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
偷拍真实夫妇作爱视频,亚洲精品久久久久AV无码
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-PDX1/Cy3 Conjugated antibody (bs-0923R-Cy3)
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: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-0923R-Cy3
英文名稱1 Rabbit Anti-PDX1/Cy3 Conjugated antibody
中文名稱 Cy3標記的胰島素促進因子/胰十二指腸同源異型盒蛋白抗體
別    名 Glucose sensitive factor; Glucose-sensitive factor; GSF; IDX 1; IDX-1; IDX1; Insulin promoter factor 1; insulin promoter factor 1 homeodomain transcription factor; insulin upstream factor 1; IPF 1; IPF-1; IPF1; Islet/duodenum homeobox 1; Islet/duodenum homeobox-1; IUF 1; IUF-1; IUF1; MODY4; Pancreas/duodenum homeobox 1; Pancreas/duodenum homeobox protein 1; pancreatic and duodenal homeobox P; PDX 1; PDX-1; PDX1; PDX1_HUMAN; Somatostatin transactivating factor 1; Somatostatin-transactivating factor 1; STF 1; STF-1; STF1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  神經(jīng)生物學(xué)  生長因子和激素  轉(zhuǎn)錄調(diào)節(jié)因子  內(nèi)分泌病  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Rat,  (predicted: Human, Mouse, Chicken, Pig, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 30kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PDX1
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 transcriptional activator of several genes, including insulin, somatostatin, glucokinase, islet amyloid polypeptide, and glucose transporter type 2. The encoded nuclear protein is involved in the early development of the pancreas and plays a major role in glucose-dependent regulation of insulin gene expression. Defects in this gene are a cause of pancreatic agenesis, which can lead to early-onset insulin-dependent diabetes mellitus (IDDM), as well as maturity onset diabetes of the young type 4 (MODY4). [provided by RefSeq, Aug 2017]

Function:
Activates insulin, somatostatin, glucokinase, islet amyloid polypeptide and glucose transporter type 2 gene transcription. Particularly involved in glucose-dependent regulation of insulin gene transcription. Binds preferentially the DNA motif 5'-[CT]TAAT[TG]-3'. During development, specifies the early pancreatic epithelium, permitting its proliferation, branching and subsequent differentiation. At adult stage, required for maintaining the hormone-producing phenotype of the beta-cell.

Subunit:
Interacts with the basic helix-loop-helix domains of TCF3(E47) and NEUROD1 and with HMG-I(Y). Interacts with SPOP. Interacts with the methyltransferase SETD7.

Subcellular Location:
Nucleus.

Tissue Specificity:
Duodenum and pancreas (Langerhans islet beta cells and small subsets of endocrine non-beta-cells, at low levels in acinar cells).

Post-translational modifications:
Phosphorylated by the SAPK2 pathway at high intracellular glucose concentration.

DISEASE:
Defects in PDX1 are a cause of pancreatic agenesis (PAC)[MIM:260370]. This autosomal recessive disorder is characterized by absence or hypoplasia of pancreas, leading to early-onset insulin-dependent diabetes mellitus. This was found in a frameshift mutation that produces a truncated protein and results in a second initiation that produces a second protein that act as a dominant negative mutant.
Defects in PDX1 are a cause of non-insulin-dependent diabetes mellitus (NIDDM) [MIM:125853]; also known as diabetes mellitus type 2. NIDDM is characterized by an autosomal dominant mode of inheritance, onset during adulthood and insulin resistance.
Defects in PDX1 are the cause of maturity-onset diabetes of the young type 4 (MODY4) [MIM:606392]; also symbolized MODY-4. MODY is a form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease.

Similarity:
Belongs to the Antp homeobox family. IPF1/XlHbox-8 subfamily.
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 538927 Cow

Entrez Gene: 493994 Dog

Entrez Gene: 3651 Human

Entrez Gene: 18609 Mouse

Entrez Gene: 29535 Rat

Omim: 600733 Human

SwissProt: P52945 Human

SwissProt: P52946 Mouse

SwissProt: P52947 Rat

Unigene: 32938 Human

Unigene: 389714 Mouse

Unigene: 54603 Rat



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

PDX1是一種同源框轉(zhuǎn)錄因子-即胰十二指腸同源異型盒基因,又稱IPF-1(胰島素促進因子)、IDX-1、IUF-1。
近年來,科學(xué)家們對PDX1從不同的角度進行了卓有成效的研究。有學(xué)者認為;PDX1是胰腺發(fā)育及胰島素基因轉(zhuǎn)錄表達的關(guān)鍵性轉(zhuǎn)錄因子,即決定于胰腺前體細胞向B、A、D細胞的分化。
還有學(xué)者認為:PDX1對于腸內(nèi)胚層背胰芽和腹胰芽的生長、分化起重要作用,早期胰腺表達的PDX-1對胰腺上皮的形成和分化是必需的。
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
av片在线播放| 日本护士野外XXXHD| 啊轻点灬太粗嗯太深了用力| 好爽…又高潮了免费毛片| 久久精品国产一区二区电影| 色欲狠狠躁天天躁无码中文字幕| 色欲狠狠躁天天躁无码中文字幕 | 国产精品爱久久久久久久| 亚洲日韩精品欧美一区二区| 成人免费视频一区二区| 全部免费毛片在线播放| 极品尤物一区二区三区| 亚洲AV日韩AV无码| 99好久被狂躁A片视频无码| 香蕉久久久久久AV成人| 久久精品人人做人人爽电影蜜月| 精品少妇人妻AV一区二区三区| 欧美人妻日韩精品| 亚洲欧美日韩在线不卡| 国产精品国产三级国产A| 久久精品国产亚洲7777| 久久精品麻豆日日躁夜夜躁| 日本特黄特色AAA大片免费| 欧美性受XXXX| 无码人妻AⅤ一区二区三区| 蜜桃臀无码内射一区二区三区 | 乳尖乱颤娇喘连连A片在线观看| 特黄A级毛片| 女人扒开屁股桶爽30分钟| 欧美mv日韩mv国产网站| 又大又紧又粉嫩18P少妇| 亚洲AV无码一区二区三区DV| 中国人妻被两个老外三P| 亚洲精品久久AV无码一区二区| 人人爽久久涩噜噜噜AV| 女人下边被添全过视频| 国产在线观看无码免费视频| 无码AV中文一区二区三区桃花岛| 欧美激情性做爰免费视频| 亚洲精华国产精华精华液网站| 男人的好免费观看直播|