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  人才招聘  關于我們  聯(lián)系我們
欧美精品在线观看,色一情一乱一伦一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ZEB1/NIL2A/HRP Conjugated antibody (bs-4187R-HRP)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-4187R-HRP
英文名稱1 Rabbit Anti-ZEB1/NIL2A/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標記的負調控因子白細胞介素2抗體
別    名 AREB 6; AREB6; BZP; Delta crystallin enhancer binding factor 1; DELTA EF1; FECD6; MGC133261; Negative regulator of IL 2; Negative regulator of IL2; NIL 2 A; NIL 2 A zinc finger protein; NIL 2A; NIL-2-A zinc finger protein; NIL2A; Posterior polymorphous corneal dystrophy 3; PPCD3; Represses interleukin 2 expression; TCF 8; TCF-8; TCF8; Transcription factor 8 (represses interleukin 2 expression); Transcription factor 8; ZEB 1; ZEB; ZEB1; ZEB1_HUMAN; ZFHEP; ZFHX 1A; ZFHX1A; Zinc finger E box binding homeobox 1; Zinc finger E-box-binding homeobox 1; Zinc finger homeodomain enhancer binding protein.  
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  染色質和核信號  信號轉導  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Rat,  (predicted: Mouse, Chicken, Dog, Pig, Cow, Rabbit, )
產品應用 WB=1:500-2000 ELISA=1:100-1000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 124kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZEB1
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.
產品介紹 background:
This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010]

Function:
Acts as a transcriptional repressor. Inhibits interleukin-2 (IL-2) gene expression. Enhances or represses the promoter activity of the ATP1A1 gene depending on the quantity of cDNA and on the cell type. Represses E-cadherin promoter and induces an epithelial-mesenchymal transition (EMT) by recruiting SMARCA4/BRG1. Represses BCL6 transcription in the presence of the corepressor CTBP1. Positively regulates neuronal differentiation. Represses RCOR1 transcription activation during neurogenesis. Represses transcription by binding to the E box (5'-CANNTG-3'). Promotes tumorigenicity by repressing stemness-inhibiting microRNAs.

Subunit:
Interacts (via N-terminus) with SMARCA4/BRG1.

Subcellular Location:
Nucleus.

Tissue Specificity:
Colocalizes with SMARCA4/BRG1 in E-cadherin-negative cells from established lines, and stroma of normal colon as well as in de-differentiated epithelial cells at the invasion front of colorectal carcinomas (at protein level). Expressed in heart and skeletal muscle, but not in liver, spleen, or pancreas.

DISEASE:
Corneal dystrophy, posterior polymorphous, 3 (PPCD3) [MIM:609141]: A subtype of posterior corneal dystrophy, a disease characterized by alterations of Descemet membrane presenting as vesicles, opacities or band-like lesions on slit-lamp examination and specular microscopy. Affected patient typically are asymptomatic. Note=The disease is caused by mutations affecting the gene represented in this entry.
Corneal dystrophy, Fuchs endothelial, 6 (FECD6) [MIM:613270]: A corneal disease caused by loss of endothelium of the central cornea. It is characterized by focal wart-like guttata that arise from Descemet membrane and develop in the central cornea, epithelial blisters, reduced vision and pain. Descemet membrane is thickened by abnormal collagenous deposition. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the delta-EF1/ZFH-1 C2H2-type zinc-finger family.
Contains 7 C2H2-type zinc fingers.
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 396029 Chicken

Entrez Gene: 535183 Cow

Entrez Gene: 6935 Human

Entrez Gene: 21417 Mouse

Entrez Gene: 25705 Rat

Omim: 189909 Human

SwissProt: P36197 Chicken

SwissProt: P37275 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.xucheq.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         京公網安備110107000727號
一个刚拔出来另一个| 人人妻人爽A片二区三区| 女厕厕露P撒尿八个少妇| 久久国产加勒比精品无码| 99蜜桃在线观看免费视频网站 | PPYPP| 重口老太大和小伙乱| 亚洲国产精品无码久久久| 成人综合婷婷国产精品久久蜜臀| 色88久久久久高潮综合影院| 久久久国产精品免费A片3D| 中文字幕AⅤ人妻一区二区| JZZIJZZIJ亚洲成熟少妇 | 一本色道久久综合亚洲精品| 小雪被老外黑人撑破了视频| 狠狠躁18三区二区一区| 天美传媒免费观看一二三在线| 国产亚洲AV综合人人澡精品| WWW.色五月| 浴室人妻的情欲HD三级| 性做爰高清视频在线观看视频| 一次灌浆与二次灌浆| 少妇特黄A片一区二区三区蜜桃| 色综合久久精品亚洲国产 | 久久久久久AV无码免费看大片| 一区二区三区视频| 国产精品久久久久一区二区三区 | 亚洲国产成人精品无码区花野真一| 日日噜噜噜夜夜爽爽狠狠| 妻子4免费完整版中文版| 波多野结AV衣东京热无码专区| 日本不卡三区| 国产成人精品一区二三区| 性做久久久久久| 国产精品福利一区二区| 国产乱老熟妇吃嫩草| 熟妇人妻中文字幕无码老熟妇| 无码AV免费毛片一区二区| 亚洲成AV人片在线观看无 | 国产又色又爽无遮挡免费| 女人做爰全过程免费观看美女|