强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關(guān)于我們  聯(lián)系我們
黃色一级A一片人与,91精品人妻无码,日本中文字幕在线播放
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-AP2 alpha/PE-Cy7 Conjugated antibody (bs-3569R-PE-Cy7)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-3569R-PE-Cy7
英文名稱 Rabbit Anti-AP2 alpha/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的轉(zhuǎn)錄激活蛋白2α/TFAP2α/AP-2α抗體
別    名 Activating enhancer binding protein 2 alpha; Activating enhancer-binding protein 2-alpha; Activator protein 2; AP 2; AP 2 transcription factor; AP 2alpha; AP-2; AP-2 transcription factor; AP2; AP2 Transcription Factor; AP2-alpha; AP2A_HUMAN; AP2TF; BOFS; Clathrin Adaptor Protein Complex; FLJ51761; TFAP 2; TFAP 2A; TFAP2; TFAP2A; Transcription factor AP 2 alpha (activating enhancer binding protein 2 alpha); Transcription factor AP 2 alpha; Transcription factor AP-2-alpha; Transcription factor AP2 alpha.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 腫瘤  免疫學  信號轉(zhuǎn)導  細胞凋亡  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 48kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human AP2 alpha
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹 background:
The protein encoded by this gene is a transcription factor that binds the consensus sequence 5'-GCCNNNGGC-3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS). Three transcript variants encoding different isoforms have been found for this gene.

Function:
Sequence-specific DNA-binding protein that interacts with inducible viral and cellular enhancer elements to regulate transcription of selected genes. AP-2 factors bind to the consensus sequence 5'-GCCNNNGGC-3' and activate genes involved in a large spectrum of important biological functions including proper eye, face, body wall, limb and neural tube development. They also suppress a number of genes including MCAM/MUC18, C/EBP alpha and MYC. AP-2-alpha is the only AP-2 protein required for early morphogenesis of the lens vesicle. Together with the CITED2 coactivator, stimulates the PITX2 P1 promoter transcription activation. Associates with chromatin to the PITX2 P1 promoter region.

Subunit:
Binds DNA as a dimer. Can form homodimers or heterodimers with other AP-2 family members. Interacts with WWOX. Interacts with CITED4. Interacts with UBE2I. Interacts with RALBP1 in a complex also containing EPN1 and NUMB during interphase and mitosis. Interacts with KCTD1; this interaction represses transcription activation. Interacts (via C-terminus) with CITED2 (via C-terminus); the interaction stimulates TFAP2A-transcriptional activation. Interacts (via N-terminus) with EP300 (via N-terminus); the interaction requires CITED2.

Subcellular Location:
Nucleus.

Post-translational modifications:
Sumoylated on Lys-10; which inhibits transcriptional activity (Probable).

DISEASE:
Branchiooculofacial syndrome (BOFS) [MIM:113620]: A syndrome characterized by growth retardation, bilateral branchial sinus defects with hemangiomatous, scarred skin, cleft lip with or without cleft palate, pseudocleft of the upper lip, nasolacrimal duct obstruction, low set ears with posterior rotation, a malformed, asymmetrical nose with a broad bridge and flattened tip, conductive or sensorineural deafness, ocular and renal anomalies. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the AP-2 family.

Database links:

Entrez Gene: 7020 Human

Entrez Gene: 21418 Mouse

Entrez Gene: 306862 Rat

Omim: 107580 Human

SwissProt: P05549 Human

SwissProt: P34056 Mouse

SwissProt: P58197 Rat

Unigene: 519880 Human

Unigene: 85544 Mouse

Unigene: 22545 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

轉(zhuǎn)錄因子AP-2α在哺乳動物發(fā)育、分化以及腫瘤的發(fā)生等生命現(xiàn)象中起重要作用.
版權(quán)所有 2004-2026 www.nmgps.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
乡村少妇被躁得白浆直流91 | japanese极品丰满少妇 | 福利中文弹幕在线观看 | 国产精品久久久久AV | 美国A级毛片免费视频 | 日本黄色视频免费看 | 性感成熟动漫美女在线观看一区二区的 | 日本乱偷中文字幕 | 精品国产无码在线观看 | 特级西西444www无码视频免费看 | EEUSS鲁丝片无码入口 | 久久无码人妻一区二区三区午夜免费 | 青娱乐性爱视频网站 | 无码人妻精品一区二区二秋霞影院 | 国产无人区一区二区三区四区 | 中文字幕无码A片一区在线观看 | 久久人人妻人人人人妻性色aV | 蜜桃亚洲AV啪啪无码片 | 国产精品久久久久久无码欧美内衣 | 黄色视频在线观看无码免费 | 韩国无码成人三区在线观看 | 亚洲中文字幕A V奸 蜜桃av网站在线浏览 | 无码人妻精品一区二区三区潘金莲 | 免费无码婬片AAAA在线观看 | 久久精品久久久精品美女 | 美女裸体网站熟女一区 | 精品动漫3D一区二区三区免费版 | 红桃视频成人版黄A片 | 又粗又长的一区二区 | 四虎成人免费视频在线观看 | 亚洲欧洲精品mv免费看 | 欧美熟妇另类久久久久久久 | 三人成全视频在线观看免费 | 日韩无码高清视频 | 亚洲国产高清无码视频 | 虎色视频成人版免费 | 中文字幕丰满人妻无码区隔壁人爱 | 四川少妇BBBBBB爽爽电影 | 专干老熟女600部 | 中文本幕 的搜索结果 - 91n | 人人添人人澡久久婷亚洲AV |