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
掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
寡妇高潮一级毛片免费看,无码人妻一区二区三区线花季传件
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-AP2 alpha/BF555 Conjugated antibody (bs-3569R-BF555)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-3569R-BF555
英文名稱 Rabbit Anti-AP2 alpha/BF555 Conjugated antibody
中文名稱 BF555標記的轉錄激活蛋白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  
研究領域 腫瘤  免疫學  信號轉導  細胞凋亡  轉錄調節(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.
版權所有 2004-2026 m.nmgps.com 北京博奧森生物技術有限公司
通過國際質量管理體系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
东北少妇大叫高潮XXXⅩ传媒 | 91精品国产综合一区二区三区大 | 影音先锋每日资源第一页 | 91一区二区三区在线观看 | 亚洲最新国语黄色网址 | 免费看A片奶出水 | 久98久在线观看视频 | 又大又粗又硬又爽又黄视频 | 四川少妇BBB搡BBB爽爽爽视頻 | 国产精品久久久久久无码人妻 | 无码精品一区二区三区四区爱奇艺 | 国产亚无精久久久久久无码 | 小香蕉啪啪午夜成人AV | 少妇性BBB搡BBB爽爽爽视頻 | 中文字幕无码永久无线无码蜜桃视频 | ,四川少妇搡BBBB搡BBBB | 国产男女无套 观看91 | 搡BBBB 搡BBB小说图 | 亚洲天堂国产精品 | 亚洲无 码A片在线观看 | 亚洲中文在线视频 | 无码 白浆 高潮 免费 | 美女黄色视频免费观看 | 国产成人精品免高潮在线观看 | 成人黄色A片免费视频 | 不要,不要黄色成人视频免费观看 | 特级毛片电影免费免费看不收钱 | 扒开腿挺进肉嫩小泬喷水网站 | 欧美丰满熟妇BBBBBB禁忌 | 国产互换人妻XXXX69张雅丹 | 少妇又紧又色又爽又刺激视频 | 国产精品久久久久久一级毛片 | 国产亚洲分享在线视频 | 国产BBB搡BBB爽爽爽 | 搡老女人老妇女老熟女60 | 精品人妻无码一区二区 | 亚洲精品AAAA乱码 | 日本无码一区二区三三 | 精品一区二区三区久久 | 国产一级一级毛片 | 夜夜春亚洲嫩草直播蜜桃 |