC2, HDAC5 and HDAC9 (via the catalytic domain). Interacts with ZBTB7 and BCL6B. Interacts with SCF(FBXO11) complex; the interaction is independent of phosphorylation and promotes ubiquitination. Interacts (when phosphorylated) with PIN1; the interaction is required for BCL6 degradation upon genotoxic stress. Interacts with ZBTB17; inhibits ZBTB17 transcriptional activity. Interacts with CTBP1, autoinhibits its transcriptional expression. Interacts with NOTCH1 NCID and SIRT1; leads to a epigenetic repression of selective NOTCH1-target genes. Interacts (nor via BTB domain neither acetylated) with the NuRD complex components CHD4, HDAC1, MBD3 and MTA3; the interaction with MTA3 inhibits BCL6 acetylation and is required for BCL6 transpriptional repression.

Subcellular Location:
Nucleus

Tissue Specificity:
Expressed in germinal center T- and B-cells and in primary immature dendritic cells.

Post-translational modifications:
Phosphorylated by MAPK1 in response to antigen receptor activation at Ser-333 and Ser-343. Phosphorylated by ATM in response to genotoxic stress. Phosphorylation induces its degradation by ubiquitin/proteasome pathway.
Polyubiquitinated. Polyubiquitinated by SCF(FBXO11), leading to its degradation by the proteasome.
Acetylated at Lys-379 by EP300 which inhibits the interaction with NuRD complex and the transcriptional repressor function. Deacetylated by HDAC- and SIR2-dependent pathways.

SWISS:
P41182

Gene ID:
604

Database links:

Entrez Gene: 604 Human

Entrez Gene: 12053 Mouse

Entrez Gene: 303836 Rat

Omim: 109565 Human

SwissProt: P41182 Human

SwissProt: P41183 Mouse

Unigene: 478588 Human

Unigene: 347398 Mouse

Unigene: 20571 Rat



版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網(wǎng)安備110107000727號
无码专区AAAAAA免费视频| 久久久久免费毛A片免费一瓶梅| 欧美精品一区二区少妇免费A片| 最近中文字幕在线看免费完整版| 99精品一区二区三区无码吞精| 新岳乱合集500系列| 久久久久久久久波多野高潮| 欧美变态口味重另类在线视频 | 无码人妻AⅤ一区二区三区| 国产FREEXXXX性播放麻豆| 免费特级毛片| 日韩精品久久久久久免费| 精品视频一区二区三区在线观看| 亚洲精品国偷拍自产在线观看蜜臀| 久久精品AⅤ无码中文字字| 国产男女爽爽爽免费视频| 丰满人妻一区二区三区免费视频| 国产精品久久久久久久久久久不卡| 花房姑娘免费观看全集| 一本一道AV无码中文字幕| 亚VA芒果乱码一二三四区别| 精品无码三级在线观看视频| 欧美熟妇VIVOE精品| 豆国产97在线 | 亚洲| 成人无码精品1区2区3区免费看| 久久久久久久女国产乱让韩| 狠狠在啪线香蕉777视频| 中文无码熟妇人妻AV在线| 国产精品久久久久久妇女| 精品爆乳一区二区三区无码AV| 性高湖久久久久久久久| 99精品国产一区二区| 亚洲精品无码久久久久久| 午夜福利一区二区三区在线观看| 国产A√精品区二区三区四区| 小SAO货水好多真紧H无码视频| 高清欧美性猛交XXXX黑人猛交| 99精品视频在线观看免费| 新岳乱合集500系列| 少妇扒开粉嫩小泬视频| 亚洲H在线播放在线观看H|