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
特大黑人与亚洲娇小,处破女轻点疼丨98分钟,翁与小莹浴室欢爱52章
Rabbit Anti-HESX1/FITC Conjugated antibody (bs-13597R-FITC)
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-13597R-FITC
英文名稱1 Rabbit Anti-HESX1/FITC Conjugated antibody
中文名稱 FITC標(biāo)記的同源結(jié)構(gòu)域轉(zhuǎn)錄因子HESX1抗體
別    名 HESX1_HUMAN; Homeobox expressed in ES cells 1; Homeobox protein ANF; hAnf.   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 免疫學(xué)  神經(jīng)生物學(xué)  干細(xì)胞  轉(zhuǎn)錄調(diào)節(jié)因子  細(xì)胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 21kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HESX1
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 homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.

Function:
Homeobox protein expressed in embryonic stem cells and targetd by Sox2, Oct4 and Nanog. Required for the normal development of the forebrain, eyes and other anterior structures such as the olfactory placodes and pituitary gland. Possible transcriptional repressor.

Subunit:
Can form heterodimers with PROP1 in binding to DNA. Interacts with TLE1.

Subcellular Location:
Nuclear

DISEASE:
Septooptic dysplasia (SOD) [MIM:182230]: A clinically heterogeneous disorder defined by any combination of optic nerve hypoplasia, pituitary gland hypoplasia with panhypopopituitarism, and midline abnormalities of the brain, including absence of the corpus callosum and septum pellucidum. Note=The disease is caused by mutations affecting the gene represented in this entry.
Growth hormone deficiency with pituitary anomalies (GHDPA) [MIM:182230]: A disease characterized by low or absent growth hormone levels, in the presence of a hypoplastic anterior pituitary lobe and ectopic or absent posterior pituitary lobe. Note=The disease is caused by mutations affecting the gene represented in this entry.
Pituitary hormone deficiency, combined, 5 (CPHD5) [MIM:182230]: Combined pituitary hormone deficiency is defined as the impaired production of growth hormone and one or more of the other five anterior pituitary hormones. CPHD5 is characterized by complete or partial deficiencies of growth hormone, thyroid-stimulating hormone, luteinizing hormone, follicle stimulating hormone and adrenocorticotropic hormone. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the ANF homeobox family.
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 8820 Human

Omim: 601802 Human

SwissProt: Q52LC5 Human

SwissProt: Q9UBX0 Human

Unigene: 171980 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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
小莹乳液汁水停电了还能用吗| 久久夜色精品国产欧美乱| 精品国产AV一区二区三区| 国产偷v国产偷v亚洲高清| 国产午夜精品一区二区三区| 久久www香蕉免费人成| 国模吧| 丰满多毛的大隂户视频 | 无码国产精品一区二区免费16| 粉嫩XB粉嫩XB粉嫩XB| 精品无码三级在线观看视频| 男JI大巴进入女人的视频| 999久久久免费精品国产| 中文字幕乱码人妻一区二区三区 | 精品国产AV久久久久无码 | 亚洲成A人V欧美综合天堂麻豆| FREE性玩弄少妇HD| 亚婷婷洲AV久久蜜臀无码| 亚洲国产精品日韩AV不卡在线| 又大又长粗又爽又黄少妇视频| 国产精品ⅴ无码大片在线看| 狠狠色噜噜狠狠狠888米奇视频 | 欧美人与动性XXXXX杂性| 久久夜色精品国产噜噜亚洲AV| 欧美日韩成人在线| 后入内射无码人妻一区| 国产精品内射后入合集 | 大屁股熟女一区二区三区| 18禁男女爽爽爽午夜网站免费| 蜜桃人妻无码AV天堂三区| 少妇高潮惨叫久久久久久| 五月丁香啪啪| 青柠在线影院观看日本| 亚洲精品乱码久久久久久| 亚洲AV午夜成人片精品网站| 老同学3免费完整版在线观看| 国产男女猛烈无遮挡免费视频网站| 亚洲日韩精品一区二区三区无码| 亚洲成AV人片在线观看| AAAAA级少妇高潮大片免费看| 女人18毛片水真多|