99精品欧美一区二区三区综合在线,国产精品一区二区的,欧美亚洲国产日韩综合,99精品视频在线观看2

掃碼關(guān)注公眾號(hào)           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
久久久精品久久久精品,欧美三级黄片在线观看,精品人妻码一区二区三区剧情
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
PDX1 Rabbit pAb (bs-20738R)  
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.eweiwc.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.eweiwc.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)

產(chǎn)品編號(hào) bs-20738R
英文名稱 PDX1 Rabbit pAb
中文名稱 胰島素促進(jìn)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_HUMAN; Somatostatin transactivating factor 1; Somatostatin-transactivating factor 1; STF 1; STF-1; STF1.  
研究領(lǐng)域 細(xì)胞生物  神經(jīng)生物學(xué)  生長(zhǎng)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) Human,Mouse,Rat (predicted: Rabbit,Pig,Sheep,Cow,Chicken,Dog,Horse)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,Flow-Cyt=1μg/Test
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 30 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PDX1: 101-200/284 
亞    型 IgG
純化方法 affinity purified by Protein A
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(xiàng) 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 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.

SWISS:
P52945

Gene ID:
3651

Database links:

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



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(jìn)因子)、IDX-1、IUF-1。
近年來,科學(xué)家們對(duì)PDX1從不同的角度進(jìn)行了卓有成效的研究。有學(xué)者認(rèn)為;PDX1是胰腺發(fā)育及胰島素基因轉(zhuǎn)錄表達(dá)的關(guān)鍵性轉(zhuǎn)錄因子,即決定于胰腺前體細(xì)胞向B、A、D細(xì)胞的分化。
還有學(xué)者認(rèn)為:PDX1對(duì)于腸內(nèi)胚層背胰芽和腹胰芽的生長(zhǎng)、分化起重要作用,早期胰腺表達(dá)的PDX-1對(duì)胰腺上皮的形成和分化是必需的。
產(chǎn)品圖片
Paraformaldehyde-fixed, paraffin embedded (rat pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; A
Paraformaldehyde-fixed, paraffin embedded (mouse pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min;
Blank control (blue line): Hep G2 (fixed with 70% ethanol (Overnight at 4℃) and then permeabilized with 90% methanol for 20 min at -20℃). Primary Antibody (green line): Rabbit Anti-PDX1 antibody (bs-20738R),Dilution: 0.2μg /10^6 cells. Isotype Control
版權(quán)所有 2004-2026 www.www.eweiwc.cn 北京博奧森生物技術(shù)有限公司
通過國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
中日韩VA无码中文字幕| 国内揄拍国内精品| a一级毛片免费高清在线| 欧美一区亚洲一区视频在线观看| 午夜性福福利视频一区二区三区| 亚洲欧洲精品无码久久久| 白丝袜子宫啊啊啊不要了| 日韩欧美综合一二三区| 免费国产香蕉视频在线观看| 久久久久精品无码专区喝奶| 男人草女人的骚逼逼| 久久国产精品二卡| 尤物AV无码国产在线看| 日韩欧美一区二三区风间由美| 亚洲欧美日韩另类| 欧美一区二区三区久久国产精品| 午夜场射精嗯嗯啊啊视频| 操大美女逼射精视频| 久久免费国产视频| 国产天堂网一区二区三区 | 激情亚洲人妻精品| 午夜精品在线视频| 影音先锋天堂网亚洲无码| 免费黄色 操逼视频| 美女的粉嫩小逼视频特写| 亚洲一区二区女同性恋免费看| 九热中文字幕在线| 淫荡淫水逼操烂视频| 日本成人在线一区中文字幕| 我要操日本女人的逼| 国产伦精品一区二区三区视频抖音| 东京热无码AV一区二区三区| 被春药女高潮抽搐喷水视频| 国产伦精品一区二区三区视频抖音| 免费人成再在线观看| 91秦先生全集在线观看| 国产亚洲一区白丝在线观看| 二次元男生操女生屁眼爽| 无码人妻丰满熟妇区精品| 青娱乐欧美性爱视频| 欧美一区二区三区高清性群p|